The identification of functionally important residues is an important challenge for understanding the molecular mechanisms of proteins. Membrane protein transporters operate two-state allosteric conformational changes using functionally important cooperative residues that mediate long-range communication from the substrate binding site to the translocation pathway. In this study, we identified functionally important cooperative residues of membrane protein transporters by integrating sequence conservation and co-evolutionary information. A newly derived evolutionary feature, the co-evolutionary coupling number, was introduced to measure the connectivity of co-evolving residue pairs and was integrated with the sequence conservation score. We tested this method on three Major Facilitator Superfamily (MFS) transporters, LacY, GlpT, and EmrD. MFS transporters are an important family of membrane protein transporters, which utilize diverse substrates, catalyze different modes of transport using unique combinations of functional residues, and have enough characterized functional residues to validate the performance of our method. We found that the conserved cores of evolutionarily coupled residues are involved in specific substrate recognition and translocation of MFS transporters. Furthermore, a subset of the residues forms an interaction network connecting functional sites in the protein structure. We also confirmed that our method is effective on other membrane protein transporters. Our results provide insight into the location of functional residues important for the molecular mechanisms of membrane protein transporters.
Major Facilitator Superfamily (MFS) transporters are one of the largest families of membrane protein transporters and are ubiquitous to all three kingdoms of life. Structural studies of MFS transporters have revealed that the members of this superfamily share structural homology; however, due to weak sequence similarity, their structural similarity has only been found after structural determination. Even after the structures were solved, painstaking efforts were needed to detect functionally important residues. The identification of functionally important cooperative residues from sequences may provide an alternative way to understanding the function of this important class of proteins. Here, we show that it is possible to identify functionally important residues of MFS transporters by integrating two different evolutionary features, sequence conservation and co-evolutionary information. Our results suggest that the conserved cores of evolutionarily coupled residues are involved in specific substrate recognition and translocation of membrane protein transporters. Also, a subset of the identified residues comprises an interaction network connecting functional sites in the protein structure. The ability to identify functional residues from protein sequences may be helpful for locating potential mutagenesis targets in mechanistic studies of membrane protein transporters.
Citation: Jeon J, Yang J-S, Kim S (2009) Integration of Evolutionary Features for the Identification of Functionally Important Residues in Major Facilitator Superfamily Transporters. PLoS Comput Biol 5(10): e1000522. https://doi.org/10.1371/journal.pcbi.1000522
Editor: Ruth Nussinov, National Cancer Institute, United States of America and Tel Aviv University, Israel
Received: March 10, 2009; Accepted: August 27, 2009; Published: October 2, 2009
Copyright: © 2009 Jeon et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the POSTECH Core Research program, the Korea Science and Engineering Foundation grant (M10753020006-07N5302-00610 and R01-2007-000-20425-0) and the World Class University program (R31-2008-000-10100-0). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The identification of functionally important cooperative residue is important for understanding the allosteric pathways of proteins. Cooperative residues are responsible for long-range allosteric communication from the substrate binding sites to the translocation pathways of membrane protein transporters . A number of methods have been proposed for the identification of functionally important residues in proteins. Based on the notion that functionally important residues tend to be conserved within a protein family ,, sequence conservation analyses have been applied to identify specific functional sites, such as substrate/ligand binding residues , protein-protein interfaces , active sites of enzymes , and residues responsible for functional specificity . Meanwhile, co-evolutionary analyses, which were introduced by the observation that functionally important residues are likely to co-evolve with other functional residues to reduce the effects of mutations , have been applied to identify energetically and/or evolutionarily coupled interactions between the domains of complex proteins , the interaction sites of protein complexes , and the allosteric pathways of proteins ,. One drawback of these approaches is that residues may be conserved or co-evolved due to several underlying causes, such as the maintenance of protein structure, interaction, and folding, as well as functional constraint ,. Therefore, a method that can quantify and detect functional constraints from the evolutionary information in protein sequences would greatly aid the identification of functionally important residues in proteins .
Membrane protein transporters are involved in two-state allosteric communication, which mediates the propagation of regulatory information from the substrate binding site to the translocation pathway through large conformational changes . These conformational changes could be brought about through cooperative residues . Recent studies have suggested that cooperative residues are conserved  or evolutionary coupled  to maintain allosteric communication. Furthermore, it has been proposed that co-evolved pairs of moderately conserved residues are important for protein function . Thus, it may be possible to combine sequence conservation and co-evolutionary analyses to identify the cooperative residues of membrane protein transporters. To do this, we derived a new method for identifying the cooperative residues of membrane protein transporters by integrating two different evolutionary features. We extracted functional information from multiple evolutionary constraints based on the following deduction: we took advantage of the fact that clusters of cooperative residues might be co-evolutionary connected not only by proximal but also distal residues in order to mediate allosteric communication . When we considered a protein as a co-evolving network of residues, high connectivity described the functional essentiality of a single residue. Based on these, we hypothesized that cooperative residues lining the substrate binding and translocation pathway are likely to be conserved and have more co-evolutionarily coupled partners than non-functional residues, showing high connectivity in a co-evolution network. To test our hypothesis, we introduced a co-evolutionary coupling number (CN) to measure the connectivity of co-evolving residue pairs in a co-evolution network. We then integrated CN with sequence conservation score and investigated the functional roles and structural positions of the conserved cores of co-evolutionarily coupled residues.
We initially applied our method to the MFS transporters, LacY, GlpT, and EmrD, for which crystal structures have been solved and whose functional residues have been characterized well enough to evaluate the performance of our method. MFS transporters represent one of the largest and most diverse superfamily of membrane protein transporters and are ubiquitous to all three kingdoms . The identification of cooperative residues of MFS transporters may be helpful in inferring their allosteric mechanisms, including substrate recognition and translocation. MFS transporters move various substrates (e.g., sugar, drug, metabolites, and anions) in different directions across cell membranes using a unique combination of residues in their transmembrane regions . One MFS transporter, lactose permease (LacY), is a symporter that catalyzes the coupled translocation of lactose and H+ . Another, glycerol-3-phosphate transporter (GlpT), mediates the exchange of glycerol-3-phosphate and inorganic phosphate in an antiport manner . Multi-drug transporter, EmrD, is an antiporter that exports a diverse group of chemically unrelated drugs . Using our method, we found that conserved cores of evolutionarily coupled residues comprise residue interaction networks connecting the specific substrate recognition site and translocation pathway of MFS transporters. We also tested our method on other proteins and confirmed that it is effective in identifying the cooperative residues of membrane protein transporters.
Evolutionary constraints on the central cavity of MFS transporters
We devised a new evolutionary feature, co-evolutionary coupling number (CN), and integrated it with the sequence conservation score to select functionally important cooperative residues from protein sequences. Figure 1 diagrams the proposed method. First, we measured co-evolution and sequence conservation scores from homologue sequences. Second, we formulated the CN by counting the number of co-evolving residue pairs per residue. Finally, we calculated a quantitative integration score (IS) of each residue by multiplying sequence conservation score and CN (see Materials and Methods for details).
(A) A schematic view of multiple sequence alignment (MSA) of a protein family. Co-evolution and sequence conservation scores were calculated from homologue sequences. X and Y indicate different residues in a protein. (B) Quantification of the co-evolutionary relationship of a single residue. Co-evolutionary coupling number (CN) was defined by the number of co-evolved residue pairs per residue. A dashed line represents co-evolving residue pairs. Circles represent the co-evolved partners of residues X and Y. (C) Measurement of sequence conservation scores of residues X and Y. Blue and red squares indicate conserved amino acids of residues X and Y, respectively. (D) Normalization of CN and sequence conservation scores by assigning a score raging from 0 to 1. (E) Integration score (IS) was obtained by multiplying CN and sequence conservation score.
To examine whether functionally important cooperative residues tend to be conserved and have many co-evolved partners, we compared average IS, CN, and sequence conservation scores between central cavity residues and non-cavity residues. The central cavity of an MFS transporter is mainly composed of functionally important residues that are involved in substrate recognition and are located in the pathway of substrate transport . We found that central cavity residues were significantly more conserved and had many more co-evolved partners than non-cavity residues, resulting in a high IS (Table S1). The average IS of central cavity residues was 3.1 times higher than that of the non-cavity residues (p-value = 2.31×10−11). Statistical significance was determined by Student's t-test comparing IS distributions between central cavity and non-cavity residues. We further examined the sequence conservation scores of central cavity residues to confirm our initial assumption that central cavity residues are conserved and evolutionary coupled. From the sliding-window analysis of conservation scores, we found that central cavity residues slowly evolved rather than being completely conserved (Figure S1). Central cavity residues were enriched between the 75th and 90th percentile of sequence conservation scores. The fraction of central cavity residues was sharply reduced after the 90th percentile of sequence conservation. These results suggest that a slow evolution rate allows central cavity residues to be conserved and co-evolutionarily coupled with other residues . Therefore, the integration of sequence conservation and CN can be used to identify central cavity residues.
To measure the sensitivity of the integrated evolutionary information, we compared our ability to detect central cavity residues by IS, CN, co-evolution, and sequence conservation scores. We examined the fraction of central cavity residues using various percentile cutoffs for IS, CN, co-evolution, and sequence conservation scores. In comparison to the conventional evolutionary approaches, we found IS to be a more effective way to select central cavity residues. As shown in Figure 2A, IS detected 1.1 to 2.2 times more central cavity residues than CN, co-evolution, or sequence conservation score. We also observed that CN had a higher sensitivity for detecting central cavity residues than co-evolution and sequence conservation. This suggests that central cavity residues tend to be co-evolutionarily coupled with many residues rather than being highly conserved.
(A) Fraction of central cavity residues at the given percentile of each evolutionary approach. Red, green, blue, and yellow squares indicate the average fraction of central cavity residues at the given percentile of IS, CN, co-evolution, and sequence conservation scores, respectively. Error bars indicate the standard deviation. (B) Precision-recall curves of four evolutionary approaches. Precision and recall were derived from cavity residues (positive set) and non-cavity residues (negative set) of three MFS transporters. Red, green, blue, and yellow dots represent the average precision of each evolutionary approach in the given recall. (C) Optimization of the percentile cutoff of IS. False-positive rates of IS were shown at the given percentile cutoffs. The dashed line indicates the percentile cutoff of IS with 5% false-positive rate. Error bars indicate the standard deviation between false-positive rates of three different MFS transporters.
We compared the precision-recall characteristics of IS, CN, co-evolution, and sequence conservation for a more comprehensive evaluation (i.e. how well each of the four approaches do in identifying the central cavity residues). We found that IS was best in the detection of central cavity residues (Figure 2B). Specifically, IS achieved an average precision of 71%, whereas the other evolutionary approaches achieved an average precision of 64% (CN), 58% (co-evolution), and 49% (sequence conservation) at 30% recall. Also, the precision of IS was 3.2-fold higher than a randomly generated set at the same recall. Furthermore, the likelihood ratio of IS was the highest among all four evolutionary approaches (Figure S2). These results indicate that IS can capture the maximum evolutionary property of central cavity residues that would not be apparent by co-evolution or sequence conservation alone.
For the sensitive detection of functional residues, we optimized the percentile cutoff of IS by examining the false-positive rate, which is the fraction of non-cavity residues selected at the given percentile cutoff. We found that, in all three MFS transporters, the 90th percentile of IS discriminated central cavity residues from non-cavity residues with an acceptable false- positive rate of 5% (Figure 2C). Therefore, we used the 90th percentile of IS as a cutoff value to select functional residues for further analyses.
Identification of the cavity residues of LacY
LacY facilitates the transport of lactose through the inner membrane . LacY is an intensively studied protein of the MFS transporters and its functional residues have been well characterized through mutagenesis .
To investigate whether the high-IS residues are involved in substrate binding and translocation, we identified 25 residues within the 90th percentile of IS (Figure 3A) and found that most residues detected at this cutoff have known functional roles (Table 1). The detected residues were mostly positioned within the substrate translocation pathway of the central cavity (Figure 3B). When we mapped the 25 detected residues on the LacY structure, we found that 17 residues (68% of detected residues) were located in the central cavity (Figure 3C and Table S2). It has been experimentally confirmed that six residues, E126, R144, E269, R302, H322, and E325, are irreplaceable and necessary for LacY operation ,, and we detected five of these residues (Figure 3C, shown in bold). We were able to detect E126, R144, R302, H322, and E325, but missed E269 in the 90th percentile of IS. Meanwhile, the missed residue E269 was found in the 70th percentile of IS.
(A) IS pattern of LacY. Black line corresponds to the 90th percentile of IS. Transmembrane regions are indicated as helices below the x-axis with boundary residue numbers; 25 detected residues are labeled with residue numbers. (B) Serial sections of LacY structure from cytoplasm (−15Å) to periplasm (15Å). The detected residues are shown as vdW spheres with residue numbers; 5 irreplaceable residues are shown in bold. (C) ‘Open book’ view of the detected residues in LacY. Central cavity and non-cavity residues are shown in red and blue sticks, respectively; five irreplaceable residues are indicated as bold characters. Transmembrane helix numbers are shown in roman numerals.
Residue interaction network is important for the substrate transport mechanism
Proteins use residue-residue interactions to propagate regulatory information from one functional site to another . We constructed an interaction network by examining the interatomic connectivity among the detected residues. Different types of interactions, such as hydrogen bonds, salt bridges, and van der Waals interactions were assessed by measuring solvent-accessible surface and interatomic distances from the structures of MFS transporters (see Materials and Methods for details). We observed that 23 of the 25 detected residues form an interaction network and 18 of these comprise a main network in the LacY structure (PDB ID: 2CFQ) (Table S3). Of the 18 residues, 15 are central cavity residues known to be essential for LacY operation and 5 of the 18 are irreplaceable (Figure 4A). Hydrogen bonds and salt bridges formed between the residues of Y236, D240, R302, K319, H322, and E325 (bold line in Figure 4A) are known to play important roles in the transduction of the substrate binding signal through the LacY structure ,. Two irreplaceable residues, E126 and R144, found interact through a hydrogen bond, are involved in substrate binding and release .
(A) Interaction network of the detected residues in LacY. Eighteen of the detected residues comprised a main interaction network (left), which can be divided into two sub-networks. Red circle represents central cavity residues and blue circle indicates non-cavity residues. Dashed line indicates a van der Waals interaction. Bold line indicates a potential hydrogen bond or salt bridge. (B) Functional implications of the detected residues from the mutational analyses.
The functional implications of the interaction network are in accordance with the lactose transport mechanism proposed from LacY mutation experiments . Our main network could be divided into two sub-networks based on orientation: network 1 is located on the periplasmic side and network 2 on the cytoplasmic side (Figure 4A). There is evidence that the residues of both sub-networks simultaneously mediate substrate translocation from opposite sides of the membrane (Figure 4B). Residue E325 detects protonation states and transports H+ with R302 and H322 on the periplasmic side, and P327 on the cytoplasmic side . Substrate translocation is mediated by residues Y236, D240, F261, G262, and M299 of network 1 and residues A273 and M276 of network 2 –. Residues K319 in network 1 and G147 in network 2 are involved in substrate accumulation . Among the residues of network 2, E126 and R144 are essential for substrate binding . Residue M299 of network 1 and A273 of network 2 connect two sub-networks and are essential for substrate transport . The functional residues located on both the periplasmic and cytoplasmic sides suggest that the cooperative residues of both networks allow efficient allosteric communication for LacY operation by alternating between two major conformations, inward-facing and outward-facing conformation, respectively . The residues outside the main network, L84, Y350, and L351, lie close to the irreplaceable residue E126 (average Cα distance; 16.5Å) and mediate substrate translocation (Table 1).
Identification of cavity residues in other MFS transporters
The integration of evolutionary features worked well for the identification of functional residues of other family members of MFS transporters. We applied our method to the GlpT and EmrD proteins, the functional residues of which are less well characterized than those of LacY. We found that, similar to LacY, a few residues of GlpT and EmrD have high IS (Figure S3) and they use unique residue combinations for specific substrate binding and translocation. In GlpT, we chose 25 residues within the 90th percentile of IS. When we mapped the residues onto the GlpT structure, we found 18 of 25 residues located along the central cavity (Figure 5A and Table S4). Twenty-two of the detected residues form an interaction network (Figure 5B and Table S5), of which several residues have experimentally confirmed functional roles in substrate binding and translocation (Table S6). For example, residues K80, R269, and H165 have a critical role in substrate binding and residues E299, Y362, and Y393 participate in substrate translocation ,. In particular, the formation and breakage of salt bridges between residues H165, R269, and E299 are known to involve conformational changes during the transport of glycerol-3-phosphate . Meanwhile, in EmrD, 13 of 21 detected residues are located in the central cavity (Figure 5C and Table S7). Among them, 10 residues comprise the main interaction network associated with H+ translocation (Figure 5D and Tables S8, S9). It has been shown that residues Q21, Q24, T25, and I28 are involved in facilitating H+ translocation . Compared to LacY and GlpT, little is known about the functional mechanism of EmrD. Our analysis may serve as a guide for future experimental verification of EmrD functional residue location.
(A) ‘Open book’ view of detected residues in GlpT. Central cavity and non-cavity residue are shown in red and blue sticks, respectively. (B) Interaction network of the detected residues in GlpT. Of the 22 network comprising residues (left), 17 residues are found in central cavity (red sticks) and 5 residues are found in the non-cavity region (blue sticks). Dashed line indicates a van der Waals interaction. Bold line indicates a potential hydrogen bond or salt bridge. (C) Mapping high-IS residues onto the EmrD structure. (D) Interaction network of the detected residues of EmrD. Ten residues comprise a main interaction network (left).
Identification of cavity residues in other membrane protein transporters
To ensure that our method works for transporters outside of the MFS superfamily, we tested it on other membrane protein transporters, whose allosteric conformational changes were characterized and whose cavity residues could be selected from crystal structures –. We investigated the positions and annotated functional roles of high-IS residues in 15 membrane protein transporters, such as KvAP and Kv1.2 voltage-gated K+ channels, rhodopsin, the chloride pump halorhodopsin, bacteriorhodopsin, sensory rhodopsin, archaerhodopsin, Na+/K+ ATPase, P-type Ca2+ ATPase, plasma membrane ATPase, and the sulfate/molybdate ABC transporter. Membrane protein transporters mediate the movement of ions, solutes, and metabolites across a membrane . We found that, on average, IS selected 2.3 times more cavity residues than random selection (Table 2). Also, we discovered that many high-IS residues were located along the cavity region involved in substrate translocation pathways (Table S10) and comprised interaction networks in the protein structures (Figure S4). For example, in the chloride pump halorhodopsin, 10 of 15 residues were found from the chloride translocation pathway using the 90th percentile of IS (Figure 6A, shown in red spears)  and formed an interaction network. In sulfate/molydbate ABC transporter, 9 out of 12 detected residues were located in the substrate translocation pathway (Figure 6B, shown in red spears)  and 6 residues comprised an interaction network. In addition, 64% and 55% of the detected residues in the KvAP channel and P-type Ca2+ ATPase were located in the ion conduction pathway and formed an interaction network, respectively (Figures 6C and 6D) ,. These results showed IS to be an effective way to locate the cavity residues in the tested transporters. Also, in the precision-recall curves of four evolutionary approaches, IS had the highest precision at all levels of recall (Figure S5).
Positions of the detected residues are highlighted. Cavity residues are colored red and non-cavity residues are colored blue. The top view (left) and the side view (right) of membrane protein transporters are shown. (A) Chloride pump halorhodopsin (PDB ID: 1E12), (B) Sulfate/molybdate ABC transporter (PDB ID: 3D31), (C) KvAP voltage-gated K+ channel (PDB ID: 1ORQ), and (D) P-type Ca2+ ATPase (PDB ID: 1WPG).
In this study, we attempted to identify the functionally important cooperative residues of membrane protein transporters from amino acid sequences by integrating two different evolutionary features. We demonstrated that the conserved cores of evolutionarily coupled residues of MFS transporters were mainly located in the substrate translocation pathway. One may question why functionally important residues are conserved and have evolved in a co-dependent manner. It has been suggested that protein sequences may have been robust to environmental and mutational perturbations in the course of evolution in order to preserve protein function . These residues have evolved at a rate that was slow enough to avoid the loss of function . Indeed, we observed that central cavity residues of MFS transporters are moderately conserved and enriched between the 75th and 90th percentile of sequence conservation scores (Figure S1). This slow evolution rate allows correlative substitutions among functional residues, resulting in high co-evolutionary coupling numbers .
The presence of an interaction network of cooperative residues is strongly correlated with the pathway of substrate translocation described in other studies ,. We found that the cluster of cooperative residues comprised an interaction network that may constitute an allosteric pathway connecting the substrate binding site and translocation pathway of MFS transporters. Yifrach and colleagues found that allosteric pathway-lining residues are energetically coupled over long distances and showed that these residues are important for the sequential conformational transition of the Kv channel using electrophysiology recordings techniques ,. In addition, other researchers have shown that perturbations of conserved residues impair the allosteric communication of protein residues ,. These results suggest that cooperative residues are evolutionarily coupled and conserved to mediate long-range allosteric communication from the substrate binding site to the translocation pathway of membrane protein transporters.
The efficient regulation of allosteric communication is achieved through the interaction of cooperative residues. Recent network-based structural analyses by Nussinov and colleagues have shown that centrally positioned residues in protein structures maintain the robustness of allosteric pathways through residue-residue interactions , . By mapping the detected residues onto the ligand-free (PDB ID: 2CFQ) and ligand-bound (PDB ID: 1PV7) structures, we observed the rearrangement of residue-residue interactions. In particular, irreplaceable substrate binding residues, E126 and R144, had different interatomic contacts between ligand-free and ligand-bound structures (Figure S6). In the ligand-free structure, the guanidine group of R144 forms a salt bridge with the carboxyl group of E126; whereas, in the ligand-bound structure, the two atomic groups directly interact with the substrate by breaking the salt bridge ,. Also, the rearrangements of hydrogen bonds and salt bridges between residues Y236, D240, R302, K319, H322, and E325 are known to involve conformational changes in LacY . Taken together, we reasoned that the connectivity of the detected residues was changed because efficient conformational changes for substrate transport are regulated by the formation and breakage of interactions between cooperative residues.
We found that some of the high-IS residues in MFS transporters are non-cavity residues, while most of them are positioned in the central cavity to control substrate transport. It may be possible that some of the detected non-cavity residues are also involved in the transport mechanism. For example, it has been reported that a non-cavity residue, R302, of LacY is irreplaceable for substrate transport  and connected with central cavity residues, K319, Y236, D240, and H322 (Figure 4B and Table 1). Furthermore, we noticed that some non-cavity residues that have high-IS were found from the residue interaction networks of other membrane protein transporters (Figures S4). The detected non-cavity residues that surround the cavity region may have functional roles in membrane protein transporters.
Different MFS transporters may have diverse interaction networks of cooperative residues. We believe that the diversity of the networks occurs because evolution likely favors functional diversification of MFS transporters. Interestingly, we found that the interaction network of the detected residues in EmrD were found from only one symmetric half (where H+ translocation occurs); whereas, the networks of LacY and GlpT covered both symmetric halves. In EmrD, proton translocation and drug transport may occur at different sites in the central cavity . EmrD has a large and flexible substrate recognition pocket that transports various chemically unrelated drug compounds; therefore, different drugs may interact with different sites of the pocket . We suspect that the substrate recognition pocket of EmrD is not conserved so that functional residue detection is limited.
In summary, our integrative evolutionary analysis effectively shows that the conserved cores of evolutionarily coupled residues arose from functional constraints, providing information to characterize specific functional residues of MFS transporters. We believe this method can be applied to other proteins to narrow down the potential candidates of functional residues and to save time and reduce the cost incurred by molecular biology, biochemical, and biophysical approaches. We provide downloadable source code at our website (http://sbi.postech.ac.kr/IS/) for wide application of this method.
Materials and Methods
We obtained homologous sequences for LacY, GlpT, and EmrD of Escherichia coli and other membrane protein transporters from Swiss-Prot/TrEMBL. We used sequences 0.7∼1.4 times the query sequence length and <90% similarity to other sequences. We aligned the sequences using ClustalW . We omitted columns with a gap ≥20% and completely conserved region.
Quantification and integration of evolutionary information
To calculate the sequence conservation score of each residue in LacY, GlpT, EmrD, and other membrane protein transporters, we used ConSeq . We compared McBASC , SCA , and ELSC  algorithms for co-evolutionary analysis. The precision-recall curves showed a comparable performance in the identification of cavity residues among the different algorithms (Figure S7). Among them, the McBASC algorithm performed slightly better than other algorithms, so we used the McBASC algorithm to calculate co-evolution scores. We derived the co-evolutionary coupling number (CN) through the following steps. First, we selected significant co-evolving residue pairs using a length-dependent threshold . The number of co-evolving residue pairs is set equal to twice the protein length. Then, we counted the number of co-evolving residue pairs per residue and defined it as the CN. To correct the different score distributions, we normalized the sequence conservation score and CN by converting their scores into the corresponding percentile rank scores ranging from 0 to 1. Finally, we multiplied the normalized sequence conservation score by the CN to obtain the quantitative integration score (IS).
Selecting central cavity residues
We used a set of cavity residues (positive set) and a set of non-cavity residues (negative set) to evaluate the performances of IS, co-evolution, and sequence conservation scores. The central cavity residues of transporters are composed of the residues involved in substrate recognition, which are located in the pathway of substrate transport; whereas, non-cavity residues include the rest of the central cavity residues . To select central cavity residues, we measured the solvent accessible surface of translocation pathways of the three MFS transporter structures using VOIDOO with a 1.2 Å probe radius and default manner . We also manually inspected the selected residues to eliminate residues from other small cavities that can occur in the structure. In LacY, 49 of 417 residues, 53 of 452 residues in GlpT, and 52 of 394 residues in EmrD are in the central cavity and are tabulated in Table S2, S4, and S7, respectively.
Identification of functional residues and the construction of residue interaction networks
We investigated the functional implications of residues within the 90th percentile of IS. At the 90th percentile of IS, we can identify cavity residues with 5% false-positive rate, the fraction of non-cavity residues selected from the given percent cutoff. A 5% false-positive rate represents the acceptable level of selecting functionally important residues . Based on the observation that most of the detected residues were positioned in the transmembrane region (Figure S8), we considered the residues of the transmembrane region for further analysis where important functions of MFS transporters occur. We designated transmembrane boundaries for the three MFS transporters using the Protein Data Bank of Transmembrane Proteins (PDBTM) . We assessed the interatomic connectivity among the detected residues based on the crystal structures of MFS transporters in the Protein Data Bank (http://www.rcsb.org); PDB ID: 2CFQ for LacY, PDB ID: 1PW4 for GlpT, and PDB ID: 2GFP for EmrD. To measure interactions between residues, we used the contacts of structural units (CSU) software (http://www.weizmann.ac.il/sgedg/csu/). In a given protein structure, the CSU software provides a list of interatomic interactions and their distances by measuring the solvent-accessible surface of every atoms of two residues . A van der Waals interaction was identified if the distance between any two atoms of the residues is less than the sum of their van der Waals radii plus the diameter of a solvent molecule (2.8Å). A salt bridge was identified when the distance between the donor atoms (Nζ of Lys, Nζ, Nη1, Nη2 of Arg, Nδ1, Nε2 of His) and the acceptor atoms (Oε1, Oε2 of Glu, Oδ1, Oδ2 of Asp) was less than 4.0 Å . A hydrogen bond was assessed by HBPLUS , which measures the angle and distance of each donor-acceptor pair to find out its fitness to the geometric criteria defined by Baker and Hubbard .
Likelihood ratio calculation
We used likelihood ratios to statistically evaluate how well different evolutionary features (IS, CN, co-evolution, and sequence conservation scores) could discriminate central cavity residues from non-cavity residues for each of the following percentile groups: 80%, 82%, 84%, 86%, 88%, 90%, 92%, 94%, and 96%. We obtained likelihood ratios for different evolutionary features with:(1)X1 and X0 represent the number of central cavity and non-cavity residues selected from the given percent cutoff, respectively. H1 indicates the total number of central cavity residues. H0 is the total number of non-cavity residues. A likelihood ratio >1 indicates a reliable probability. An increasing likelihood ratio signifies the detection of more central cavity residues.
Data collection for extensive test to identify cavity residues
We tested our method on other membrane protein transporters. We collected the membrane protein transporters whose allosteric conformational changes were characterized and cavity residues can be selected from the crystal structures. We chose 15 protein structures from the five largest families of membrane protein transporters, which include KvAP and Kv1.2 voltage-gated K+ channels, rhodopsin, chloride pump halorhodopsin, bacteriorhodopsin, sensory rhodopsin, archaerhodopsin, Na+/K+ ATPase, P-type Ca2+ ATPase, plasma membrane ATPase, and sulfate/molybdate ABC transporter. Cavity residues were selected, as described in the procedure for selecting central cavity residues in MFS transporters.
Sliding window plots of sequence conservation-to-fraction of central cavity residues in LacY (A), GlpT (B), and EmrD (C).
(0.09 MB PDF)
Likelihood ratios of IS, CN, co-evolution, and sequence conservation scores.
(0.04 MB PDF)
IS pattern of GlpT and EmrD.
(0.06 MB PDF)
Interaction networks of the high-IS residues of membrane protein transporters.
(0.08 MB PDF)
Precision-recall curves of four evolutionary approaches.
(0.04 MB PDF)
Interaction networks of the detected residues of LacY.
(0.08 MB PDF)
Precision-recall curves of three algorithms for co-evolutionary analysis.
(0.03 MB PDF)
Positions of the detected functional residues are shown with the Z-coordinates of MFS transporters (A) LacY, (B) GlpT, and (C) EmrD.
(0.09 MB PDF)
Differences of IS, CN, and sequence conservation score between central cavity and non-cavity region.
(0.10 MB XLS)
List of central cavity residues in lactose permease (LacY).
(0.14 MB XLS)
Interaction network of detected residues in LacY.
(0.13 MB XLS)
List of central cavity residues in glycerol-3-phosphate transporter (GlpT).
(0.14 MB XLS)
Interaction network of detected residues in GlpT.
(0.13 MB XLS)
Functional implications and experimental evidence of the detected GlpT residues.
(0.11 MB XLS)
List of central cavity residues in multidrug transporter EmrD.
(0.13 MB XLS)
Interaction network of detected residues in EmrD.
(0.12 MB XLS)
Functional implications and experimental evidence of the detected EmrD residues.
(0.10 MB XLS)
We thank the SBI members, especially Seong-kyu Han for careful comments and programming.
Conceived and designed the experiments: JJ JSY SK. Performed the experiments: JJ. Analyzed the data: JJ JSY SK. Contributed reagents/materials/analysis tools: JJ JSY. Wrote the paper: JJ SK.
- 1. Sadovsky E, Yifrach O (2007) Principles underlying energetic coupling along an allosteric communication trajectory of a voltage-activated K+ channel. Proc Natl Acad Sci U S A 104: 19813–19818.E. SadovskyO. Yifrach2007Principles underlying energetic coupling along an allosteric communication trajectory of a voltage-activated K+ channel.Proc Natl Acad Sci U S A1041981319818
- 2. Pupko T, Bell RE, Mayrose I, Glaser F, Ben-Tal N (2002) Rate4Site: an algorithmic tool for the identification of functional regions in proteins by surface mapping of evolutionary determinants within their homologues. Bioinformatics 18: Suppl 1S71–77.T. PupkoRE BellI. MayroseF. GlaserN. Ben-Tal2002Rate4Site: an algorithmic tool for the identification of functional regions in proteins by surface mapping of evolutionary determinants within their homologues.Bioinformatics18Suppl 1S7177
- 3. Capra JA, Singh M (2007) Predicting functionally important residues from sequence conservation. Bioinformatics 23: 1875–1882.JA CapraM. Singh2007Predicting functionally important residues from sequence conservation.Bioinformatics2318751882
- 4. Liang S, Zhang C, Liu S, Zhou Y (2006) Protein binding site prediction using an empirical scoring function. Nucleic Acids Res 34: 3698–3707.S. LiangC. ZhangS. LiuY. Zhou2006Protein binding site prediction using an empirical scoring function.Nucleic Acids Res3436983707
- 5. Choi YS, Yang JS, Choi Y, Ryu SH, Kim S (2009) Evolutionary conservation in multiple faces of protein interaction. Proteins. YS ChoiJS YangY. ChoiSH RyuS. Kim2009Evolutionary conservation in multiple faces of protein interaction.Proteins
- 6. Gutteridge A, Bartlett GJ, Thornton JM (2003) Using a neural network and spatial clustering to predict the location of active sites in enzymes. J Mol Biol 330: 719–734.A. GutteridgeGJ BartlettJM Thornton2003Using a neural network and spatial clustering to predict the location of active sites in enzymes.J Mol Biol330719734
- 7. Hannenhalli SS, Russell RB (2000) Analysis and prediction of functional sub-types from protein sequence alignments. J Mol Biol 303: 61–76.SS HannenhalliRB Russell2000Analysis and prediction of functional sub-types from protein sequence alignments.J Mol Biol3036176
- 8. Yip KY, Patel P, Kim PM, Engelman DM, McDermott D, et al. (2008) An integrated system for studying residue coevolution in proteins. Bioinformatics 24: 290–292.KY YipP. PatelPM KimDM EngelmanD. McDermott2008An integrated system for studying residue coevolution in proteins.Bioinformatics24290292
- 9. Yeang CH, Haussler D (2007) Detecting coevolution in and among protein domains. PLoS Comput Biol 3: e211.CH YeangD. Haussler2007Detecting coevolution in and among protein domains.PLoS Comput Biol3e211
- 10. Goh CS, Bogan AA, Joachimiak M, Walther D, Cohen FE (2000) Co-evolution of proteins with their interaction partners. J Mol Biol 299: 283–293.CS GohAA BoganM. JoachimiakD. WaltherFE Cohen2000Co-evolution of proteins with their interaction partners.J Mol Biol299283293
- 11. Lockless SW, Ranganathan R (1999) Evolutionarily conserved pathways of energetic connectivity in protein families. Science 286: 295–299.SW LocklessR. Ranganathan1999Evolutionarily conserved pathways of energetic connectivity in protein families.Science286295299
- 12. Hatley ME, Lockless SW, Gibson SK, Gilman AG, Ranganathan R (2003) Allosteric determinants in guanine nucleotide-binding proteins. Proc Natl Acad Sci U S A 100: 14445–14450.ME HatleySW LocklessSK GibsonAG GilmanR. Ranganathan2003Allosteric determinants in guanine nucleotide-binding proteins.Proc Natl Acad Sci U S A1001444514450
- 13. Fodor AA, Aldrich RW (2004) On evolutionary conservation of thermodynamic coupling in proteins. J Biol Chem 279: 19046–19050.AA FodorRW Aldrich2004On evolutionary conservation of thermodynamic coupling in proteins.J Biol Chem2791904619050
- 14. Wang K, Samudrala R (2005) FSSA: a novel method for identifying functional signatures from structural alignments. Bioinformatics 21: 2969–2977.K. WangR. Samudrala2005FSSA: a novel method for identifying functional signatures from structural alignments.Bioinformatics2129692977
- 15. Poole AM, Ranganathan R (2006) Knowledge-based potentials in protein design. Curr Opin Struct Biol 16: 508–513.AM PooleR. Ranganathan2006Knowledge-based potentials in protein design.Curr Opin Struct Biol16508513
- 16. Goodey NM, Benkovic SJ (2008) Allosteric regulation and catalysis emerge via a common route. Nat Chem Biol 4: 474–482.NM GoodeySJ Benkovic2008Allosteric regulation and catalysis emerge via a common route.Nat Chem Biol4474482
- 17. Tang S, Liao JC, Dunn AR, Altman RB, Spudich JA, et al. (2007) Predicting allosteric communication in myosin via a pathway of conserved residues. J Mol Biol 373: 1361–1373.S. TangJC LiaoAR DunnRB AltmanJA Spudich2007Predicting allosteric communication in myosin via a pathway of conserved residues.J Mol Biol37313611373
- 18. Suel GM, Lockless SW, Wall MA, Ranganathan R (2003) Evolutionarily conserved networks of residues mediate allosteric communication in proteins. Nat Struct Biol 10: 59–69.GM SuelSW LocklessMA WallR. Ranganathan2003Evolutionarily conserved networks of residues mediate allosteric communication in proteins.Nat Struct Biol105969
- 19. Russ WP, Lowery DM, Mishra P, Yaffe MB, Ranganathan R (2005) Natural-like function in artificial WW domains. Nature 437: 579–583.WP RussDM LoweryP. MishraMB YaffeR. Ranganathan2005Natural-like function in artificial WW domains.Nature437579583
- 20. Pao SS, Paulsen IT, Saier MH, Jr (1998) Major facilitator superfamily. Microbiol Mol Biol Rev 62: 1–34.SS PaoIT PaulsenMH, Saier Jr1998Major facilitator superfamily.Microbiol Mol Biol Rev62134
- 21. Abramson J, Kaback HR, Iwata S (2004) Structural comparison of lactose permease and the glycerol-3-phosphate antiporter: members of the major facilitator superfamily. Curr Opin Struct Biol 14: 413–419.J. AbramsonHR KabackS. Iwata2004Structural comparison of lactose permease and the glycerol-3-phosphate antiporter: members of the major facilitator superfamily.Curr Opin Struct Biol14413419
- 22. Abramson J, Smirnova I, Kasho V, Verner G, Kaback HR, et al. (2003) Structure and mechanism of the lactose permease of Escherichia coli. Science 301: 610–615.J. AbramsonI. SmirnovaV. KashoG. VernerHR Kaback2003Structure and mechanism of the lactose permease of Escherichia coli.Science301610615
- 23. Huang Y, Lemieux MJ, Song J, Auer M, Wang DN (2003) Structure and mechanism of the glycerol-3-phosphate transporter from Escherichia coli. Science 301: 616–620.Y. HuangMJ LemieuxJ. SongM. AuerDN Wang2003Structure and mechanism of the glycerol-3-phosphate transporter from Escherichia coli.Science301616620
- 24. Yin Y, He X, Szewczyk P, Nguyen T, Chang G (2006) Structure of the multidrug transporter EmrD from Escherichia coli. Science 312: 741–744.Y. YinX. HeP. SzewczykT. NguyenG. Chang2006Structure of the multidrug transporter EmrD from Escherichia coli.Science312741744
- 25. Murakami S, Yamaguchi A (2003) Multidrug-exporting secondary transporters. Curr Opin Struct Biol 13: 443–452.S. MurakamiA. Yamaguchi2003Multidrug-exporting secondary transporters.Curr Opin Struct Biol13443452
- 26. Mintseris J, Weng Z (2005) Structure, function, and evolution of transient and obligate protein-protein interactions. Proc Natl Acad Sci U S A 102: 10930–10935.J. MintserisZ. Weng2005Structure, function, and evolution of transient and obligate protein-protein interactions.Proc Natl Acad Sci U S A1021093010935
- 27. Kaback HR, Sahin-Toth M, Weinglass AB (2001) The kamikaze approach to membrane transport. Nat Rev Mol Cell Biol 2: 610–620.HR KabackM. Sahin-TothAB Weinglass2001The kamikaze approach to membrane transport.Nat Rev Mol Cell Biol2610620
- 28. Frillingos S, Sahin-Toth M, Wu J, Kaback HR (1998) Cys-scanning mutagenesis: a novel approach to structure function relationships in polytopic membrane proteins. FASEB J 12: 1281–1299.S. FrillingosM. Sahin-TothJ. WuHR Kaback1998Cys-scanning mutagenesis: a novel approach to structure function relationships in polytopic membrane proteins.FASEB J1212811299
- 29. del Sol A, Fujihashi H, Amoros D, Nussinov R (2006) Residues crucial for maintaining short paths in network communication mediate signaling in proteins. Mol Syst Biol 2: 2006 0019.A. del SolH. FujihashiD. AmorosR. Nussinov2006Residues crucial for maintaining short paths in network communication mediate signaling in proteins.Mol Syst Biol22006 0019
- 30. Lee JI, Hwang PP, Hansen C, Wilson TH (1992) Possible salt bridges between transmembrane alpha-helices of the lactose carrier of Escherichia coli. J Biol Chem 267: 20758–20764.JI LeePP HwangC. HansenTH Wilson1992Possible salt bridges between transmembrane alpha-helices of the lactose carrier of Escherichia coli.J Biol Chem2672075820764
- 31. Abramson J, Iwata S, Kaback HR (2004) Lactose permease as a paradigm for membrane transport proteins (Review). Mol Membr Biol 21: 227–236.J. AbramsonS. IwataHR Kaback2004Lactose permease as a paradigm for membrane transport proteins (Review).Mol Membr Biol21227236
- 32. Guan L, Kaback HR (2006) Lessons from lactose permease. Annu Rev Biophys Biomol Struct 35: 67–91.L. GuanHR Kaback2006Lessons from lactose permease.Annu Rev Biophys Biomol Struct356791
- 33. Venkatesan P, Hu Y, Kaback HR (2000) Site-directed sulfhydryl labeling of the lactose permease of Escherichia coli: helix X. Biochemistry 39: 10656–10661.P. VenkatesanY. HuHR Kaback2000Site-directed sulfhydryl labeling of the lactose permease of Escherichia coli: helix X.Biochemistry391065610661
- 34. Frillingos S, Ujwal ML, Sun J, Kaback HR (1997) The role of helix VIII in the lactose permease of Escherichia coli: I. Cys-scanning mutagenesis. Protein Sci 6: 431–437.S. FrillingosML UjwalJ. SunHR Kaback1997The role of helix VIII in the lactose permease of Escherichia coli: I. Cys-scanning mutagenesis.Protein Sci6431437
- 35. Vadyvaloo V, Smirnova IN, Kasho VN, Kaback HR (2006) Conservation of residues involved in sugar/H(+) symport by the sucrose permease of Escherichia coli relative to lactose permease. J Mol Biol 358: 1051–1059.V. VadyvalooIN SmirnovaVN KashoHR Kaback2006Conservation of residues involved in sugar/H(+) symport by the sucrose permease of Escherichia coli relative to lactose permease.J Mol Biol35810511059
- 36. Naftalin RJ, Green N, Cunningham P (2007) Lactose permease H+-lactose symporter: mechanical switch or Brownian ratchet? Biophys J 92: 3474–3491.RJ NaftalinN. GreenP. Cunningham2007Lactose permease H+-lactose symporter: mechanical switch or Brownian ratchet?Biophys J9234743491
- 37. Wang Q, Voss J, Hubbell WL, Kaback HR (1998) Proximity of helices VIII (Ala273) and IX (Met299) in the lactose permease of Escherichia coli. Biochemistry 37: 4910–4915.Q. WangJ. VossWL HubbellHR Kaback1998Proximity of helices VIII (Ala273) and IX (Met299) in the lactose permease of Escherichia coli.Biochemistry3749104915
- 38. Lemieux MJ, Huang Y, Wang DN (2004) The structural basis of substrate translocation by the Escherichia coli glycerol-3-phosphate transporter: a member of the major facilitator superfamily. Curr Opin Struct Biol 14: 405–412.MJ LemieuxY. HuangDN Wang2004The structural basis of substrate translocation by the Escherichia coli glycerol-3-phosphate transporter: a member of the major facilitator superfamily.Curr Opin Struct Biol14405412
- 39. Law CJ, Maloney PC, Wang DN (2008) Ins and outs of major facilitator superfamily antiporters. Annu Rev Microbiol 62: 289–305.CJ LawPC MaloneyDN Wang2008Ins and outs of major facilitator superfamily antiporters.Annu Rev Microbiol62289305
- 40. Rees DC, Johnson E, Lewinson O (2009) ABC transporters: the power to change. Nat Rev Mol Cell Biol 10: 218–227.DC ReesE. JohnsonO. Lewinson2009ABC transporters: the power to change.Nat Rev Mol Cell Biol10218227
- 41. May LT, Leach K, Sexton PM, Christopoulos A (2007) Allosteric modulation of G protein-coupled receptors. Annu Rev Pharmacol Toxicol 47: 1–51.LT MayK. LeachPM SextonA. Christopoulos2007Allosteric modulation of G protein-coupled receptors.Annu Rev Pharmacol Toxicol47151
- 42. Fleishman SJ, Yifrach O, Ben-Tal N (2004) An evolutionarily conserved network of amino acids mediates gating in voltage-dependent potassium channels. J Mol Biol 340: 307–318.SJ FleishmanO. YifrachN. Ben-Tal2004An evolutionarily conserved network of amino acids mediates gating in voltage-dependent potassium channels.J Mol Biol340307318
- 43. Saier MH Jr, Tran CV, Barabote RD (2006) TCDB: the Transporter Classification Database for membrane transport protein analyses and information. Nucleic Acids Res 34: D181–186.MH Saier JrCV TranRD Barabote2006TCDB: the Transporter Classification Database for membrane transport protein analyses and information.Nucleic Acids Res34D181186
- 44. Kolbe M, Besir H, Essen LO, Oesterhelt D (2000) Structure of the light-driven chloride pump halorhodopsin at 1.8 A resolution. Science 288: 1390–1396.M. KolbeH. BesirLO EssenD. Oesterhelt2000Structure of the light-driven chloride pump halorhodopsin at 1.8 A resolution.Science28813901396
- 45. Gerber S, Comellas-Bigler M, Goetz BA, Locher KP (2008) Structural basis of trans-inhibition in a molybdate/tungstate ABC transporter. Science 321: 246–250.S. GerberM. Comellas-BiglerBA GoetzKP Locher2008Structural basis of trans-inhibition in a molybdate/tungstate ABC transporter.Science321246250
- 46. Jiang Y, Lee A, Chen J, Ruta V, Cadene M, et al. (2003) X-ray structure of a voltage-dependent K+ channel. Nature 423: 33–41.Y. JiangA. LeeJ. ChenV. RutaM. Cadene2003X-ray structure of a voltage-dependent K+ channel.Nature4233341
- 47. Toyoshima C, Nomura H, Tsuda T (2004) Lumenal gating mechanism revealed in calcium pump crystal structures with phosphate analogues. Nature 432: 361–368.C. ToyoshimaH. NomuraT. Tsuda2004Lumenal gating mechanism revealed in calcium pump crystal structures with phosphate analogues.Nature432361368
- 48. Devos DM, Pazos E., Valencia, A F. (2002) Multiple Sequence Alignments Information in Structure and Function Prediction: IOS Press publishers.83–94.DM DevosE. PazosF. Valencia, A2002Multiple Sequence Alignments Information in Structure and Function Prediction: IOS Press publishers.8394
- 49. Zuckerkandl EaP, L (1965) Evolutionary divergence and convergence in proteins. Evolving genes and proteins. New York: Evolving genes and proteins Academic Press. pp. 97–166.EaP, L. Zuckerkandl1965Evolutionary divergence and convergence in proteins.Evolving genes and proteinsNew YorkEvolving genes and proteins Academic Press97166
- 50. Law CJ, Almqvist J, Bernstein A, Goetz RM, Huang Y, et al. (2008) Salt-bridge dynamics control substrate-induced conformational change in the membrane transporter GlpT. J Mol Biol 378: 828–839.CJ LawJ. AlmqvistA. BernsteinRM GoetzY. Huang2008Salt-bridge dynamics control substrate-induced conformational change in the membrane transporter GlpT.J Mol Biol378828839
- 51. Zandany N, Ovadia M, Orr I, Yifrach O (2008) Direct analysis of cooperativity in multisubunit allosteric proteins. Proc Natl Acad Sci U S A 105: 11697–11702.N. ZandanyM. OvadiaI. OrrO. Yifrach2008Direct analysis of cooperativity in multisubunit allosteric proteins.Proc Natl Acad Sci U S A1051169711702
- 52. Aharoni A, Horovitz A (1996) Inter-ring communication is disrupted in the GroEL mutant Arg13→Gly; Ala126→Val with known crystal structure. J Mol Biol 258: 732–735.A. AharoniA. Horovitz1996Inter-ring communication is disrupted in the GroEL mutant Arg13→Gly; Ala126→Val with known crystal structure.J Mol Biol258732735
- 53. Horovitz A, Bochkareva ES, Girshovich AS (1993) The N terminus of the molecular chaperonin GroEL is a crucial structural element for its assembly. J Biol Chem 268: 9957–9959.A. HorovitzES BochkarevaAS Girshovich1993The N terminus of the molecular chaperonin GroEL is a crucial structural element for its assembly.J Biol Chem26899579959
- 54. Del Sol A, Arauzo-Bravo MJ, Amoros D, Nussinov R (2007) Modular architecture of protein structures and allosteric communications: potential implications for signaling proteins and regulatory linkages. Genome Biol 8: R92.A. Del SolMJ Arauzo-BravoD. AmorosR. Nussinov2007Modular architecture of protein structures and allosteric communications: potential implications for signaling proteins and regulatory linkages.Genome Biol8R92
- 55. Guan L, Sahin-Toth M, Kaback HR (2002) Changing the lactose permease of Escherichia coli into a galactose-specific symporter. Proc Natl Acad Sci U S A 99: 6613–6618.L. GuanM. Sahin-TothHR Kaback2002Changing the lactose permease of Escherichia coli into a galactose-specific symporter.Proc Natl Acad Sci U S A9966136618
- 56. Mirza O, Guan L, Verner G, Iwata S, Kaback HR (2006) Structural evidence for induced fit and a mechanism for sugar/H+ symport in LacY. EMBO J 25: 1177–1183.O. MirzaL. GuanG. VernerS. IwataHR Kaback2006Structural evidence for induced fit and a mechanism for sugar/H+ symport in LacY.EMBO J2511771183
- 57. Lewinson O, Adler J, Sigal N, Bibi E (2006) Promiscuity in multidrug recognition and transport: the bacterial MFS Mdr transporters. Mol Microbiol 61: 277–284.O. LewinsonJ. AdlerN. SigalE. Bibi2006Promiscuity in multidrug recognition and transport: the bacterial MFS Mdr transporters.Mol Microbiol61277284
- 58. Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22: 4673–4680.JD ThompsonDG HigginsTJ Gibson1994CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.Nucleic Acids Res2246734680
- 59. Berezin C, Glaser F, Rosenberg J, Paz I, Pupko T, et al. (2004) ConSeq: the identification of functionally and structurally important residues in protein sequences. Bioinformatics 20: 1322–1324.C. BerezinF. GlaserJ. RosenbergI. PazT. Pupko2004ConSeq: the identification of functionally and structurally important residues in protein sequences.Bioinformatics2013221324
- 60. Olmea O, Rost B, Valencia A (1999) Effective use of sequence correlation and conservation in fold recognition. J Mol Biol 293: 1221–1239.O. OlmeaB. RostA. Valencia1999Effective use of sequence correlation and conservation in fold recognition.J Mol Biol29312211239
- 61. Dekker JP, Fodor A, Aldrich RW, Yellen G (2004) A perturbation-based method for calculating explicit likelihood of evolutionary co-variance in multiple sequence alignments. Bioinformatics 20: 1565–1572.JP DekkerA. FodorRW AldrichG. Yellen2004A perturbation-based method for calculating explicit likelihood of evolutionary co-variance in multiple sequence alignments.Bioinformatics2015651572
- 62. Fuchs A, Martin-Galiano AJ, Kalman M, Fleishman S, Ben-Tal N, et al. (2007) Co-evolving residues in membrane proteins. Bioinformatics 23: 3312–3319.A. FuchsAJ Martin-GalianoM. KalmanS. FleishmanN. Ben-Tal2007Co-evolving residues in membrane proteins.Bioinformatics2333123319
- 63. Kleywegt GJ, Jones TA (1994) Detection, delineation, measurement and display of cavities in macromolecular structures. Acta Crystallogr D Biol Crystallogr 50: 178–185.GJ KleywegtTA Jones1994Detection, delineation, measurement and display of cavities in macromolecular structures.Acta Crystallogr D Biol Crystallogr50178185
- 64. Thornton KR, Jensen JD (2007) Controlling the false-positive rate in multilocus genome scans for selection. Genetics 175: 737–750.KR ThorntonJD Jensen2007Controlling the false-positive rate in multilocus genome scans for selection.Genetics175737750
- 65. Tusnady GE, Dosztanyi Z, Simon I (2005) PDB_TM: selection and membrane localization of transmembrane proteins in the protein data bank. Nucleic Acids Res 33: D275–278.GE TusnadyZ. DosztanyiI. Simon2005PDB_TM: selection and membrane localization of transmembrane proteins in the protein data bank.Nucleic Acids Res33D275278
- 66. Sobolev V, Sorokine A, Prilusky J, Abola EE, Edelman M (1999) Automated analysis of interatomic contacts in proteins. Bioinformatics 15: 327–332.V. SobolevA. SorokineJ. PriluskyEE AbolaM. Edelman1999Automated analysis of interatomic contacts in proteins.Bioinformatics15327332
- 67. Xu D, Tsai CJ, Nussinov R (1997) Hydrogen bonds and salt bridges across protein-protein interfaces. Protein Eng 10: 999–1012.D. XuCJ TsaiR. Nussinov1997Hydrogen bonds and salt bridges across protein-protein interfaces.Protein Eng109991012
- 68. McDonald IK, Thornton JM (1994) Satisfying hydrogen bonding potential in proteins. J Mol Biol 238: 777–793.IK McDonaldJM Thornton1994Satisfying hydrogen bonding potential in proteins.J Mol Biol238777793
- 69. Baker EN, Hubbard RE (1984) Hydrogen bonding in globular proteins. Prog Biophys Mol Biol 44: 97–179.EN BakerRE Hubbard1984Hydrogen bonding in globular proteins.Prog Biophys Mol Biol4497179
- 70. Sahin-Toth M, Frillingos S, Bibi E, Gonzalez A, Kaback HR (1994) The role of transmembrane domain III in the lactose permease of Escherichia coli. Protein Sci 3: 2302–2310.M. Sahin-TothS. FrillingosE. BibiA. GonzalezHR Kaback1994The role of transmembrane domain III in the lactose permease of Escherichia coli.Protein Sci323022310
- 71. Ermolova N, Madhvani RV, Kaback HR (2006) Site-directed alkylation of cysteine replacements in the lactose permease of Escherichia coli: helices I, III, VI, and XI. Biochemistry 45: 4182–4189.N. ErmolovaRV MadhvaniHR Kaback2006Site-directed alkylation of cysteine replacements in the lactose permease of Escherichia coli: helices I, III, VI, and XI.Biochemistry4541824189
- 72. Venkatesan P, Kwaw I, Hu Y, Kaback HR (2000) Site-directed sulfhydryl labeling of the lactose permease of Escherichia coli: helix VII. Biochemistry 39: 10641–10648.P. VenkatesanI. KwawY. HuHR Kaback2000Site-directed sulfhydryl labeling of the lactose permease of Escherichia coli: helix VII.Biochemistry391064110648
- 73. Roepe PD, Zbar RI, Sarkar HK, Kaback HR (1989) A five-residue sequence near the carboxyl terminus of the polytopic membrane protein lac permease is required for stability within the membrane. Proc Natl Acad Sci U S A 86: 3992–3996.PD RoepeRI ZbarHK SarkarHR Kaback1989A five-residue sequence near the carboxyl terminus of the polytopic membrane protein lac permease is required for stability within the membrane.Proc Natl Acad Sci U S A8639923996