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Intricate Knots in Proteins: Function and Evolution

  • Peter Virnau ,

    To whom correspondence should be addressed. E-mail: virnau@mit.edu

    Affiliation Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America

  • Leonid A Mirny,

    Affiliations Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America , Harvard–MIT Division of Health Sciences and Technology, Cambridge, Massachusetts, United States of America

  • Mehran Kardar

    Affiliation Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America

Intricate Knots in Proteins: Function and Evolution

  • Peter Virnau, 
  • Leonid A Mirny, 
  • Mehran Kardar
PLOS
x

Abstract

Our investigation of knotted structures in the Protein Data Bank reveals the most complicated knot discovered to date. We suggest that the occurrence of this knot in a human ubiquitin hydrolase might be related to the role of the enzyme in protein degradation. While knots are usually preserved among homologues, we also identify an exception in a transcarbamylase. This allows us to exemplify the function of knots in proteins and to suggest how they may have been created.

Synopsis

Several protein structures incorporate a rather unusual structural feature: a knot in the polypeptide backbone. These knots are extremely rare, but their occurrence is likely connected to protein function in as yet unexplored fashion. The authors' analysis of the complete Protein Data Bank reveals several new knots that, along with previously discovered ones, may shed light on such connections. In particular, they identify the most complex knot discovered to date in a human protein, and suggest that its entangled topology protects it against unfolding and degradation. Knots in proteins are typically preserved across species and sometimes even across kingdoms. However, there is also one example of a knot in a protein that is not present in a closely related structure. The emergence of this particular knot is accompanied by a shift in the enzymatic function of the protein. It is suggested that the simple insertion of a short DNA fragment into the gene may suffice to cause this alteration of structure and function.

Introduction

Although knots are abundant and complex in globular homopolymers [13], they are rare and simple in proteins [48]. Sixteen methyltransferases in bacteria and viruses can be combined into the α/β knot superfamily [9], and several isozymes of carbonic anhydrase (I, II, IV, V) are known to be knotted. Apart from these two folds, only a few insular knots have been reported [5,6,10,11], some of which were derived from incomplete structures [6,11]. For the most part, knotted proteins contain simple trefoil knots (31) that can be represented by three essential crossings in a projection onto a plane (see Figure 1, left). Only three proteins were identified with four projected crossings (41, Figure 1, middle).

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Figure 1. Examples of the Three Different Types of Knots Found in Proteins

Colors change continuously from red (first residue) to blue (last residue). A reduced representation of the structure, based on the algorithm described in [1,6,36], is shown in the lower row.

(Left) The trefoil knot (31) in the YBEA methyltransferase from E. coli (pdb code 1ns5; unpublished data) reveals three essential crossings in a projection onto a plane.

(Middle) The figure-eight knot (41) in the Class II ketol-acid reductoisomerase from Spinacia oleracea (pdb code 1yve [26]) features four crossings. (Only the knotted section of the protein is shown.)

(Right) The knot 52 in ubiquitin hydrolase UCH-L3 (pdb code 1xd3 [18]) reveals five crossings. Pictures were generated with Visual Molecular Dynamics (http://www.ks.uiuc.edu/Research/vmd) [43].

https://doi.org/10.1371/journal.pcbi.0020122.g001

In this report we provide the first comprehensive review of knots in proteins, which considers all entries in the Protein Data Bank (http://www.pdb.org) [12], and not just a subset. This allows us to examine knots in homologous proteins. Our analysis reveals several new knots, all in enzymes. In particular, we discovered the most complicated knot found to date (52) in human ubiquitin hydrolase (Figure 1, right), and suggest that its entangled topology protects it against being pulled into the proteasome. We also noticed that knots are usually preserved among structural homologues. Sequence similarity appears to be a strong indicator for the preservation of topology, although differences between knotted and unknotted structures are sometimes subtle. Interestingly, we have also identified a novel knot in a transcarbamylase that is not present in homologues of known structure. We show that the presence of this knot alters the functionality of the protein, and suggest how the knot may have been created in the first place.

Mathematically, knots are rigorously defined in closed loops [13]. Fortunately, both the N- and C-termini of open proteins are typically accessible from the surface and can be connected unambiguously: we reduce the protein to its Cα- backbone, and draw two lines outward starting at the termini in the direction of the connection line between the center of mass of the backbone and the respective ends [5]. The lines are joined by a big loop, and the structure is topologically classified by the determination of its Alexander polynomial [1,13]. Applying this method to the Protein Data Bank in the version of January 3, 2006, we found 273 knotted structures in the 32,853 entries that contain proteins (Table S1). Knots formed by disulfide [14,15] or hydrogen bonds [7] were not included in the study.

Results

For further analysis, we considered 36 proteins that contain knots as defined by rather stringent criteria discussed in the Materials and Methods section. These proteins can be classified into six distinct families (Table 1). Four of these families incorporate a deeply knotted section, which persists when 25 amino acids are cut off from either terminus. Interestingly, all knotted proteins thus identified are enzymes. Our investigation affirms that all members of the carbonic anhydrase fold (including the previously undetermined isozymes III, VII, and XIV) are knotted. In addition, we identify a novel trefoil in two bacterial transcarbamylase-like proteins (AOTCase in Xanthomonas campestris and SOTCase in Bacteroides fragilis) [16,17].

UCH-L3—The most complex protein knot.

One of our most intriguing discoveries is a fairly intricate knot with five projected crossings (52) in ubiquitin hydrolase (UCH-L3 [18]; see Figure 1, right). This knot is the first of its kind and, apart from carbonic anhydrases, the only identified in a human protein. Human UCH-L3 also has a yeast homologue [6,19] with a sequence identity of 32% [20]. Amino acids 63 to 77 are unstructured, and if we connect the unstructured region by an arc that is present in the human structure, we obtain the same knot with five crossings. What may be the function of this knot? In eukaryotes, proteins get labeled for degradation by ubiquitin conjugation. UCH-L3 performs deconjugation of ubiquitin, thus rescuing proteins from degradation. The close association of the enzyme with ubiquitin should make it a prime target for degradation at the proteasome. We suggest that the knotted structure of UCH-L3 makes it resistant to degradation. In fact, the first step of protein degradation was shown to be ATP-dependent protein unfolding by threading through a narrow pore (~13 Å in diameter) of a proteasome [21,22]. Such threading into the degradation chamber depends on how easily a protein unfolds, with more stable proteins being released back into solution [23] and unstable ones being degraded. If ATP-dependent unfolding proceeds by pulling the C-terminus into a narrow pore [21], then a knot can sterically preclude such translocation, hence preventing protein unfolding and degradation. While arceabacterial proteasome PAN was shown to process proteins from its C- to N-terminus [21], it cannot be ruled out that some eukaryotic proteasomes process proteins in the N- to C-direction, thus requiring protection of both termini. Unfolding of a knotted protein by pulling may require a long time for global unfolding and untangling of the knot. Unknotted proteins, in contrast, have been shown to become unstable if a few residues are removed from their termini [24], suggesting that threading a few (5–10) residues into a proteasomal pore would be sufficient to unravel an unknotted structure. At both termini, UCH-L3 contains loops entangled into the knot protecting both ends against unfolding if pulled. It should also be noted that both N- and C-termini are stabilized by a number of hydrophobic interactions with the rest of the protein. The C-terminus is particularly stable—residues 223 to 229 are hydrophobic and form numerous contacts at 5 Å with the rest of the structure.

We would like to stress that this hypothesis needs to be tested by experiments. Different proteins may also provide different levels of protection against degradation, depending on structural details, the depth of the knot, and its complexity. Recently, a knot in the red/far-red light photoreceptor phytochrome A in Deinococcus radiodurans was identified [11] (see Materials and Methods). Although sequence similarity suggests that the knot may also be present in plant homologues, we cannot be certain. In plants, the red-absorbing form is rather stable (half-life of 1 wk), but the far-red–absorbing form is degraded upon photoconversion by the proteasome with a half-life of 1–2 h in seedlings (and somewhat longer in adult plants) [25].

Evolutionary aspects.

As expected, homologous structures tend to retain topological features. The trefoil knot in carbonic anhydrase can be found in isozymes ranging from bacteria and algae to humans (Table 1). Class II ketol-acid reductoisomerase comprises a figure-eight knot present in Escherichia coli [10] and spinach [26] (see Figure 1, middle), and S-adenosylmethione synthetase contains a deep trefoil knot in E. coli [5,27] and rat [28]. It appears that particular knots have indeed been preserved throughout evolution, which suggests a crucial role for knots in protein enzymatic activity and binding.

UCH-L3 in human and yeast share only 33% [29] of their sequences, but contain the same 5-fold knot as far as we can tell from the incomplete structure in yeast. It is not only likely that all species in between have the same knot—the link between sequence and structure may also be used to predict candidates for knots among isozymes or related proteins for which the structure is unknown. For example, UCH-L4 in mouse has 96% sequence identity with human UCH-L3. The similarity with UCH-L6 in chicken is 86%, and with UCH-L1 about 55%. Indeed, a reexamination of the most recent Protein Data Bank entries revealed that UCH-L1 contains the same 52 knot as UCH-L3. (See the Update section—the structure was not yet part of the January Protein Data Bank release on which this paper is based.) Unfortunately, the method is not foolproof because differences between knotted and unknotted structures are sometime subtle. As we will demonstrate in the next paragraph, a more reliable estimate has to consider the conservation of major elements of the knot, like loops and threads.

AOTCase—How a protein knot can alter enzymatic activity.

Somewhat surprisingly, we also identified a pair of homologues for which topology is not preserved. N-acetylornithine transcarbamylase (AOTCase [17]) is essential for the arginine biosynthesis in several major pathogens. In other bacteria, animals, and humans, a homologous enzyme (OTCase) processes L-ornithine instead [30]. Both proteins have two active sites. The first one binds carbamyl phosphate to the enzyme. The second site binds acetylornithine in AOTCases and L-ornithine in OTCases, enabling a reaction with carbamyl phosphate to form acetylcitrulline or citrulline, respectively [17, 31].

AOTCase in X. campestris has 41% sequence identity with OTCase from Pyrococcus furiosus [32] and 29% with human OTCase [31]. As demonstrated in Figure 2, AOTCase contains a deep trefoil knot which is not present in OTCase (Figure 2, right) and which modifies the second active site. The knot consists of a rigid proline-rich loop (residues 178–185), through which residues 252 to 256 are threaded and affixed. As elaborated in [17], the reaction product N-acetylcitrulline strongly interacts with the loop and with Lys252. Access to subsequent residues is, however, restricted by the knot. L-norvaline in Figure 2 (right) is very similar to L-ornithine but lacks the N-ɛ atom of the latter to prevent a reaction with carbamyl phosphate. As the knot is not present in OTCase, the ligand has complete access to the dangling residues 263–268 and strongly interacts with them [31]. This leads to a rotation of the carboxyl-group by roughly 110° around the Cα–Cβ bond [17].

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Figure 2. Structures of Transcarbamylase from X. campestris with a Trefoil Knot and from Human without a Knot

(Left) Knotted section (residues 171–278) of N-acetylornithine transcarbamylase from X. campestris with reaction product N-acetylcitrulline (pdb code 1yh1 [17]) and interacting side chains.

(Right) Corresponding (unknotted) section (residues 189–286) in human ornithine transcarbamylase (pdb code 1c9y [31]) with inhibitor L-norvaline and carbamyl phosphate. Colors change continuously from red (first residue in the section) to blue (last residue in the section). The two proteins have an overall sequence identity of 29% [41]. Pictures were generated with VMD [43].

https://doi.org/10.1371/journal.pcbi.0020122.g002

This example demonstrates how the presence of a knot can modify active sites and alter the enzymatic activity of a protein—in this case, from processing L-ornithine to N-acetyl-L-ornithine. It is also easy to imagine how this alteration happened: a short insertion extends the loop and modifies the folding pathway of the protein.

Discussion

Nature appears to disfavour entanglements, and evolution has developed mechanisms to avoid knots. Human DNA wraps around histone proteins, and the rigidity of DNA allows it to form a spool when it is fed into a viral capsid. One end also stays in the loading channel and prevents subsequent equilibration [33]. Knotted proteins are rare, although the reason is far less well understood. Can the absence of entanglement be explained in terms of particular statistical ensembles, or is there an evolutionary bias? And how do these structures actually fold?

Knots are ubiquitous in globular homopolymers [13,8], but rare in coil-like phases [1,3436]. It is likely that even a flexible polymer will at least initially remain unknotted after a collapse from a swollen state. In proteins, the free energy landscape is considerably more complex, which may allow most proteins to stay unknotted. The secondary structure and the stiffness of the protein backbone may shift the length scale at which knots typically appear, too [8]. If knotted proteins are in fact more difficult to degrade, it might also be disadvantageous for most proteins to be knotted in the first place.

Unfortunately, few experimental papers address folding and biophysical aspects of knots in proteins. In recent work [37], Jackson and Mallam reversibly unfolded and folded a knotted methyltransferase in vitro, indicating that chaperones are not a necessary prerequisite. In a subsequent study [38], the authors provide an extensive kinetic analysis of the folding pathway. In conclusion, we would like to express our hope that this report will inspire more experiments in this small but nevertheless fascinating field.

Materials and Methods

To determine whether a structure is knotted, we reduce the protein to its backbone, and draw two lines outward starting at the termini in the direction of the connection line between the center of mass of the backbone and the respective ends. These two lines are joined by a big loop, and the structure is classified by the determination of its Alexander polynomial [1,13]. To determine the size of the knotted core, we delete successively amino acids from the N-terminus until the protein becomes unknotted [1,6]. The procedure is repeated at the C-terminus starting with the last structure that contained the original knot. For each deletion, the outward pointing line through the new termini is parallel to the respective lines computed for the full structure. The thus determined size should, however, only be regarded as a guideline. A better estimate can be achieved by looking at the structure.

In Table 1 we include knotted structures with no missing amino acids in the center of the protein. (A list of potentially knotted structures with missing amino acids can be found in Table S3.) Technically, the numbering of the residues in the mmcif file has to be subsequent, and no two amino acids are allowed to be more than 6 Å apart. In addition, the knot has to persist when two amino acids are cut from either terminus. We have further excluded structures for which unknotted counterexamples exist (e.g., only one nuclear magnetic resonance structure among many is knotted or another structure of the same protein is unknotted). If a structure is fragmented, the knot has to appear in one fragment and in the resulting structure obtained from connecting missing sections by straight lines. Other knotted structures are only considered when at least one additional member of the same structural family [9] contains a knot according to the criteria above.

The enforcement of these rules leads to the exclusion of the bluetongue virus core protein [6] (41) and photoreceptor phytochrome A in D. radiodurans [11] (31), which have been previously identified as being knotted. Both structures are fragmented and become knotted only when a few missing fragments are connected by straight lines. In the viral core protein, the dangling C-terminus threads through a loose loop and becomes knotted in one out of two cases. On the other hand, the photoreceptor phytochrome A appears to contain a true knot. Notably, our analysis suggests that the thus connected structure of phytochrome A contains a figure-eight knot instead of a trefoil as reported in [11]. Moreover, we excluded a structure of the Autographa California nuclear polyhedrosis virus, which contains a knot according to our criteria. However, the N-terminus is buried inside the protein and the knot only exists because of our specific connection to the outside.

To further validate our criteria, we implemented an alternative method [4,8,39] that relies on the statistical analysis of multiple random closures. We arbitrarily chose two points on a sphere (which has to be larger than the protein) and connected each with one terminus. The two points can be joined unambiguously, and the resulting loop was analyzed by calculating the Alexander polynomial. We repeated the procedure 1,000 times, and defined the knot as the majority type.

Applying this analysis, we discovered 241 knotted structures in the Protein Data Bank. All 241 structures are also present in the 273 structures (Table S1) that were identified by our method, and the knot type is the same. The missing 32 structures (Table S2) are mostly shallow knots and were already rejected according to our extended criteria. The random closure also correctly discards rare structures with buried termini. In conclusion, the method used in this paper is considerably faster but requires a slightly increased inspection effort. Our observations agree with [8], which provides an extensive comparison of closures applied to proteins. A complete listing of knotted Protein Data Bank structures is given in the Supporting Information.

Update.

Recently, the structure of human UCH-L1 was solved and released [40]. The protein shares 55% sequence identity with UCH-L3 [41], and it contains the same 5-fold knot. UCH-L1 is highly abundant in the brain, comprising up to 2% of the total brain protein [42]. The structure of UCH-L1 was not yet part of the January Protein Data Bank edition on which the rest of this study is based. We also noticed several new structures of knotted transcarbamylase-like proteins.

Supporting Information

Table S1. List of Knotted Protein Data Bank Entries

https://doi.org/10.1371/journal.pcbi.0020122.st001

(79 KB DOC)

Table S2. List of Knotted Entries from Table S1 That Become Unknotted When Ends Are Connected by the Random Closure Method

https://doi.org/10.1371/journal.pcbi.0020122.st002

(28 KB DOC)

Table S3. List of Structures That Become Knotted When Missing Sections Are Joined by Straight Lines

https://doi.org/10.1371/journal.pcbi.0020122.st003

(35 KB DOC)

Accession Numbers

The Protein Data Bank (http://www.pdb.org) accession numbers for the structures discussed in this paper are human UCH-L3 (1xd3), UCH-L3 yeast homologue (1cmx), human UCH-L1 (2etl), photoreceptor phytochrome A in D. radiodurans (1ztu), class II ketol-acid reductoisomerase in E. coli (1yrl), class II ketol-acid reductoisomerase in spinach (1yve), S-adenosylmethione synthetase in E. coli (1fug), S-adenosylmethione synthetase in rat (1qm4), AOTCase from X. campestris (1yh1), SOTCase from B. fragilis (1js1), OTCase from P. furiosus (1a1s), OTCase from human (1c9y), bluetongue virus core protein (2btv), and baculovirus P35 protein in Autographa California nuclear polyhedrosis virus (1p35).

Acknowledgments

Upon completion of this work we became aware of a related study [8], which independently identified the knots in UCH-L3 and SOTCase in a re-examination of protein knots. PV would like to acknowledge discussions with François Nédélec and with Olav Zimmermann, in which they proposed the potential link between protein knots and degradation. LM and PV would also like to thank Rachel Gaudet for a discussion about the function of ubiquitin hydrolase.

Author Contributions

MK conceived the study. PV designed and wrote the analysis code. PV and LM analyzed the data. PV, LM, and MK wrote the paper.

References

  1. 1. Virnau P, Kantor Y, Kardar M (2005) Knots in globule and coil phases of a model polyethylene. J Am Chem Soc 127: 15102–15106.P. VirnauY. KantorM. Kardar2005Knots in globule and coil phases of a model polyethylene.J Am Chem Soc1271510215106
  2. 2. Mansfield ML (1994) Knots in Hamilton cycles. Macromolecules 27: 5924–5926.ML Mansfield1994Knots in Hamilton cycles.Macromolecules2759245926
  3. 3. Lua RC, Borovinskiy AL, Grosberg AY (2004) Fractal and statistical properties of large compact polymers: A computational study. Polymer 45: 717–731.RC LuaAL BorovinskiyAY Grosberg2004Fractal and statistical properties of large compact polymers: A computational study.Polymer45717731
  4. 4. Mansfield ML (1994) Are there knots in proteins? Nat Struct Mol Bio 1: 213–214.ML Mansfield1994Are there knots in proteins?Nat Struct Mol Bio1213214
  5. 5. Mansfield ML (1997) Fit to be tied. Nat Struct Mol Bio 4: 166–167.ML Mansfield1997Fit to be tied.Nat Struct Mol Bio4166167
  6. 6. Taylor WR (2000) A deeply knotted protein structure and how it might fold. Nature 406: 916–919.WR Taylor2000A deeply knotted protein structure and how it might fold.Nature406916919
  7. 7. Taylor WR, Lin K (2003) Protein knots—A tangled problem. Nature 421: 25.WR TaylorK. Lin2003Protein knots—A tangled problem.Nature42125
  8. 8. Lua RC, Grosberg AY (2006) Statistics of knots, geometry of conformations, and evolution of proteins. PLOS Comp Biol 2: e45.RC LuaAY Grosberg2006Statistics of knots, geometry of conformations, and evolution of proteins.PLOS Comp Biol2e45
  9. 9. Murzin AG, Brenner SE, Hubbard T, Chothia C (1995) SCOP: A structural classification of proteins database for the investigation of sequences and structures. J Mol Biol 247: 536–540.AG MurzinSE BrennerT. HubbardC. Chothia1995SCOP: A structural classification of proteins database for the investigation of sequences and structures.J Mol Biol247536540http://scop.mrc-lmb.cam.ac.uk/scop. http://scop.mrc-lmb.cam.ac.uk/scop.
  10. 10. Tyagi R, Duquerroy S, Navaza J, Guddat LW, Duggleby RG (2005) The crystal structure of a bacterial Class II ketol-acid reductolsomerase: Domain conservation and evolution. Protein Sci 14: 3089–3100.R. TyagiS. DuquerroyJ. NavazaLW GuddatRG Duggleby2005The crystal structure of a bacterial Class II ketol-acid reductolsomerase: Domain conservation and evolution.Protein Sci1430893100
  11. 11. Wagner JR, Brunzelle JS, Forest KT, Vierstra RD (2005) A light-sensing knot revealed by the structure of the chromophore-binding domain of phytochrome. Nature 438: 325–331.JR WagnerJS BrunzelleKT ForestRD Vierstra2005A light-sensing knot revealed by the structure of the chromophore-binding domain of phytochrome.Nature438325331
  12. 12. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, et al. (2000) The Protein Data Bank. Nucleic Acids Res 28: 235–242.HM BermanJ. WestbrookZ. FengG. GillilandTN Bhat2000The Protein Data Bank.Nucleic Acids Res28235242(The Protein Data Bank is athttp://www.pdb.org. Accessed 22 August 2006.). (The Protein Data Bank is athttp://www.pdb.org. Accessed 22 August 2006.).
  13. 13. CC Adams 1994 The knot book: An elementary introduction to the mathematical theory of knots New York W. H. Freeman. 306 p.
  14. 14. Liang C, Mislow K (1995) Topological features of protein structures: Knots and links. J Am Chem Soc 177: 4201–4213.C. LiangK. Mislow1995Topological features of protein structures: Knots and links.J Am Chem Soc17742014213
  15. 15. Takusagawa F, Kamitori S (1996) A real knot in protein. J Am Chem Soc 118: 8945–8946.F. TakusagawaS. Kamitori1996A real knot in protein.J Am Chem Soc11889458946
  16. 16. Shi D, Gallegos R, DePonte J III, Morizono H, Yu X, et al. (2002) Crystal structure of a transcarbamylase-like protein from the anaerobic bacterium Bacteroides fragilis at 2.0 A resolution. J Mol Biol 320: 899–908.D. ShiR. GallegosJ. DePonte IIIH. MorizonoX. Yu2002Crystal structure of a transcarbamylase-like protein from the anaerobic bacterium Bacteroides fragilis at 2.0 A resolution.J Mol Biol320899908
  17. 17. Shi D, Morizono H, Yu X, Roth L, Caldovic L, et al. (2005) Crystal structure of N-acetylornithine transcarbamylase from Xanthomonas campestris: A novel enzyme in a new arginine biosynthetic pathway found in several eubacteria. J Biol Chem 280: 14366–14369.D. ShiH. MorizonoX. YuL. RothL. Caldovic2005Crystal structure of N-acetylornithine transcarbamylase from Xanthomonas campestris: A novel enzyme in a new arginine biosynthetic pathway found in several eubacteria.J Biol Chem2801436614369
  18. 18. Misaghi S, Galardy PJ, Meester WJN, Ovaa H, Ploegh HL, et al. (2005) Structure of the ubiquitin hydrolase Uch-L3 complexed with a suicide substrate. J Biol Chem 280: 1512–1520.S. MisaghiPJ GalardyWJN MeesterH. OvaaHL Ploegh2005Structure of the ubiquitin hydrolase Uch-L3 complexed with a suicide substrate.J Biol Chem28015121520
  19. 19. Johnston SC, Riddle SM, Cohen RE, Hill CP (1999) Structural basis for the specificity of ubiquitin C-terminal hydrolases. EMBO J 18: 3877–3887.SC JohnstonSM RiddleRE CohenCP Hill1999Structural basis for the specificity of ubiquitin C-terminal hydrolases.EMBO J1838773887
  20. 20. Holm L, Sander C (1996) Mapping the protein universe. Science 273: 595–602.L. HolmC. Sander1996Mapping the protein universe.Science273595602(The Dali Database is located at http://ekhidna.biocenter.helsinki.fi/dali/start. Accessed 22 August 2006.). (The Dali Database is located at http://ekhidna.biocenter.helsinki.fi/dali/start. Accessed 22 August 2006.).
  21. 21. Navon A, Goldberg AL (2001) Proteins are unfolded on the surface of the ATPase ring before transport into the proteasome. Mol Cell 8: 1339–1349.A. NavonAL Goldberg2001Proteins are unfolded on the surface of the ATPase ring before transport into the proteasome.Mol Cell813391349
  22. 22. Pickart CM, VanDemark AP (2000) Opening doors into the proteasome. Nat Struct Mol Bio 7: 999–1001.CM PickartAP VanDemark2000Opening doors into the proteasome.Nat Struct Mol Bio79991001
  23. 23. Kenniston JA, Baker TA, Sauer RT (2005) Partitioning between unfolding and release of native domains during ClpXP degradation determines substrate selectivity and partial processing. Proc Natl Acad Sci U S A 102: 1390–1395.JA KennistonTA BakerRT Sauer2005Partitioning between unfolding and release of native domains during ClpXP degradation determines substrate selectivity and partial processing.Proc Natl Acad Sci U S A10213901395
  24. 24. Neira JL, Fersht AR (1999) Exploring the folding funnel of a polypeptide chain by biophysical studies on protein fragments. J Mol Biol 285: 1309–1333.JL NeiraAR Fersht1999Exploring the folding funnel of a polypeptide chain by biophysical studies on protein fragments.J Mol Biol28513091333
  25. 25. Clough RC, Vierstra RD (1997) Phytochrome degradation. Plant Cell Environ 20: 713–721.RC CloughRD Vierstra1997Phytochrome degradation.Plant Cell Environ20713721
  26. 26. Biou V, Dumas R, Cohen-Addad C, Douce R, Job D, et al. (1997) The crystal structure of plant acetohydroxy acid isomeroreductase complexed with NADPH, two magnesium ions and a herbicidal transition state analog determined at 1.65 A resolution. EMBO J 16: 3405–3415.V. BiouR. DumasC. Cohen-AddadR. DouceD. Job1997The crystal structure of plant acetohydroxy acid isomeroreductase complexed with NADPH, two magnesium ions and a herbicidal transition state analog determined at 1.65 A resolution.EMBO J1634053415
  27. 27. Fu Z, Hu Y, Markham GD, Takusagawa F (1996) Flexible loop in the structure of S-adenosylmethionine synthetase crystallized in the tetragonal modification. J Biomol Struct Dyn 13: 727–739.Z. FuY. HuGD MarkhamF. Takusagawa1996Flexible loop in the structure of S-adenosylmethionine synthetase crystallized in the tetragonal modification.J Biomol Struct Dyn13727739
  28. 28. Gonzalez B, Pajares MA, Hermoso JA, Alvarez L, Garrido F, et al. (2000) The crystal structure of tetrameric methionine adenosyltransferase from rat liver reveals the methionine-binding site. J Mol Biol 300: 363–375.B. GonzalezMA PajaresJA HermosoL. AlvarezF. Garrido2000The crystal structure of tetrameric methionine adenosyltransferase from rat liver reveals the methionine-binding site.J Mol Biol300363375
  29. 29. Sander C, Schneider R (1991) Database of homology-derived protein structures. Proteins: Struct Funct Genet 9: 56–68.C. SanderR. Schneider1991Database of homology-derived protein structures.Proteins: Struct Funct Genet95668
  30. 30. Morizono H, Cabrera-Luque J, Shi D, Gallegos R, Yamaguchi S, et al. (2006) Acetylornithine transcarbamylase: A novel enzyme in arginine biosynthesis. J Bacteriol 188: 2974–2982.H. MorizonoJ. Cabrera-LuqueD. ShiR. GallegosS. Yamaguchi2006Acetylornithine transcarbamylase: A novel enzyme in arginine biosynthesis.J Bacteriol18829742982
  31. 31. Shi D, Morizono H, Aoyagi M, Tuchman M, Allewell NM (2000) Crystal structure of human ornithine transcarbamylase complexed with carbamyl phosphate and L-Norvaline at 1.9 A resolution. Proteins: Struct Funct Genet 39: 271–277.D. ShiH. MorizonoM. AoyagiM. TuchmanNM Allewell2000Crystal structure of human ornithine transcarbamylase complexed with carbamyl phosphate and L-Norvaline at 1.9 A resolution.Proteins: Struct Funct Genet39271277
  32. 32. Villeret V, Clantin B, Tricot C, Legrain C, Roovers M, et al. (1998) The crystal structure of Pyrococcus furiosus ornithine carbamoyltransferase reveals a key role for oligomerization in enzyme stability at extremely high temperatures. Proc Natl Acad Sci U S A 95: 2801–2806.V. VilleretB. ClantinC. TricotC. LegrainM. Roovers1998The crystal structure of Pyrococcus furiosus ornithine carbamoyltransferase reveals a key role for oligomerization in enzyme stability at extremely high temperatures.Proc Natl Acad Sci U S A9528012806
  33. 33. Arsuaga J, Vasquez M, Trigueros S, Sumners DW, Roca J (2002) Knotting probability of DNA molecules confined in restricted volumes: DNA knotting in phage capsids. Proc Natl Acad Sci U S A 99: 5373–5377.J. ArsuagaM. VasquezS. TriguerosDW SumnersJ. Roca2002Knotting probability of DNA molecules confined in restricted volumes: DNA knotting in phage capsids.Proc Natl Acad Sci U S A9953735377
  34. 34. Janse van Rensburg EJ, Sumners DW, Wassermann E, Whittington SG (1992) Math Gen. 25. : 6557–6566.EJ Janse van RensburgDW SumnersE. WassermannSG Whittington1992Math Gen2565576566
  35. 35. Deguchi T, Tsurusaki K (1997) Universality in random knotting. Phys Rev E 55: 6245–6248.T. DeguchiK. Tsurusaki1997Universality in random knotting.Phys Rev E5562456248
  36. 36. Koniaris K, Muthukumar M (1991) Self-entanglement in ring polymers. J Chem Phys 95: 2873–2881.K. KoniarisM. Muthukumar1991Self-entanglement in ring polymers.J Chem Phys9528732881
  37. 37. Jackson SE, Mallam AL (2005) Folding studies on a knotted protein. J Mol Biol 346: 1409–1421.SE JacksonAL Mallam2005Folding studies on a knotted protein.J Mol Biol34614091421
  38. 38. Mallam AL, Jackson SE (2006) Probing nature's knots: The folding pathway of a knotted homodimeric protein. J Mol Biol 359: 1420–1436.AL MallamSE Jackson2006Probing nature's knots: The folding pathway of a knotted homodimeric protein.J Mol Biol35914201436
  39. 39. Millett K, Dobay A, Stasiak A (2005) Linear random knots and their scaling behavior. Macromolecules 38: 601–606.K. MillettA. DobayA. Stasiak2005Linear random knots and their scaling behavior.Macromolecules38601606
  40. 40. Das C, Hoang QQ, Kreinbring CA, Luchansky SJ, Meray RK, et al. (2006) Structural basis for conformational plasticity of the Parkinson's disease-associated ubiquitin hydrolase UCH-L1. Proc Natl Acad Sci U S A 103: 4675–4680.C. DasQQ HoangCA KreinbringSJ LuchanskyRK Meray2006Structural basis for conformational plasticity of the Parkinson's disease-associated ubiquitin hydrolase UCH-L1.Proc Natl Acad Sci U S A10346754680
  41. 41. Krissinel E, Henrick K (2004) Secondary-structure matching (SSM), a new tool for fast protein structure alignment in three dimensions. Acta Cryst D60: 2256–2268.E. KrissinelK. Henrick2004Secondary-structure matching (SSM), a new tool for fast protein structure alignment in three dimensions.Acta CrystD6022562268
  42. 42. Wilkinson KD, Lee KM, Deshpande S, Duerksen-Hughes P, Boss JM, et al. (1989) The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase. Science 246: 670–673.KD WilkinsonKM LeeS. DeshpandeP. Duerksen-HughesJM Boss1989The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase.Science246670673
  43. 43. Humphrey W, Dalke A, Schulten K (1996) VMD—Visual molecular dynamics. J Molec Graphics 14: 33–38.W. HumphreyA. DalkeK. Schulten1996VMD—Visual molecular dynamics.J Molec Graphics143338