Figure 1.
An overview of the protein pocket-ligand interactions.
The top layer divides protein-ligand complexes into 5 major groups based on the type of the ligand. The second layer shows the major forces that are involved in formation of protein-ligand complexes for each type of the ligand. The bottom layer summarizes significant (frequently occurring) patterns for each force/bond type and each type of the ligand. The patterns are shown in XR…YL or XR – YL format where X denotes an atom type of residue R in the protein, Y denotes an atom type of the ligand L, strong interactions (covalent and coordination bonds) are depicted by “–”, and weak interactions (hydrogen bond) are represented by “…”.
Figure 2.
The summary of forces/bonds that are involved in formation of protein-organic compound complexes.
The chart shows that most of the complexes involve multiple contact types with the most frequent contacts involving both van der Waals force and hydrogen bonds.
Table 1.
A summary of interaction patterns concerning covalent bonds formed between a protein and an organic compound.
Table 2.
A summary of hydrogen bonds formed between specific amino acids and organic compounds.
Figure 3.
An example stereo diagram of hydrogen bonds formed between NH- group of a residue and oxygen atom of an organic compound.
The oxygen atom is colored red, nitrogen atom is blue, carbon atom is gray, and hydrogen atom is white. The residues in the pocket are in ball and stick format while the ligand is in stick format. Hydrogen bonds are represented by “…”. The structure is taken from chain A of neuraminidase protein (PDB entry 1F8E), which interacts with 49A. The binding pocket contains four Arg residues and each residue contains 2 NH- groups. Three Arg residues (Arg118, Arg292, Arg371) are spatially adjacent, and they form five hydrogen bonds with the oxygen atoms of the ligand.
Table 3.
A summary of the coordination bonds between metal ions and a given number of residues in a protein pocket that contribute at least one atom to form the bond.
Figure 4.
The residue groups that are coordinated by at least 10 metal ions and consist of 4 residues.
Figure 5.
The residue groups that are coordinated by at least 10 metal ions and consist of 3 residues.
Figure 6.
The residue groups that are coordinated by at least 10 metal ions and consist of 2 residues.
Figure 7.
Examples of typical coordination bonds between metal ions and Cys and His residues.
Coordination bonds are represented by solid lines; the dashed lines show the distance between atoms of different residues. Panel A shows the coordination bond between zinc ion and four Cys residues where sulfur atom is shown in gray, carbon atom in white, and zinc ion in black. The sulfur atoms of four Cys residues form an approximate regular tetrahedron and the zinc ion is located in its center. Panel B shows the coordination bond between zinc ion and three His residues. The nitrogen atoms are shown in gray, other atoms of the His side chain are in white, and zinc ion is colored black. The three nitrogen atoms form an approximate equilateral triangle with the length of the sides that varies between 3.14 Å and 3.31 Å. The zinc ion is not located on the triangle plane.
Figure 8.
Percentage of occurrence of amino acids in the protein-organic compound binding pockets (gray bar) and in protein-protein interaction interfaces (black bar).
Figure 9.
Performance of blind binding site predictors including the pattern-based method, LigsiteCSC, and a random baseline predictor.
The y axis shows success rate, i.e., fraction of proteins with minimum distance between the top five predicted binding sites and any atom of a ligand in the native complex that is smaller or equal to the distance displayed on the x axis. The five plots concern the scanning method based solely on the hydrogen bond pattern (named “Scanning (hydrogen)”), the scanning method based on the four patterns concerning both hydrogen and covalent bonds (named “Scanning (hydrogen&covalent)”), the result of LigsiteCSC, the result of baseline method that randomly picks 5 solvent grid points that are within 5Å from the protein surface (named “Random baseline”), and the results that merge the top two predictions of LigsiteCSC and the top three predictions of the scanning method that uses the four patterns (named “Scanning/Ligsite-csc hybrid”).
Figure 10.
The structure of Anguilla anguilla agglutinin protein (PDB entry 1K12).
The binding sites predicted by Ligsite CSC are colored in green and the binding sites predicted by the pattern-based method are colored in blue. The protein surface is rendered in gray and the ligand is in the stick form. The LigsiteCSC predictions are over 10Å away from any atom of the ligand, while one of pattern-based predictions is 0.67Å away from one of the ligand's atoms. Only 4 predictions by Ligsite CSC and by the pattern-based method are visible; the remaining predictions are on the other side of the protein.