2.350 Å
X-ray
2003-09-22
Name: | Prolyl endopeptidase |
---|---|
ID: | PPCE_PIG |
AC: | P23687 |
Organism: | Sus scrofa |
Reign: | Eukaryota |
TaxID: | 9823 |
EC Number: | 3.4.21.26 |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 26.835 |
---|---|
Number of residues: | 27 |
Including | |
Standard Amino Acids: | 27 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.647 | 479.250 |
% Hydrophobic | % Polar |
---|---|
43.66 | 56.34 |
According to VolSite |
HET Code: | GLY_PHE_ARG_PRO |
---|---|
Formula: | C22H34N7O5 |
Molecular weight: | 476.549 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 50.37 % |
Polar Surface area: | 212.28 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 5 |
H-Bond Donors: | 6 |
Rings: | 2 |
Aromatic rings: | 1 |
Anionic atoms: | 1 |
Cationic atoms: | 2 |
Rule of Five Violation: | 2 |
Rotatable Bonds: | 12 |
X | Y | Z |
---|---|---|
40.6419 | 37.0191 | 85.0594 |
Represent the protein/ligand binding mode, centered on the ligand
Dashed lines represents hydrogen bonds and metal interactions
Green residue labels for amino acids with hydrophobic contacts (green lines) to the ligand
Ligand | Protein | Interaction | |||
---|---|---|---|---|---|
Atom | Atom | Residue | Distance (Å) | Angle (°) | Type |
CB | CE1 | PHE- 173 | 3.72 | 0 | Hydrophobic |
CD1 | CB | PHE- 173 | 4.13 | 0 | Hydrophobic |
CD1 | CE | MET- 235 | 3.78 | 0 | Hydrophobic |
CZ | SD | MET- 235 | 3.98 | 0 | Hydrophobic |
CG | SG | CYS- 255 | 4.07 | 0 | Hydrophobic |
CD2 | SG | CYS- 255 | 3.95 | 0 | Hydrophobic |
CG | CZ | PHE- 476 | 3.61 | 0 | Hydrophobic |
CG | CD1 | PHE- 476 | 4.22 | 0 | Hydrophobic |
CD | CD1 | ILE- 478 | 3.97 | 0 | Hydrophobic |
CB | CB | ALA- 554 | 3.94 | 0 | Hydrophobic |
O | N | ASN- 555 | 3.2 | 156.5 | H-Bond (Protein Donor) |
CG | CB | ASN- 555 | 4.42 | 0 | Hydrophobic |
CB | CG2 | VAL- 580 | 4.13 | 0 | Hydrophobic |
CB | CG1 | ILE- 591 | 3.67 | 0 | Hydrophobic |
CD2 | CB | ALA- 594 | 3.99 | 0 | Hydrophobic |
O | NE1 | TRP- 595 | 3.01 | 164.38 | H-Bond (Protein Donor) |
CB | CZ2 | TRP- 595 | 3.85 | 0 | Hydrophobic |
CG | CE2 | TRP- 595 | 3.63 | 0 | Hydrophobic |
O | NH1 | ARG- 643 | 2.69 | 145.36 | H-Bond (Protein Donor) |
CB | CG2 | VAL- 644 | 3.87 | 0 | Hydrophobic |
OXT | NE2 | HIS- 680 | 3.34 | 168.06 | H-Bond (Protein Donor) |