sc-PDB
An Annotated Database of Druggable Binding Sites from the Protein DataBank
An Annotated Database of Druggable Binding Sites from the Protein DataBank
2.900 Å
X-ray
1999-05-25
| Name: | Peptidyl-prolyl cis-trans isomerase FKBP1A |
|---|---|
| ID: | FKB1A_HUMAN |
| AC: | P62942 |
| Organism: | Homo sapiens |
| Reign: | Eukaryota |
| TaxID: | 9606 |
| EC Number: | 5.2.1.8 |
| Chain Name: | Percentage of Residues within binding site |
|---|---|
| A | 81 % |
| C | 19 % |
| B-Factor: | 47.834 |
|---|---|
| Number of residues: | 31 |
| Including | |
| Standard Amino Acids: | 31 |
| Non Standard Amino Acids: | 0 |
| Water Molecules: | 0 |
| Cofactors: | |
| Metals: | |
| Ligandability | Volume (Å3) |
|---|---|
| 0.631 | 580.500 |
| % Hydrophobic | % Polar |
|---|---|
| 41.86 | 58.14 |
| According to VolSite | |
| HET Code: | 587 |
|---|---|
| Formula: | C52H76N2O13 |
| Molecular weight: | 937.165 g/mol |
| DrugBank ID: | DB03621 |
| Buried Surface Area: | 37.87 % |
| Polar Surface area: | 192.51 Å2 |
| Number of | |
|---|---|
| H-Bond Acceptors: | 13 |
| H-Bond Donors: | 3 |
| Rings: | 6 |
| Aromatic rings: | 2 |
| Anionic atoms: | 0 |
| Cationic atoms: | 0 |
| Rule of Five Violation: | 3 |
| Rotatable Bonds: | 8 |
| X | Y | Z |
|---|---|---|
| 44.7804 | 30.1863 | 7.34176 |
Image generated by PoseView
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 |
| C5 | CZ | TYR- 26 | 3.56 | 0 | Hydrophobic |
| O4 | OH | TYR- 26 | 3.46 | 128.34 | H-Bond (Protein Donor) |
| C10 | CE1 | PHE- 36 | 4.19 | 0 | Hydrophobic |
| C35 | CE1 | PHE- 36 | 3.63 | 0 | Hydrophobic |
| C10 | CB | ASP- 37 | 4.49 | 0 | Hydrophobic |
| O6 | OD2 | ASP- 37 | 2.71 | 157.36 | H-Bond (Ligand Donor) |
| C17 | CE1 | PHE- 46 | 4.1 | 0 | Hydrophobic |
| C36 | CD1 | PHE- 46 | 3.58 | 0 | Hydrophobic |
| C41 | CZ | PHE- 46 | 3.88 | 0 | Hydrophobic |
| C4 | CE2 | PHE- 46 | 3.59 | 0 | Hydrophobic |
| C4 | CG1 | VAL- 55 | 3.87 | 0 | Hydrophobic |
| C3 | CD1 | ILE- 56 | 4.33 | 0 | Hydrophobic |
| C30 | CG2 | ILE- 56 | 4.06 | 0 | Hydrophobic |
| C45 | CG2 | ILE- 56 | 4.45 | 0 | Hydrophobic |
| O2 | N | ILE- 56 | 3.11 | 150.91 | H-Bond (Protein Donor) |
| C5 | CZ2 | TRP- 59 | 3.95 | 0 | Hydrophobic |
| C3 | CE2 | TRP- 59 | 3.45 | 0 | Hydrophobic |
| C35 | CZ | TYR- 82 | 4.49 | 0 | Hydrophobic |
| C42 | CE2 | TYR- 82 | 4.17 | 0 | Hydrophobic |
| C45 | CD2 | TYR- 82 | 4.01 | 0 | Hydrophobic |
| C30 | CE2 | TYR- 82 | 3.75 | 0 | Hydrophobic |
| O3 | OH | TYR- 82 | 2.69 | 158.71 | H-Bond (Protein Donor) |
| C35 | CD1 | ILE- 91 | 3.24 | 0 | Hydrophobic |
| C44 | CB | SER- 208 | 3.81 | 0 | Hydrophobic |
| O8 | OG | SER- 208 | 2.92 | 167.96 | H-Bond (Protein Donor) |
