sc-PDB
An Annotated Database of Druggable Binding Sites from the Protein DataBank
An Annotated Database of Druggable Binding Sites from the Protein DataBank
1.550 Å
X-ray
2002-09-24
| Name: | GDP-mannose 6-dehydrogenase |
|---|---|
| ID: | ALGD_PSEAE |
| AC: | P11759 |
| Organism: | Pseudomonas aeruginosa |
| Reign: | Bacteria |
| TaxID: | 208964 |
| EC Number: | 1.1.1.132 |
| Chain Name: | Percentage of Residues within binding site |
|---|---|
| A | 47 % |
| B | 53 % |
| B-Factor: | 8.060 |
|---|---|
| Number of residues: | 45 |
| Including | |
| Standard Amino Acids: | 42 |
| Non Standard Amino Acids: | 1 |
| Water Molecules: | 2 |
| Cofactors: | NAD |
| Metals: | |
| Ligandability | Volume (Å3) |
|---|---|
| 0.957 | 715.500 |
| % Hydrophobic | % Polar |
|---|---|
| 42.92 | 57.08 |
| According to VolSite | |
| HET Code: | GDX |
|---|---|
| Formula: | C16H20N5O17P2 |
| Molecular weight: | 616.301 g/mol |
| DrugBank ID: | DB04023 |
| Buried Surface Area: | 73.47 % |
| Polar Surface area: | 372.61 Å2 |
| Number of | |
|---|---|
| H-Bond Acceptors: | 20 |
| H-Bond Donors: | 7 |
| Rings: | 4 |
| Aromatic rings: | 1 |
| Anionic atoms: | 3 |
| Cationic atoms: | 0 |
| Rule of Five Violation: | 3 |
| Rotatable Bonds: | 9 |
| X | Y | Z |
|---|---|---|
| -42.693 | 6.76743 | -21.9194 |
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 |
| O4' | O | LEU- 159 | 2.77 | 160.1 | H-Bond (Ligand Donor) |
| C3' | CG | ARG- 160 | 3.95 | 0 | Hydrophobic |
| O2B | N | GLU- 161 | 2.97 | 160.98 | H-Bond (Protein Donor) |
| O6A | NZ | LYS- 210 | 2.87 | 157.84 | H-Bond (Protein Donor) |
| O6A | NZ | LYS- 210 | 2.87 | 0 | Ionic (Protein Cationic) |
| O6A | ND2 | ASN- 214 | 2.85 | 165.22 | H-Bond (Protein Donor) |
| O2' | OD1 | ASN- 214 | 2.69 | 144.28 | H-Bond (Ligand Donor) |
| C1D | CG2 | VAL- 221 | 4.45 | 0 | Hydrophobic |
| O2A | OH | TYR- 256 | 2.66 | 162.85 | H-Bond (Protein Donor) |
| O1A | OH | TYR- 257 | 2.56 | 167.37 | H-Bond (Protein Donor) |
| N2 | O | ARG- 259 | 3.29 | 129.12 | H-Bond (Ligand Donor) |
| N1 | O | ARG- 259 | 2.59 | 174.78 | H-Bond (Ligand Donor) |
| O6 | N | ARG- 259 | 2.98 | 154.23 | H-Bond (Protein Donor) |
| N2 | O | PHE- 262 | 3.04 | 171.41 | H-Bond (Ligand Donor) |
| C1D | CB | PHE- 264 | 4.43 | 0 | Hydrophobic |
| C4D | CB | PHE- 264 | 3.94 | 0 | Hydrophobic |
| O3D | N | GLY- 265 | 2.85 | 140.46 | H-Bond (Protein Donor) |
| C5' | CB | CYS- 268 | 4.26 | 0 | Hydrophobic |
| C5D | CD2 | LEU- 269 | 4 | 0 | Hydrophobic |
| C1' | CD1 | LEU- 269 | 3.81 | 0 | Hydrophobic |
| C3D | CD2 | PHE- 323 | 3.83 | 0 | Hydrophobic |
| C5D | CE2 | PHE- 323 | 3.87 | 0 | Hydrophobic |
| O2A | NZ | LYS- 324 | 2.81 | 151.98 | H-Bond (Protein Donor) |
| O3A | NZ | LYS- 324 | 3.31 | 140.22 | H-Bond (Protein Donor) |
| O2A | NZ | LYS- 324 | 2.81 | 0 | Ionic (Protein Cationic) |
| C3D | CG | LYS- 324 | 4.34 | 0 | Hydrophobic |
| O3B | O | HOH- 2031 | 2.68 | 179.95 | H-Bond (Protein Donor) |
