1.890 Å
X-ray
2013-10-09
| Name: | Glycylpeptide N-tetradecanoyltransferase |
|---|---|
| ID: | NMT_ASPFU |
| AC: | Q9UVX3 |
| Organism: | Neosartorya fumigata |
| Reign: | Eukaryota |
| TaxID: | 330879 |
| EC Number: | 2.3.1.97 |
| Chain Name: | Percentage of Residues within binding site |
|---|---|
| A | 100 % |
| B-Factor: | 19.114 |
|---|---|
| Number of residues: | 46 |
| Including | |
| Standard Amino Acids: | 44 |
| Non Standard Amino Acids: | 0 |
| Water Molecules: | 2 |
| Cofactors: | |
| Metals: | |
| Ligandability | Volume (Å3) |
|---|---|
| 1.671 | 438.750 |
| % Hydrophobic | % Polar |
|---|---|
| 75.38 | 24.62 |
| According to VolSite | |

| HET Code: | MYA |
|---|---|
| Formula: | C35H58N7O17P3S |
| Molecular weight: | 973.858 g/mol |
| DrugBank ID: | DB02180 |
| Buried Surface Area: | 63.13 % |
| Polar Surface area: | 429.68 Å2 |
| Number of | |
|---|---|
| H-Bond Acceptors: | 22 |
| H-Bond Donors: | 5 |
| Rings: | 3 |
| Aromatic rings: | 2 |
| Anionic atoms: | 4 |
| Cationic atoms: | 0 |
| Rule of Five Violation: | 2 |
| Rotatable Bonds: | 32 |
| X | Y | Z |
|---|---|---|
| -3.06451 | 7.99116 | -14.4034 |
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 |
| C2 | CZ | TYR- 147 | 3.94 | 0 | Hydrophobic |
| C6 | CD2 | TYR- 147 | 3.43 | 0 | Hydrophobic |
| C6M | CD1 | ILE- 193 | 4.35 | 0 | Hydrophobic |
| CCM | CG2 | VAL- 210 | 4.41 | 0 | Hydrophobic |
| CEM | CG2 | VAL- 210 | 4.1 | 0 | Hydrophobic |
| C8M | CG2 | ILE- 212 | 3.96 | 0 | Hydrophobic |
| CCM | CD1 | ILE- 212 | 3.7 | 0 | Hydrophobic |
| C5M | CG2 | ILE- 212 | 4.04 | 0 | Hydrophobic |
| CBM | CG1 | ILE- 212 | 3.91 | 0 | Hydrophobic |
| N4 | O | LEU- 215 | 2.73 | 175.33 | H-Bond (Ligand Donor) |
| C13 | CD2 | LEU- 215 | 3.98 | 0 | Hydrophobic |
| C14 | CG | LEU- 215 | 3.7 | 0 | Hydrophobic |
| C4M | CD2 | LEU- 215 | 3.89 | 0 | Hydrophobic |
| C6M | CD2 | LEU- 215 | 4.28 | 0 | Hydrophobic |
| O2M | N | LEU- 215 | 3.28 | 154.42 | H-Bond (Protein Donor) |
| O9 | N | ILE- 217 | 3 | 160.23 | H-Bond (Protein Donor) |
| C14 | CD1 | ILE- 217 | 3.67 | 0 | Hydrophobic |
| C10 | CD | ARG- 222 | 3.97 | 0 | Hydrophobic |
| O4A | N | SER- 223 | 2.81 | 153.25 | H-Bond (Protein Donor) |
| O1A | N | ARG- 225 | 2.72 | 147.62 | H-Bond (Protein Donor) |
| O7A | NH1 | ARG- 225 | 2.62 | 153.06 | H-Bond (Protein Donor) |
| O7A | NH2 | ARG- 225 | 3.47 | 121.59 | H-Bond (Protein Donor) |
| O8A | NH1 | ARG- 225 | 3.46 | 127.25 | H-Bond (Protein Donor) |
| O8A | NH2 | ARG- 225 | 2.79 | 152.75 | H-Bond (Protein Donor) |
| O7A | CZ | ARG- 225 | 3.44 | 0 | Ionic (Protein Cationic) |
| O8A | CZ | ARG- 225 | 3.54 | 0 | Ionic (Protein Cationic) |
| C12 | CB | THR- 227 | 4.43 | 0 | Hydrophobic |
| C1X | CG2 | THR- 227 | 3.84 | 0 | Hydrophobic |
| C4X | CB | THR- 227 | 4.24 | 0 | Hydrophobic |
| O2A | OG1 | THR- 227 | 2.92 | 147.42 | H-Bond (Protein Donor) |
| O2A | N | THR- 227 | 2.78 | 160.9 | H-Bond (Protein Donor) |
| CBM | CG2 | ILE- 231 | 4.17 | 0 | Hydrophobic |
| C7M | CG1 | ILE- 231 | 3.62 | 0 | Hydrophobic |
| C9M | CG2 | ILE- 231 | 3.8 | 0 | Hydrophobic |
| CBM | CG2 | ILE- 234 | 4.22 | 0 | Hydrophobic |
| CCM | CB | THR- 235 | 4.43 | 0 | Hydrophobic |
| CDM | CG2 | THR- 235 | 4.24 | 0 | Hydrophobic |
| CEM | CB | CYS- 238 | 3.55 | 0 | Hydrophobic |
| CFM | CE1 | TYR- 239 | 3.76 | 0 | Hydrophobic |
| CFM | CG2 | ILE- 243 | 4.45 | 0 | Hydrophobic |
| CCM | CB | ALA- 246 | 3.81 | 0 | Hydrophobic |
| CDM | CB | ALA- 246 | 3.68 | 0 | Hydrophobic |
| C7M | CZ | TYR- 248 | 3.95 | 0 | Hydrophobic |
| C9M | CE1 | TYR- 248 | 3.63 | 0 | Hydrophobic |
| C5M | CD2 | TYR- 248 | 3.44 | 0 | Hydrophobic |
| S1 | CB | ALA- 250 | 4.24 | 0 | Hydrophobic |
| C9M | CD1 | TYR- 462 | 4.3 | 0 | Hydrophobic |
| CAM | CB | TYR- 462 | 3.88 | 0 | Hydrophobic |
| CFM | CD2 | TYR- 462 | 3.47 | 0 | Hydrophobic |
| O4A | O | HOH- 2176 | 3.15 | 137.88 | H-Bond (Protein Donor) |