2.300 Å
X-ray
2011-03-25
Name: | Heat shock protein HSP 90-alpha |
---|---|
ID: | HS90A_HUMAN |
AC: | P07900 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 38.208 |
---|---|
Number of residues: | 28 |
Including | |
Standard Amino Acids: | 27 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 1 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.417 | 482.625 |
% Hydrophobic | % Polar |
---|---|
45.45 | 54.55 |
According to VolSite |
HET Code: | 2FY |
---|---|
Formula: | C9H10O3 |
Molecular weight: | 166.174 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 64.5 % |
Polar Surface area: | 57.53 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 3 |
H-Bond Donors: | 2 |
Rings: | 1 |
Aromatic rings: | 1 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 2 |
X | Y | Z |
---|---|---|
30.6185 | 10.5307 | 24.8837 |
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 |
O2 | ND2 | ASN- 51 | 3.3 | 157.68 | H-Bond (Protein Donor) |
C3 | CB | ASN- 51 | 3.41 | 0 | Hydrophobic |
C9 | CB | ALA- 55 | 3.59 | 0 | Hydrophobic |
C5 | CB | ALA- 55 | 4.26 | 0 | Hydrophobic |
O8 | OD2 | ASP- 93 | 2.6 | 162.67 | H-Bond (Ligand Donor) |
C7 | CG | MET- 98 | 3.51 | 0 | Hydrophobic |
C1 | CE | MET- 98 | 3.51 | 0 | Hydrophobic |
C5 | CB | THR- 184 | 3.95 | 0 | Hydrophobic |
C4 | CG2 | THR- 184 | 4.23 | 0 | Hydrophobic |
C10 | CG2 | THR- 184 | 4.38 | 0 | Hydrophobic |
O1 | OG1 | THR- 184 | 2.86 | 141.87 | H-Bond (Protein Donor) |
C3 | CG2 | VAL- 186 | 4.29 | 0 | Hydrophobic |