1.550 Å
X-ray
1999-09-28
Min | Mean | Median | Standard Deviation | Max | Count | |
---|---|---|---|---|---|---|
pChEMBL: | 9.740 | 9.740 | 9.740 | 0.000 | 9.740 | 1 |
Name: | Sex hormone-binding globulin |
---|---|
ID: | SHBG_HUMAN |
AC: | P04278 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 24.485 |
---|---|
Number of residues: | 32 |
Including | |
Standard Amino Acids: | 32 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
1.529 | 550.125 |
% Hydrophobic | % Polar |
---|---|
66.87 | 33.13 |
According to VolSite |
HET Code: | DHT |
---|---|
Formula: | C19H30O2 |
Molecular weight: | 290.440 g/mol |
DrugBank ID: | DB02901 |
Buried Surface Area: | 74.71 % |
Polar Surface area: | 37.29 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 2 |
H-Bond Donors: | 1 |
Rings: | 4 |
Aromatic rings: | 0 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 0 |
X | Y | Z |
---|---|---|
21.7863 | 10.7318 | 32.5236 |
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 |
O3 | OG | SER- 42 | 2.76 | 156.87 | H-Bond (Protein Donor) |
C4 | CE1 | PHE- 56 | 3.91 | 0 | Hydrophobic |
C6 | CE1 | PHE- 56 | 3.96 | 0 | Hydrophobic |
C16 | CB | ASP- 65 | 4.33 | 0 | Hydrophobic |
O17 | OD1 | ASP- 65 | 2.73 | 169.08 | H-Bond (Ligand Donor) |
C6 | CD2 | PHE- 67 | 3.89 | 0 | Hydrophobic |
C18 | CB | PHE- 67 | 4.02 | 0 | Hydrophobic |
C19 | CE1 | PHE- 67 | 3.64 | 0 | Hydrophobic |
C8 | CB | PHE- 67 | 3.75 | 0 | Hydrophobic |
C18 | CD1 | LEU- 80 | 4.2 | 0 | Hydrophobic |
O17 | ND2 | ASN- 82 | 2.93 | 156.28 | H-Bond (Protein Donor) |
C2 | CG1 | VAL- 105 | 4.2 | 0 | Hydrophobic |
C19 | CG1 | VAL- 105 | 3.94 | 0 | Hydrophobic |
C1 | CG | MET- 107 | 3.84 | 0 | Hydrophobic |
C11 | CG | MET- 107 | 3.91 | 0 | Hydrophobic |
C12 | SD | MET- 107 | 4.19 | 0 | Hydrophobic |
C11 | CG2 | VAL- 112 | 4.25 | 0 | Hydrophobic |
C19 | CG1 | VAL- 112 | 4.21 | 0 | Hydrophobic |
C7 | SD | MET- 139 | 4.12 | 0 | Hydrophobic |
C14 | CE | MET- 139 | 4.1 | 0 | Hydrophobic |
C6 | CD1 | ILE- 141 | 3.89 | 0 | Hydrophobic |
C4 | CD2 | LEU- 171 | 4.44 | 0 | Hydrophobic |