2.350 Å
X-ray
2012-12-06
Name: | Tyrosine-protein kinase JAK3 |
---|---|
ID: | JAK3_HUMAN |
AC: | P52333 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | 2.7.10.2 |
Chain Name: | Percentage of Residues within binding site |
---|---|
B | 90 % |
C | 10 % |
B-Factor: | 35.868 |
---|---|
Number of residues: | 31 |
Including | |
Standard Amino Acids: | 30 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 1 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
1.001 | 1073.250 |
% Hydrophobic | % Polar |
---|---|
37.11 | 62.89 |
According to VolSite |
HET Code: | 1NX |
---|---|
Formula: | C23H25N5O3 |
Molecular weight: | 419.476 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 58.32 % |
Polar Surface area: | 108.99 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 5 |
H-Bond Donors: | 3 |
Rings: | 5 |
Aromatic rings: | 3 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 6 |
X | Y | Z |
---|---|---|
13.0141 | 25.405 | 46.7826 |
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 |
C18 | CD2 | LEU- 828 | 4.44 | 0 | Hydrophobic |
C24 | CD2 | LEU- 828 | 4.46 | 0 | Hydrophobic |
N22 | O | LEU- 828 | 2.89 | 159.52 | H-Bond (Ligand Donor) |
C1 | CG2 | VAL- 836 | 4.17 | 0 | Hydrophobic |
N9 | O | GLU- 903 | 2.84 | 158.38 | H-Bond (Ligand Donor) |
N11 | N | LEU- 905 | 3.11 | 176.29 | H-Bond (Protein Donor) |
C28 | SG | CYS- 909 | 3.99 | 0 | Hydrophobic |
C29 | CB | CYS- 909 | 3.55 | 0 | Hydrophobic |
C24 | CD | ARG- 916 | 3.49 | 0 | Hydrophobic |
C30 | CD2 | LEU- 956 | 3.81 | 0 | Hydrophobic |
C32 | CD2 | LEU- 956 | 4.08 | 0 | Hydrophobic |
C33 | CB | ALA- 966 | 4.02 | 0 | Hydrophobic |
C33 | CB | ASP- 967 | 3.73 | 0 | Hydrophobic |