2.500 Å
X-ray
2011-05-06
Name: | Tyrosine-protein kinase JAK2 |
---|---|
ID: | JAK2_HUMAN |
AC: | O60674 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 35.256 |
---|---|
Number of residues: | 31 |
Including | |
Standard Amino Acids: | 31 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
1.083 | 435.375 |
% Hydrophobic | % Polar |
---|---|
54.26 | 45.74 |
According to VolSite |
HET Code: | 17P |
---|---|
Formula: | C22H24N6O |
Molecular weight: | 388.466 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 49.93 % |
Polar Surface area: | 101.62 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 4 |
H-Bond Donors: | 3 |
Rings: | 5 |
Aromatic rings: | 4 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 4 |
X | Y | Z |
---|---|---|
-24.824 | -35.4718 | 6.19279 |
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 |
C4 | CD1 | LEU- 855 | 4.12 | 0 | Hydrophobic |
C8 | CB | LEU- 855 | 3.92 | 0 | Hydrophobic |
C9 | CD2 | LEU- 855 | 3.99 | 0 | Hydrophobic |
C15 | CG2 | VAL- 863 | 4.3 | 0 | Hydrophobic |
C4 | CB | ALA- 880 | 3.88 | 0 | Hydrophobic |
N20 | O | GLU- 930 | 2.79 | 157.42 | H-Bond (Ligand Donor) |
C11 | CE1 | TYR- 931 | 3.8 | 0 | Hydrophobic |
N | O | LEU- 932 | 2.88 | 122.85 | H-Bond (Ligand Donor) |
O | N | LEU- 932 | 2.75 | 150.5 | H-Bond (Protein Donor) |
C4 | CD1 | LEU- 983 | 3.75 | 0 | Hydrophobic |
C19 | CD2 | LEU- 983 | 4.32 | 0 | Hydrophobic |
C18 | CB | ASP- 994 | 4.5 | 0 | Hydrophobic |