1.280 Å
X-ray
2007-08-29
Name: | Cyclin-dependent kinase 2 |
---|---|
ID: | CDK2_HUMAN |
AC: | P24941 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | 2.7.11.22 |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 17.220 |
---|---|
Number of residues: | 29 |
Including | |
Standard Amino Acids: | 29 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.325 | 560.250 |
% Hydrophobic | % Polar |
---|---|
36.14 | 63.86 |
According to VolSite |
HET Code: | SCF |
---|---|
Formula: | C18H14FN5 |
Molecular weight: | 319.336 g/mol |
DrugBank ID: | DB08534 |
Buried Surface Area: | 63.67 % |
Polar Surface area: | 55.11 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 4 |
H-Bond Donors: | 1 |
Rings: | 4 |
Aromatic rings: | 4 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 4 |
X | Y | Z |
---|---|---|
1.70421 | 27.8739 | 8.04796 |
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 |
C14 | CB | ILE- 10 | 4.13 | 0 | Hydrophobic |
C18 | CD1 | ILE- 10 | 4.12 | 0 | Hydrophobic |
C19 | CG2 | VAL- 18 | 4 | 0 | Hydrophobic |
N06 | NZ | LYS- 33 | 2.96 | 147.48 | H-Bond (Protein Donor) |
N04 | N | LEU- 83 | 3.35 | 170.97 | H-Bond (Protein Donor) |
N10 | O | LEU- 83 | 2.78 | 126.11 | H-Bond (Ligand Donor) |
F24 | CB | ASN- 132 | 3.59 | 0 | Hydrophobic |
C12 | CD2 | LEU- 134 | 4.06 | 0 | Hydrophobic |
F24 | CB | ALA- 144 | 3.81 | 0 | Hydrophobic |