3.000 Å
X-ray
2007-05-18
Name: | Fibroblast growth factor receptor 2 |
---|---|
ID: | FGFR2_HUMAN |
AC: | P21802 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 28.485 |
---|---|
Number of residues: | 16 |
Including | |
Standard Amino Acids: | 16 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.649 | 408.375 |
% Hydrophobic | % Polar |
---|---|
60.33 | 39.67 |
According to VolSite |
HET Code: | ACP |
---|---|
Formula: | C11H14N5O12P3 |
Molecular weight: | 501.176 g/mol |
DrugBank ID: | DB03909 |
Buried Surface Area: | 54.33 % |
Polar Surface area: | 310.64 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 16 |
H-Bond Donors: | 3 |
Rings: | 3 |
Aromatic rings: | 2 |
Anionic atoms: | 4 |
Cationic atoms: | 0 |
Rule of Five Violation: | 2 |
Rotatable Bonds: | 8 |
X | Y | Z |
---|---|---|
29.9931 | 14.1327 | 24.7966 |
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 |
C5 | CD1 | LEU- 487 | 3.83 | 0 | Hydrophobic |
C5 | CG1 | VAL- 495 | 4.18 | 0 | Hydrophobic |
N6 | O | GLU- 565 | 3.14 | 132.69 | H-Bond (Ligand Donor) |
N1 | N | ALA- 567 | 3.2 | 153.34 | H-Bond (Protein Donor) |
C5 | CD1 | LEU- 633 | 3.37 | 0 | Hydrophobic |