1.400 Å
X-ray
2002-05-21
Name: | Phenylalanine-4-hydroxylase |
---|---|
ID: | PH4H_CHRVO |
AC: | P30967 |
Organism: | Chromobacterium violaceum |
Reign: | Bacteria |
TaxID: | 243365 |
EC Number: | 1.14.16.1 |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 18.772 |
---|---|
Number of residues: | 26 |
Including | |
Standard Amino Acids: | 25 |
Non Standard Amino Acids: | 1 |
Water Molecules: | 0 |
Cofactors: | |
Metals: | FE |
Ligandability | Volume (Å3) |
---|---|
0.241 | 344.250 |
% Hydrophobic | % Polar |
---|---|
50.98 | 49.02 |
According to VolSite |
HET Code: | HBI |
---|---|
Formula: | C9H13N5O3 |
Molecular weight: | 239.231 g/mol |
DrugBank ID: | DB04400 |
Buried Surface Area: | 62.82 % |
Polar Surface area: | 132.33 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 7 |
H-Bond Donors: | 5 |
Rings: | 2 |
Aromatic rings: | 0 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 2 |
X | Y | Z |
---|---|---|
-16.1684 | 11.0303 | 26.7459 |
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 |
N2 | O | GLY- 100 | 3.11 | 128.75 | H-Bond (Ligand Donor) |
N1 | N | ILE- 102 | 3.18 | 172.09 | H-Bond (Protein Donor) |
N8 | O | ILE- 102 | 2.96 | 163.69 | H-Bond (Ligand Donor) |
O9 | OD1 | ASP- 104 | 3.33 | 174.17 | H-Bond (Ligand Donor) |
C7 | CG | PHE- 107 | 3.9 | 0 | Hydrophobic |
C11 | CE2 | PHE- 107 | 3.79 | 0 | Hydrophobic |
C10 | CB | ALA- 176 | 4.23 | 0 | Hydrophobic |
C11 | CG | TYR- 179 | 3.74 | 0 | Hydrophobic |