2.670 Å
X-ray
2000-05-19
Name: | Glutamine synthetase |
---|---|
ID: | GLNA_SALTY |
AC: | P0A1P6 |
Organism: | Salmonella typhimurium |
Reign: | Bacteria |
TaxID: | 99287 |
EC Number: | 6.3.1.2 |
Chain Name: | Percentage of Residues within binding site |
---|---|
H | 11 % |
I | 89 % |
B-Factor: | 48.176 |
---|---|
Number of residues: | 39 |
Including | |
Standard Amino Acids: | 36 |
Non Standard Amino Acids: | 2 |
Water Molecules: | 1 |
Cofactors: | |
Metals: | MN MN |
Ligandability | Volume (Å3) |
---|---|
0.349 | 2241.000 |
% Hydrophobic | % Polar |
---|---|
41.42 | 58.58 |
According to VolSite |
HET Code: | ADP |
---|---|
Formula: | C10H12N5O10P2 |
Molecular weight: | 424.177 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 60.76 % |
Polar Surface area: | 260.7 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 14 |
H-Bond Donors: | 3 |
Rings: | 3 |
Aromatic rings: | 2 |
Anionic atoms: | 3 |
Cationic atoms: | 0 |
Rule of Five Violation: | 1 |
Rotatable Bonds: | 6 |
X | Y | Z |
---|---|---|
-34.6415 | 46.4319 | -17.7734 |
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' | CG | GLU- 129 | 4.1 | 0 | Hydrophobic |
O2' | OE1 | GLU- 207 | 3.23 | 147.75 | H-Bond (Ligand Donor) |
O2B | NE2 | HIS- 210 | 2.83 | 165.58 | H-Bond (Protein Donor) |
O3' | O | THR- 223 | 2.55 | 144.66 | H-Bond (Ligand Donor) |
C2' | CD1 | PHE- 225 | 4.25 | 0 | Hydrophobic |
C1' | CB | PHE- 225 | 3.97 | 0 | Hydrophobic |
O2' | N | PHE- 225 | 3.22 | 155.11 | H-Bond (Protein Donor) |
C1' | CB | HIS- 271 | 3.95 | 0 | Hydrophobic |