2.500 Å
X-ray
2003-05-12
Name: | tRNA (guanine-N(1)-)-methyltransferase |
---|---|
ID: | TRMD_ECOLI |
AC: | P0A873 |
Organism: | Escherichia coli |
Reign: | Bacteria |
TaxID: | 83333 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 50.143 |
---|---|
Number of residues: | 28 |
Including | |
Standard Amino Acids: | 28 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.505 | 320.625 |
% Hydrophobic | % Polar |
---|---|
37.89 | 62.11 |
According to VolSite |
HET Code: | SAH |
---|---|
Formula: | C14H20N6O5S |
Molecular weight: | 384.411 g/mol |
DrugBank ID: | DB01752 |
Buried Surface Area: | 71.17 % |
Polar Surface area: | 212.38 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 10 |
H-Bond Donors: | 4 |
Rings: | 3 |
Aromatic rings: | 2 |
Anionic atoms: | 1 |
Cationic atoms: | 1 |
Rule of Five Violation: | 1 |
Rotatable Bonds: | 7 |
X | Y | Z |
---|---|---|
33.6014 | 42.3237 | 39.644 |
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 |
C3' | CZ | TYR- 86 | 4.43 | 0 | Hydrophobic |
O3' | OH | TYR- 86 | 2.52 | 158.08 | H-Bond (Ligand Donor) |
CB | CG | PRO- 89 | 4.06 | 0 | Hydrophobic |
O2' | N | GLY- 113 | 3.2 | 142.71 | H-Bond (Protein Donor) |
N1 | N | ILE- 133 | 3.18 | 160.43 | H-Bond (Protein Donor) |
N6 | O | GLY- 134 | 3.05 | 120.6 | H-Bond (Ligand Donor) |
N6 | O | TYR- 136 | 2.94 | 160.78 | H-Bond (Ligand Donor) |
SD | CG1 | VAL- 137 | 4.06 | 0 | Hydrophobic |
N7 | N | LEU- 138 | 2.95 | 166.67 | H-Bond (Protein Donor) |