2.300 Å
X-ray
2007-10-29
Name: | Three-prime repair exonuclease 1 |
---|---|
ID: | TREX1_MOUSE |
AC: | Q91XB0 |
Organism: | Mus musculus |
Reign: | Eukaryota |
TaxID: | 10090 |
EC Number: | 3.1.11.2 |
Chain Name: | Percentage of Residues within binding site |
---|---|
C | 100 % |
B-Factor: | 28.547 |
---|---|
Number of residues: | 28 |
Including | |
Standard Amino Acids: | 22 |
Non Standard Amino Acids: | 2 |
Water Molecules: | 4 |
Cofactors: | |
Metals: | ZN NA |
Ligandability | Volume (Å3) |
---|---|
0.540 | 465.750 |
% Hydrophobic | % Polar |
---|---|
44.20 | 55.80 |
According to VolSite |
HET Code: | TMP |
---|---|
Formula: | C10H13N2O8P |
Molecular weight: | 320.193 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 54.1 % |
Polar Surface area: | 161.1 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 8 |
H-Bond Donors: | 2 |
Rings: | 2 |
Aromatic rings: | 0 |
Anionic atoms: | 2 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 4 |
X | Y | Z |
---|---|---|
58.8011 | -3.89533 | -6.05586 |
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 |
O3' | OE1 | GLU- 20 | 2.84 | 163.16 | H-Bond (Ligand Donor) |
O3' | N | ALA- 21 | 2.7 | 170.88 | H-Bond (Protein Donor) |
C2' | CB | ALA- 81 | 4.06 | 0 | Hydrophobic |
C2' | CD1 | ILE- 84 | 4.3 | 0 | Hydrophobic |
C5M | CD1 | ILE- 84 | 4.21 | 0 | Hydrophobic |
C3' | CG2 | THR- 85 | 4.01 | 0 | Hydrophobic |
C5' | CE2 | TYR- 129 | 3.81 | 0 | Hydrophobic |
C4' | CZ | TYR- 129 | 3.76 | 0 | Hydrophobic |
C1' | CZ | TYR- 129 | 4.43 | 0 | Hydrophobic |
O3P | ZN | ZN- 800 | 2.14 | 0 | Metal Acceptor |