2.710 Å
X-ray
2015-08-04
Name: | Uncharacterized protein |
---|---|
ID: | C7Q5P8_CATAD |
AC: | C7Q5P8 |
Organism: | Catenulispora acidiphila |
Reign: | Bacteria |
TaxID: | 479433 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 38.131 |
---|---|
Number of residues: | 32 |
Including | |
Standard Amino Acids: | 32 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.306 | 479.250 |
% Hydrophobic | % Polar |
---|---|
39.44 | 60.56 |
According to VolSite |
HET Code: | SAH |
---|---|
Formula: | C14H20N6O5S |
Molecular weight: | 384.411 g/mol |
DrugBank ID: | DB01752 |
Buried Surface Area: | 67.55 % |
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 |
---|---|---|
-2.35869 | -3.39635 | 18.9483 |
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 |
N | O | GLY- 38 | 2.99 | 175.89 | H-Bond (Ligand Donor) |
O3' | OD2 | ASP- 61 | 3.43 | 153.08 | H-Bond (Ligand Donor) |
O2' | OD2 | ASP- 61 | 3.25 | 144.55 | H-Bond (Ligand Donor) |
O2' | OD1 | ASP- 61 | 2.83 | 143.75 | H-Bond (Ligand Donor) |
N1 | N | ILE- 93 | 3.39 | 167.34 | H-Bond (Protein Donor) |
N6 | OE1 | GLU- 94 | 3.19 | 164.36 | H-Bond (Ligand Donor) |
C5' | CB | TRP- 113 | 4.05 | 0 | Hydrophobic |
N7 | N | LEU- 116 | 3.31 | 144.47 | H-Bond (Protein Donor) |
O | OG | SER- 200 | 2.97 | 141.08 | H-Bond (Protein Donor) |
OXT | OG | SER- 200 | 3.29 | 160.12 | H-Bond (Protein Donor) |
OXT | N | SER- 201 | 3.36 | 158.82 | H-Bond (Protein Donor) |