1.480 Å
X-ray
2008-06-04
Min | Mean | Median | Standard Deviation | Max | Count | |
---|---|---|---|---|---|---|
pChEMBL: | 5.100 | 8.060 | 8.100 | 0.420 | 9.310 | 101 |
Name: | Carbonic anhydrase 2 |
---|---|
ID: | CAH2_HUMAN |
AC: | P00918 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | 4.2.1.1 |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 12.459 |
---|---|
Number of residues: | 26 |
Including | |
Standard Amino Acids: | 24 |
Non Standard Amino Acids: | 1 |
Water Molecules: | 1 |
Cofactors: | |
Metals: | ZN |
Ligandability | Volume (Å3) |
---|---|
0.712 | 354.375 |
% Hydrophobic | % Polar |
---|---|
53.33 | 46.67 |
According to VolSite |
HET Code: | EZL |
---|---|
Formula: | C9H10N2O3S2 |
Molecular weight: | 258.317 g/mol |
DrugBank ID: | DB00311 |
Buried Surface Area: | 59.35 % |
Polar Surface area: | 118.9 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 4 |
H-Bond Donors: | 1 |
Rings: | 2 |
Aromatic rings: | 2 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 3 |
X | Y | Z |
---|---|---|
-4.25406 | 3.702 | 15.2003 |
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 |
S2 | CG2 | VAL- 121 | 3.82 | 0 | Hydrophobic |
C9 | CE2 | PHE- 131 | 4.08 | 0 | Hydrophobic |
C3 | CD2 | LEU- 198 | 3.9 | 0 | Hydrophobic |
C7 | CD1 | LEU- 198 | 3.89 | 0 | Hydrophobic |
N1 | OG1 | THR- 199 | 2.82 | 164.18 | H-Bond (Ligand Donor) |
O1 | N | THR- 199 | 3.06 | 149.68 | H-Bond (Protein Donor) |
C7 | CB | THR- 200 | 4.27 | 0 | Hydrophobic |
C9 | CG | PRO- 202 | 4.41 | 0 | Hydrophobic |
N1 | ZN | ZN- 262 | 2.01 | 0 | Metal Acceptor |