2.400 Å
X-ray
1996-06-25
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: | 14.434 |
---|---|
Number of residues: | 26 |
Including | |
Standard Amino Acids: | 25 |
Non Standard Amino Acids: | 1 |
Water Molecules: | 0 |
Cofactors: | |
Metals: | ZN |
Ligandability | Volume (Å3) |
---|---|
0.469 | 327.375 |
% Hydrophobic | % Polar |
---|---|
49.48 | 50.52 |
According to VolSite |
HET Code: | STB |
---|---|
Formula: | C12H20N3O3S2 |
Molecular weight: | 318.435 g/mol |
DrugBank ID: | DB04002 |
Buried Surface Area: | 48.47 % |
Polar Surface area: | 153.04 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 4 |
H-Bond Donors: | 4 |
Rings: | 1 |
Aromatic rings: | 1 |
Anionic atoms: | 0 |
Cationic atoms: | 1 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 8 |
X | Y | Z |
---|---|---|
-3.4085 | 5.7704 | 15.3726 |
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 |
C2 | CG1 | VAL- 121 | 4 | 0 | Hydrophobic |
C3 | CG2 | VAL- 121 | 3.47 | 0 | Hydrophobic |
C3' | CE2 | PHE- 131 | 4.14 | 0 | Hydrophobic |
C4 | CD2 | LEU- 198 | 3.54 | 0 | Hydrophobic |
O1S | N | THR- 199 | 3.47 | 141.88 | H-Bond (Protein Donor) |
N3S | OG1 | THR- 199 | 3.1 | 138.5 | H-Bond (Ligand Donor) |
C2' | CG | PRO- 202 | 3.88 | 0 | Hydrophobic |
S7' | CG | PRO- 202 | 3.74 | 0 | Hydrophobic |
N3S | ZN | ZN- 262 | 2.46 | 0 | Metal Acceptor |