2.200 Å
X-ray
1998-07-31
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: | 13.424 |
---|---|
Number of residues: | 26 |
Including | |
Standard Amino Acids: | 25 |
Non Standard Amino Acids: | 1 |
Water Molecules: | 0 |
Cofactors: | |
Metals: | ZN |
Ligandability | Volume (Å3) |
---|---|
0.346 | 344.250 |
% Hydrophobic | % Polar |
---|---|
43.14 | 56.86 |
According to VolSite |
HET Code: | AL6 |
---|---|
Formula: | C13H12N2O5S3 |
Molecular weight: | 372.440 g/mol |
DrugBank ID: | DB04371 |
Buried Surface Area: | 56.1 % |
Polar Surface area: | 151.76 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 5 |
H-Bond Donors: | 1 |
Rings: | 3 |
Aromatic rings: | 2 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 3 |
X | Y | Z |
---|---|---|
-3.8843 | 5.1907 | 14.7713 |
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 | 3.72 | 0 | Hydrophobic |
C13 | CE2 | PHE- 131 | 3.5 | 0 | Hydrophobic |
C17 | CG2 | VAL- 135 | 3.62 | 0 | Hydrophobic |
C16 | CD1 | LEU- 198 | 4.06 | 0 | Hydrophobic |
S2 | CD2 | LEU- 198 | 3.59 | 0 | Hydrophobic |
O1A | N | THR- 199 | 2.79 | 160.74 | H-Bond (Protein Donor) |
N21 | OG1 | THR- 199 | 2.62 | 142.7 | H-Bond (Ligand Donor) |
C17 | CG | PRO- 202 | 4.44 | 0 | Hydrophobic |
C16 | CG | PRO- 202 | 4.23 | 0 | Hydrophobic |
C17 | CD1 | LEU- 204 | 3.97 | 0 | Hydrophobic |
N21 | ZN | ZN- 262 | 1.79 | 0 | Metal Acceptor |