2.000 Å
X-ray
2001-04-12
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: | 10.932 |
---|---|
Number of residues: | 22 |
Including | |
Standard Amino Acids: | 21 |
Non Standard Amino Acids: | 1 |
Water Molecules: | 0 |
Cofactors: | |
Metals: | ZN |
Ligandability | Volume (Å3) |
---|---|
0.704 | 388.125 |
% Hydrophobic | % Polar |
---|---|
50.43 | 49.57 |
According to VolSite |
HET Code: | FBT |
---|---|
Formula: | C6H5F2NO2S |
Molecular weight: | 193.171 g/mol |
DrugBank ID: | DB03270 |
Buried Surface Area: | 64.16 % |
Polar Surface area: | 68.54 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 2 |
H-Bond Donors: | 1 |
Rings: | 1 |
Aromatic rings: | 1 |
Anionic atoms: | 0 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 1 |
X | Y | Z |
---|---|---|
-5.47892 | 2.14983 | 15.9903 |
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 |
C05 | CG2 | VAL- 121 | 3.84 | 0 | Hydrophobic |
C06 | CG1 | VAL- 121 | 4.22 | 0 | Hydrophobic |
F12 | CG1 | VAL- 121 | 3.42 | 0 | Hydrophobic |
F12 | CG2 | VAL- 143 | 4.01 | 0 | Hydrophobic |
F11 | CB | LEU- 198 | 4.18 | 0 | Hydrophobic |
C01 | CD2 | LEU- 198 | 4.31 | 0 | Hydrophobic |
O08 | N | THR- 199 | 2.91 | 162.35 | H-Bond (Protein Donor) |
NP0 | OG1 | THR- 199 | 3.05 | 175.28 | H-Bond (Ligand Donor) |
F11 | CG2 | THR- 200 | 3.21 | 0 | Hydrophobic |
NP0 | ZN | ZN- 262 | 1.79 | 0 | Metal Acceptor |