Atomistry » Zinc » PDB 6rg4-6rpc » 6rl9
Atomistry »
  Zinc »
    PDB 6rg4-6rpc »
      6rl9 »

Zinc in PDB 6rl9: Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide

Enzymatic activity of Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide

All present enzymatic activity of Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide:
4.2.1.1;

Protein crystallography data

The structure of Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide, PDB code: 6rl9 was solved by S.Gloeckner, A.Heine, G.Klebe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 32.02 / 1.00
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 42.431, 41.387, 72.304, 90.00, 104.71, 90.00
R / Rfree (%) 11.9 / 13

Other elements in 6rl9:

The structure of Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide also contains other interesting chemical elements:

Mercury (Hg) 3 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide (pdb code 6rl9). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide, PDB code: 6rl9:

Zinc binding site 1 out of 1 in 6rl9

Go back to Zinc Binding Sites List in 6rl9
Zinc binding site 1 out of 1 in the Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Human Carbonic Anhydrase II in Complex with 4-Aminobenzenesulfonamide within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn301

b:5.5
occ:1.00
 N2 A:SAN304 1.9 5.7 1.0
NE2 A:HIS94 2.0 5.6 1.0
ND1 A:HIS119 2.0 5.3 1.0
NE2 A:HIS96 2.0 5.7 1.0
CE1 A:HIS119 2.9 5.5 1.0
O2 A:SAN304 3.0 7.0 1.0
CD2 A:HIS96 3.0 5.8 1.0
CE1 A:HIS94 3.0 6.0 1.0
CD2 A:HIS94 3.0 5.8 1.0
S A:SAN304 3.0 6.4 1.0
CE1 A:HIS96 3.0 6.5 1.0
HE1 A:HIS119 3.1 6.6 1.0
CG A:HIS119 3.1 5.6 1.0
HD2 A:HIS96 3.2 7.0 1.0
HB2 A:HIS119 3.2 6.7 1.0
HD2 A:HIS94 3.2 7.0 1.0
HE1 A:HIS94 3.2 7.2 1.0
HE1 A:HIS96 3.2 7.8 1.0
CB A:HIS119 3.6 5.6 1.0
HG1 A:THR199 3.6 7.0 1.0
O A:HOH553 3.7 11.5 1.0
HB3 A:HIS119 3.7 6.7 1.0
OG1 A:THR199 3.8 5.8 1.0
OE1 A:GLU106 4.0 6.0 1.0
O1 A:SAN304 4.1 6.7 1.0
NE2 A:HIS119 4.1 5.8 1.0
ND1 A:HIS94 4.1 5.8 1.0
ND1 A:HIS96 4.1 7.3 1.0
CG A:HIS94 4.2 5.8 1.0
CG A:HIS96 4.2 6.2 1.0
CD2 A:HIS119 4.2 5.7 1.0
C4 A:SAN304 4.2 7.6 1.0
HH2 A:TRP209 4.2 8.1 1.0
HE2 A:HIS119 4.9 6.9 1.0
HG23 A:THR200 4.9 11.4 1.0
C5 A:SAN304 4.9 8.4 1.0
O A:HOH516 4.9 17.6 1.0
HD1 A:HIS94 4.9 7.0 1.0
HD1 A:HIS96 4.9 8.8 1.0
HG11 A:VAL143 4.9 8.3 1.0
CD A:GLU106 4.9 6.2 1.0
C3 A:SAN304 5.0 8.2 1.0

Reference:

S.Glockner, K.Ngo, B.Wagner, A.Heine, G.Klebe. The Influence of Varying Fluorination Patterns on the Thermodynamics and Kinetics of Benzenesulfonamide Binding to Human Carbonic Anhydrase II. Biomolecules V. 10 2020.
ISSN: ESSN 2218-273X
PubMed: 32230853
DOI: 10.3390/BIOM10040509
Page generated: Tue Oct 29 06:38:08 2024

Last articles

As in 1IHU
As in 1I83
As in 1I9T
As in 1I9S
As in 1HYV
As in 1I19
As in 1GLJ
As in 1GQ8
As in 1GR0
As in 1FU1
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy