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Atomistry » Fluorine » PDB 6qy8-6rkn » 6rkn » |
Fluorine in PDB 6rkn: Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.Enzymatic activity of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.
All present enzymatic activity of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.:
4.2.1.1; Protein crystallography data
The structure of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide., PDB code: 6rkn
was solved by
S.Gloeckner,
A.Heine,
G.Klebe,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 6rkn:
The structure of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide. also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.
(pdb code 6rkn). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 2 binding sites of Fluorine where determined in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide., PDB code: 6rkn: Jump to Fluorine binding site number: 1; 2; Fluorine binding site 1 out of 2 in 6rknGo back to Fluorine Binding Sites List in 6rkn
Fluorine binding site 1 out
of 2 in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.
Mono view Stereo pair view
Fluorine binding site 2 out of 2 in 6rknGo back to Fluorine Binding Sites List in 6rkn
Fluorine binding site 2 out
of 2 in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.
Mono view Stereo pair view
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.
Page generated: Fri Aug 2 01:15:20 2024
ISSN: ESSN 2218-273X PubMed: 32230853 DOI: 10.3390/BIOM10040509 |
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