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Chlorine in PDB 8qn0: Soluble Epoxide Hydrolase in Complex with RK3Enzymatic activity of Soluble Epoxide Hydrolase in Complex with RK3
All present enzymatic activity of Soluble Epoxide Hydrolase in Complex with RK3:
3.1.3.76; 3.3.2.10; Protein crystallography data
The structure of Soluble Epoxide Hydrolase in Complex with RK3, PDB code: 8qn0
was solved by
A.Kumar,
F.Zhu,
J.M.H.Ehrler,
F.Li,
C.Empel,
Y.Xu,
I.Atodiresei,
R.M.Koenigs,
E.Proschak,
S.Knapp,
Structural Genomics Consortium (Sgc),
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Soluble Epoxide Hydrolase in Complex with RK3
(pdb code 8qn0). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the Soluble Epoxide Hydrolase in Complex with RK3, PDB code: 8qn0: Jump to Chlorine binding site number: 1; 2; 3; 4; Chlorine binding site 1 out of 4 in 8qn0Go back to Chlorine Binding Sites List in 8qn0
Chlorine binding site 1 out
of 4 in the Soluble Epoxide Hydrolase in Complex with RK3
Mono view Stereo pair view
Chlorine binding site 2 out of 4 in 8qn0Go back to Chlorine Binding Sites List in 8qn0
Chlorine binding site 2 out
of 4 in the Soluble Epoxide Hydrolase in Complex with RK3
Mono view Stereo pair view
Chlorine binding site 3 out of 4 in 8qn0Go back to Chlorine Binding Sites List in 8qn0
Chlorine binding site 3 out
of 4 in the Soluble Epoxide Hydrolase in Complex with RK3
Mono view Stereo pair view
Chlorine binding site 4 out of 4 in 8qn0Go back to Chlorine Binding Sites List in 8qn0
Chlorine binding site 4 out
of 4 in the Soluble Epoxide Hydrolase in Complex with RK3
Mono view Stereo pair view
Reference:
F.Li,
W.F.Zhu,
C.Empel,
O.Datsenko,
A.Kumar,
Y.Xu,
J.H.M.Ehrler,
I.Atodiresei,
S.Knapp,
P.K.Mykhailiuk,
E.Proschak,
R.M.Koenigs.
Photosensitization Enables Pauson-Khand-Type Reactions with Nitrenes. Science V. 383 498 2024.
Page generated: Tue Jul 30 12:01:57 2024
ISSN: ESSN 1095-9203 PubMed: 38301027 DOI: 10.1126/SCIENCE.ADM8095 |
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