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Atomistry » Magnesium » PDB 3ump-3v4f » 3uqy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 3ump-3v4f » 3uqy » |
Magnesium in PDB 3uqy: H2-Reduced Structure of E. Coli Hydrogenase-1Enzymatic activity of H2-Reduced Structure of E. Coli Hydrogenase-1
All present enzymatic activity of H2-Reduced Structure of E. Coli Hydrogenase-1:
1.12.99.6; Protein crystallography data
The structure of H2-Reduced Structure of E. Coli Hydrogenase-1, PDB code: 3uqy
was solved by
A.Volbeda,
J.C.Fontecilla-Camps,
C.Darnault,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 3uqy:
The structure of H2-Reduced Structure of E. Coli Hydrogenase-1 also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the H2-Reduced Structure of E. Coli Hydrogenase-1
(pdb code 3uqy). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the H2-Reduced Structure of E. Coli Hydrogenase-1, PDB code: 3uqy: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 3uqyGo back to Magnesium Binding Sites List in 3uqy
Magnesium binding site 1 out
of 2 in the H2-Reduced Structure of E. Coli Hydrogenase-1
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 3uqyGo back to Magnesium Binding Sites List in 3uqy
Magnesium binding site 2 out
of 2 in the H2-Reduced Structure of E. Coli Hydrogenase-1
Mono view Stereo pair view
Reference:
A.Volbeda,
P.Amara,
C.Darnault,
J.M.Mouesca,
A.Parkin,
M.M.Roessler,
F.A.Armstrong,
J.C.Fontecilla-Camps.
X-Ray Crystallographic and Computational Studies of the O2-Tolerant [Nife]-Hydrogenase 1 From Escherichia Coli. Proc.Natl.Acad.Sci.Usa V. 109 5305 2012.
Page generated: Thu Aug 15 12:38:09 2024
ISSN: ISSN 0027-8424 PubMed: 22431599 DOI: 10.1073/PNAS.1119806109 |
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