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Atomistry » Zinc » PDB 7aof-7av1 » 7aq2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Zinc » PDB 7aof-7av1 » 7aq2 » |
Zinc in PDB 7aq2: Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583AEnzymatic activity of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A
All present enzymatic activity of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A:
1.7.2.4; Protein crystallography data
The structure of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A, PDB code: 7aq2
was solved by
L.Zhang,
E.Bill,
P.M.H.Kroneck,
O.Einsle,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 7aq2:
The structure of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A
(pdb code 7aq2). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A, PDB code: 7aq2: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 7aq2Go back to![]() ![]()
Zinc binding site 1 out
of 2 in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A
![]() Mono view ![]() Stereo pair view
Zinc binding site 2 out of 2 in 7aq2Go back to![]() ![]()
Zinc binding site 2 out
of 2 in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583A
![]() Mono view ![]() Stereo pair view
Reference:
L.Zhang,
E.Bill,
P.M.H.Kroneck,
O.Einsle.
Histidine-Gated Proton-Coupled Electron Transfer to the Cu A Site of Nitrous Oxide Reductase. J.Am.Chem.Soc. 2020.
Page generated: Tue Oct 29 17:07:13 2024
ISSN: ESSN 1520-5126 PubMed: 33377777 DOI: 10.1021/JACS.0C10057 |
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