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Atomistry » Zinc » PDB 1nvf-1oi0 » 1ocr | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Zinc » PDB 1nvf-1oi0 » 1ocr » |
Zinc in PDB 1ocr: Bovine Heart Cytochrome C Oxidase in the Fully Reduced StateEnzymatic activity of Bovine Heart Cytochrome C Oxidase in the Fully Reduced State
All present enzymatic activity of Bovine Heart Cytochrome C Oxidase in the Fully Reduced State:
1.9.3.1; Protein crystallography data
The structure of Bovine Heart Cytochrome C Oxidase in the Fully Reduced State, PDB code: 1ocr
was solved by
T.Tsukihara,
M.Yao,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 1ocr:
The structure of Bovine Heart Cytochrome C Oxidase in the Fully Reduced State also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Bovine Heart Cytochrome C Oxidase in the Fully Reduced State
(pdb code 1ocr). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Bovine Heart Cytochrome C Oxidase in the Fully Reduced State, PDB code: 1ocr: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 1ocrGo back to![]() ![]()
Zinc binding site 1 out
of 2 in the Bovine Heart Cytochrome C Oxidase in the Fully Reduced State
![]() Mono view ![]() Stereo pair view
Zinc binding site 2 out of 2 in 1ocrGo back to![]() ![]()
Zinc binding site 2 out
of 2 in the Bovine Heart Cytochrome C Oxidase in the Fully Reduced State
![]() Mono view ![]() Stereo pair view
Reference:
S.Yoshikawa,
K.Shinzawa-Itoh,
R.Nakashima,
R.Yaono,
E.Yamashita,
N.Inoue,
M.Yao,
M.J.Fei,
C.P.Libeu,
T.Mizushima,
H.Yamaguchi,
T.Tomizaki,
T.Tsukihara.
Redox-Coupled Crystal Structural Changes in Bovine Heart Cytochrome C Oxidase. Science V. 280 1723 1998.
Page generated: Wed Oct 16 17:29:09 2024
ISSN: ISSN 0036-8075 PubMed: 9624044 DOI: 10.1126/SCIENCE.280.5370.1723 |
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