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Atomistry » Magnesium » PDB 1nzz-1oev » 1occ » |
Magnesium in PDB 1occ: Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized StateEnzymatic activity of Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State
All present enzymatic activity of Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State:
1.9.3.1; Protein crystallography data
The structure of Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State, PDB code: 1occ
was solved by
T.Tsukihara,
H.Aoyama,
E.Yamashita,
T.Tomizaki,
H.Yamaguchi,
K.Shinzawa-Itoh,
R.Nakashima,
R.Yaono,
S.Yoshikawa,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 1occ:
The structure of Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State
(pdb code 1occ). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State, PDB code: 1occ: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 1occGo back to Magnesium Binding Sites List in 1occ
Magnesium binding site 1 out
of 2 in the Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 1occGo back to Magnesium Binding Sites List in 1occ
Magnesium binding site 2 out
of 2 in the Structure of Bovine Heart Cytochrome C Oxidase at the Fully Oxidized State
Mono view Stereo pair view
Reference:
T.Tsukihara,
H.Aoyama,
E.Yamashita,
T.Tomizaki,
H.Yamaguchi,
K.Shinzawa-Itoh,
R.Nakashima,
R.Yaono,
S.Yoshikawa.
The Whole Structure of the 13-Subunit Oxidized Cytochrome C Oxidase at 2.8 A. Science V. 272 1136 1996.
Page generated: Tue Aug 13 10:36:15 2024
ISSN: ISSN 0036-8075 PubMed: 8638158 |
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