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Atomistry » Calcium » PDB 2g8e-2gsm » 2gsm » |
Calcium in PDB 2gsm: Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter SphaeroidesEnzymatic activity of Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides
All present enzymatic activity of Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides:
1.9.3.1; Protein crystallography data
The structure of Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides, PDB code: 2gsm
was solved by
L.Qin,
C.Hiser,
A.Mulichak,
R.M.Garavito,
S.Ferguson-Miller,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 2gsm:
The structure of Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides
(pdb code 2gsm). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides, PDB code: 2gsm: Jump to Calcium binding site number: 1; 2; Calcium binding site 1 out of 2 in 2gsmGo back to Calcium Binding Sites List in 2gsm
Calcium binding site 1 out
of 2 in the Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides
Mono view Stereo pair view
Calcium binding site 2 out of 2 in 2gsmGo back to Calcium Binding Sites List in 2gsm
Calcium binding site 2 out
of 2 in the Catalytic Core (Subunits I and II) of Cytochrome C Oxidase From Rhodobacter Sphaeroides
Mono view Stereo pair view
Reference:
L.Qin,
C.Hiser,
A.Mulichak,
R.M.Garavito,
S.Ferguson-Miller.
Identification of Conserved Lipid/Detergent-Binding Sites in A High-Resolution Structure of the Membrane Protein Cytochrome C Oxidase. Proc.Natl.Acad.Sci.Usa V. 103 16117 2006.
Page generated: Fri Jul 12 10:54:18 2024
ISSN: ISSN 0027-8424 PubMed: 17050688 DOI: 10.1073/PNAS.0606149103 |
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