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Atomistry » Calcium » PDB 3bje-3bxk » 3bxi » |
Calcium in PDB 3bxi: Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A ResolutionEnzymatic activity of Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution
All present enzymatic activity of Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution:
1.11.1.7; Protein crystallography data
The structure of Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution, PDB code: 3bxi
was solved by
A.K.Singh,
N.Singh,
S.Sharma,
K.Shin,
M.Takase,
P.Kaur,
A.Srinivasan,
T.P.Singh,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 3bxi:
The structure of Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution
(pdb code 3bxi). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution, PDB code: 3bxi: Calcium binding site 1 out of 1 in 3bxiGo back to Calcium Binding Sites List in 3bxi
Calcium binding site 1 out
of 1 in the Structure of the Complex of Bovine Lactoperoxidase with Its Catalyzed Product Hypothiocyanate Ion at 2.3A Resolution
Mono view Stereo pair view
Reference:
A.K.Singh,
N.Singh,
S.Sharma,
K.Shin,
M.Takase,
P.Kaur,
A.Srinivasan,
T.P.Singh.
Inhibition of Lactoperoxidase By Its Own Catalytic Product: Crystal Structure of the Hypothiocyanate-Inhibited Bovine Lactoperoxidase at 2.3-A Resolution. Biophys.J. V. 96 646 2009.
Page generated: Sat Jul 13 08:27:35 2024
ISSN: ISSN 0006-3495 PubMed: 19167310 DOI: 10.1016/J.BPJ.2008.09.019 |
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