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Atomistry » Iron » PDB 2xv1-2yde » 2y8h | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Iron » PDB 2xv1-2yde » 2y8h » |
Iron in PDB 2y8h: Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis DossProtein crystallography data
The structure of Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis Doss, PDB code: 2y8h
was solved by
H.Y.Cho,
H.J.Cho,
B.S.Kang,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 2y8h:
The structure of Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis Doss also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis Doss
(pdb code 2y8h). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis Doss, PDB code: 2y8h: Jump to Iron binding site number: 1; 2; Iron binding site 1 out of 2 in 2y8hGo back to Iron Binding Sites List in 2y8h
Iron binding site 1 out
of 2 in the Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis Doss
Mono view Stereo pair view
Iron binding site 2 out of 2 in 2y8hGo back to Iron Binding Sites List in 2y8h
Iron binding site 2 out
of 2 in the Structure of the First Gaf Domain E87G Mutant of Mycobacterium Tuberculosis Doss
Mono view Stereo pair view
Reference:
H.Y.Cho,
H.J.Cho,
M.H.Kim,
B.S.Kang.
Blockage of the Channel to Heme By the E87 Side Chain in the Gaf Domain of Mycobacterium Tuberculosis Doss Confers the Unique Sensitivity of Doss to Oxygen. Febs Lett. V. 585 1873 2011.
Page generated: Sun Aug 4 05:09:24 2024
ISSN: ISSN 0014-5793 PubMed: 21536032 DOI: 10.1016/J.FEBSLET.2011.04.050 |
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