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Atomistry » Iron » PDB 4l0d-4lji » 4l2b » |
Iron in PDB 4l2b: X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas HaloplanktisEnzymatic activity of X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis
All present enzymatic activity of X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis:
1.15.1.1; Protein crystallography data
The structure of X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis, PDB code: 4l2b
was solved by
A.Merlino,
I.Russo Krauss,
F.Sica,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Iron Binding Sites:
The binding sites of Iron atom in the X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis
(pdb code 4l2b). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis, PDB code: 4l2b: Jump to Iron binding site number: 1; 2; Iron binding site 1 out of 2 in 4l2bGo back to Iron Binding Sites List in 4l2b
Iron binding site 1 out
of 2 in the X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis
Mono view Stereo pair view
Iron binding site 2 out of 2 in 4l2bGo back to Iron Binding Sites List in 4l2b
Iron binding site 2 out
of 2 in the X-Ray Structure of the C57S Mutant of the Iron Superoxide Dismutase From Pseudoalteromonas Haloplanktis
Mono view Stereo pair view
Reference:
A.Merlino,
I.Russo Krauss,
I.Castellano,
M.R.Ruocco,
A.Capasso,
E.De Vendittis,
B.Rossi,
F.Sica.
Structural and Denaturation Studies of Two Mutants of A Cold Adapted Superoxide Dismutase Point to the Importance of Electrostatic Interactions in Protein Stability. Biochim.Biophys.Acta V.1844 632 2014.
Page generated: Mon Aug 5 06:02:38 2024
ISSN: ISSN 0006-3002 PubMed: 24440460 DOI: 10.1016/J.BBAPAP.2014.01.007 |
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