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Atomistry » Magnesium » PDB 3twp-3u89 » 3u7q | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 3twp-3u89 » 3u7q » |
Magnesium in PDB 3u7q: A. Vinelandii Nitrogenase Mofe Protein at Atomic ResolutionEnzymatic activity of A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution
All present enzymatic activity of A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution:
1.18.6.1; Protein crystallography data
The structure of A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution, PDB code: 3u7q
was solved by
T.Spatzal,
O.Einsle,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 3u7q:
The structure of A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution
(pdb code 3u7q). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution, PDB code: 3u7q: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 3u7qGo back to Magnesium Binding Sites List in 3u7q
Magnesium binding site 1 out
of 2 in the A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 3u7qGo back to Magnesium Binding Sites List in 3u7q
Magnesium binding site 2 out
of 2 in the A. Vinelandii Nitrogenase Mofe Protein at Atomic Resolution
Mono view Stereo pair view
Reference:
T.Spatzal,
M.Aksoyoglu,
L.Zhang,
S.L.Andrade,
E.Schleicher,
S.Weber,
D.C.Rees,
O.Einsle.
Evidence For Interstitial Carbon in Nitrogenase Femo Cofactor. Science V. 334 940 2011.
Page generated: Thu Aug 15 12:25:20 2024
ISSN: ISSN 0036-8075 PubMed: 22096190 DOI: 10.1126/SCIENCE.1214025 |
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