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Atomistry » Molybdenum » PDB 2ca3-3fah » 2nya » |
Molybdenum in PDB 2nya: Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia ColiEnzymatic activity of Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli
All present enzymatic activity of Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli:
1.7.99.4; Protein crystallography data
The structure of Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli, PDB code: 2nya
was solved by
B.J.N.Jepson,
D.J.Richardson,
A.M.Hemmings,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 2nya:
The structure of Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli also contains other interesting chemical elements:
Molybdenum Binding Sites:
The binding sites of Molybdenum atom in the Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli
(pdb code 2nya). This binding sites where shown within
5.0 Angstroms radius around Molybdenum atom.
In total 2 binding sites of Molybdenum where determined in the Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli, PDB code: 2nya: Jump to Molybdenum binding site number: 1; 2; Molybdenum binding site 1 out of 2 in 2nyaGo back to Molybdenum Binding Sites List in 2nya
Molybdenum binding site 1 out
of 2 in the Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli
Mono view Stereo pair view
Molybdenum binding site 2 out of 2 in 2nyaGo back to Molybdenum Binding Sites List in 2nya
Molybdenum binding site 2 out
of 2 in the Crystal Structure of the Periplasmic Nitrate Reductase (Nap) From Escherichia Coli
Mono view Stereo pair view
Reference:
B.J.Jepson,
S.Mohan,
T.A.Clarke,
A.J.Gates,
J.A.Cole,
C.S.Butler,
J.N.Butt,
A.M.Hemmings,
D.J.Richardson.
Spectropotentiometric and Structural Analysis of the Periplasmic Nitrate Reductase From Escherichia Coli J.Biol.Chem. V. 282 6425 2007.
Page generated: Sun Oct 6 15:47:16 2024
ISSN: ISSN 0021-9258 PubMed: 17130127 DOI: 10.1074/JBC.M607353200 |
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