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Atomistry » Magnesium » PDB 3rer-3rqx » 3rqh » |
Magnesium in PDB 3rqh: Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') HexaphosphateEnzymatic activity of Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') Hexaphosphate
All present enzymatic activity of Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') Hexaphosphate:
4.2.1.93; Protein crystallography data
The structure of Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') Hexaphosphate, PDB code: 3rqh
was solved by
I.A.Shumilin,
M.Cymborowski,
A.Joachimiak,
W.Minor,
Midwest Center Forstructural Genomics (Mcsg),
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') Hexaphosphate
(pdb code 3rqh). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') Hexaphosphate, PDB code: 3rqh: Magnesium binding site 1 out of 1 in 3rqhGo back to Magnesium Binding Sites List in 3rqh
Magnesium binding site 1 out
of 1 in the Crystal Structure of Adp/Atp-Dependent Nad(P)H-Hydrate Dehydratase From Bacillus Subtilis in Complex with P1,P6-Di(Adenosine-5') Hexaphosphate
Mono view Stereo pair view
Reference:
I.A.Shumilin,
M.Cymborowski,
O.Chertihin,
K.N.Jha,
J.C.Herr,
S.A.Lesley,
A.Joachimiak,
W.Minor.
Identification of Unknown Protein Function Using Metabolite Cocktail Screening. Structure V. 20 1715 2012.
Page generated: Thu Aug 15 10:34:18 2024
ISSN: ISSN 0969-2126 PubMed: 22940582 DOI: 10.1016/J.STR.2012.07.016 |
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