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Atomistry » Magnesium » PDB 5u51-5uhb » 5u99 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 5u51-5uhb » 5u99 » |
Magnesium in PDB 5u99: Transition State Analysis of Adenosine Triphosphate PhosphoribosyltransferaseEnzymatic activity of Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase
All present enzymatic activity of Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase:
2.4.2.17; Protein crystallography data
The structure of Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase, PDB code: 5u99
was solved by
G.-J.Moggre,
M.B.Poulin,
P.C.Tyler,
V.L.Schramm,
E.J.Parker,
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 Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase
(pdb code 5u99). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase, PDB code: 5u99: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 5u99Go back to Magnesium Binding Sites List in 5u99
Magnesium binding site 1 out
of 2 in the Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 5u99Go back to Magnesium Binding Sites List in 5u99
Magnesium binding site 2 out
of 2 in the Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase
Mono view Stereo pair view
Reference:
G.J.Moggre,
M.B.Poulin,
P.C.Tyler,
V.L.Schramm,
E.J.Parker.
Transition State Analysis of Adenosine Triphosphate Phosphoribosyltransferase. Acs Chem. Biol. V. 12 2662 2017.
Page generated: Mon Sep 30 05:14:03 2024
ISSN: ESSN 1554-8937 PubMed: 28872824 DOI: 10.1021/ACSCHEMBIO.7B00484 |
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