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Atomistry » Magnesium » PDB 5oea-5onv » 5oi5 » |
Magnesium in PDB 5oi5: Dissociation of Biochemical and Antiretroviral Activities of Integrase-Ledgf Allosteric Inhibitors Revealed By Resistance of A125 Polymorphic Hiv-1Protein crystallography data
The structure of Dissociation of Biochemical and Antiretroviral Activities of Integrase-Ledgf Allosteric Inhibitors Revealed By Resistance of A125 Polymorphic Hiv-1, PDB code: 5oi5
was solved by
M.Ruff,
R.Benarous,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5oi5:
The structure of Dissociation of Biochemical and Antiretroviral Activities of Integrase-Ledgf Allosteric Inhibitors Revealed By Resistance of A125 Polymorphic Hiv-1 also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Dissociation of Biochemical and Antiretroviral Activities of Integrase-Ledgf Allosteric Inhibitors Revealed By Resistance of A125 Polymorphic Hiv-1
(pdb code 5oi5). 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 Dissociation of Biochemical and Antiretroviral Activities of Integrase-Ledgf Allosteric Inhibitors Revealed By Resistance of A125 Polymorphic Hiv-1, PDB code: 5oi5: Magnesium binding site 1 out of 1 in 5oi5Go back to![]() ![]()
Magnesium binding site 1 out
of 1 in the Dissociation of Biochemical and Antiretroviral Activities of Integrase-Ledgf Allosteric Inhibitors Revealed By Resistance of A125 Polymorphic Hiv-1
![]() Mono view ![]() Stereo pair view
Reference:
D.Bonnard,
E.Le Rouzic,
S.Eiler,
C.Amadori,
I.Orlov,
J.M.Bruneau,
J.Brias,
J.Barbion,
F.Chevreuil,
D.Spehner,
S.Chasset,
B.Ledoussal,
F.Moreau,
A.Saib,
B.P.Klaholz,
S.Emiliani,
M.Ruff,
A.Zamborlini,
R.Benarous.
Structure-Function Analyses Unravel Distinct Effects of Allosteric Inhibitors of Hiv-1 Integrase on Viral Maturation and Integration. J. Biol. Chem. V. 293 6172 2018.
Page generated: Tue Aug 12 17:33:20 2025
ISSN: ESSN 1083-351X PubMed: 29507092 DOI: 10.1074/JBC.M117.816793 |
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