Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
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Click Chemistry Reagent for Identification of Sites of Covalent Ligand Incorporation in Integral Membrane Proteins.Shedding Light on Anesthetic Mechanisms: Application of Photoaffinity Ligands.Thienopyrimidinone Based Sirtuin-2 (SIRT2)-Selective Inhibitors Bind in the Ligand Induced Selectivity Pocket.Recent progress on the molecular pharmacology of propofol.
P2860
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
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2015 nî lūn-bûn
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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի փետրվարին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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name
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@ast
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@en
type
label
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@ast
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@en
prefLabel
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@ast
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@en
P2860
P356
P1476
Propofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.
@en
P2093
Brian P Weiser
Roderic G Eckenhoff
P2860
P304
P356
10.1074/JBC.M114.620732
P407
P577
2015-02-09T00:00:00Z