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Crystal Structure of SIRT3 in complex with H4K16bhb peptide[HYDROLASE]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Crystal Structure of SIRT3 in complex with H3K4bhb peptide[HYDROLASE]
Crystal Structure of SIRT3 in complex with H3K9bhb peptide[HYDROLASE]
Human SIRT3 Recognizing H3K4cr[HYDROLASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Human SIRT3 in complex with halistanol sulfate[HYDROLASE/INHIBITOR]
Crystal structure of SIRT3 bound to a leucylated AceCS2[HYDROLASE]
Crystal structure of hSIRT3 in complex with a specific agonist Amiodarone hydrochloride[HYDROLASE]
Crystal structure of human Sirt3 at an improved resolution[HYDROLASE]
Crystal structure of human SIRT3 in complex with compound (2-butylbenzofuran-3-yl)(4-(2-(diethylamino)ethoxy)-3,5-diiodophenyl)methanone[HYDROLASE]
Complex of human Sirt3 with Bromo-Resveratrol and Fluor-De-Lys peptide[HYDROLASE/PEPTIDE]
Complex of human Sirt3 with Bromo-Resveratrol and ACS2 peptide[HYDROLASE]
CRYSTAL STRUCTURE OF HUMAN SIRT3 IN COMPLEX WITH THE INHIBITOR EX-527 AND 2'-O-ACETYL-ADP-RIBOSE[HYDROLASE]
CRYSTAL STRUCTURE OF HUMAN SIRT3 IN COMPLEX WITH NATIVE ALKYLIMIDATE FORMED FROM ACETYL-LYSINE ACS2-PEPTIDE CRYSTALLIZED IN PRESENCE OF THE INHIBITOR EX-527[HYDROLASE/LIGASE]
CRYSTAL STRUCTURE OF HUMAN SIRT3 IN COMPLEX WITH THIOALKYLIMIDATE FORMED FROM THIO-ACETYL-LYSINE ACS2-PEPTIDE CRYSTALLIZED IN PRESENCE OF THE INHIBITOR EX-527[HYDROLASE/LIGASE]
CRYSTAL STRUCTURE OF HUMAN SIRT3 IN COMPLEX WITH THIOALKYLIMIDATE FORMED FROM THIO-ACETYL-LYSINE ACS2-PEPTIDE[HYDROLASE/LIGASE]
CRYSTAL STRUCTURE OF HUMAN SIRT3 IN COMPLEX WITH THE INHIBITOR EX-527 AND ADP-RIBOSE[HYDROLASE]
CRYSTAL STRUCTURE OF SIRT3 IN COMPLEX WITH THE INHIBITOR EX-527 AND NAD[HYDROLASE]
Structure of human SIRT3 in complex with SRT1720 inhibitor[HYDROLASE]
Crystal Structure of human SIRT3 with ELT inhibitor 3 [14-(4-{2-[(methylsulfonyl)amino]ethyl}piperidin-1-yl)thieno[3,2-d]pyrimidine-6-carboxamide][HYDROLASE/HYDROLASE INHIBITOR]
Crystal Structure of human SIRT3 with ELT inhibitor 28 [4-(4-{2-[(2,2-dimethylpropanoyl)amino]ethyl}piperidin-1-yl)thieno[3,2-d]pyrimidine-6-carboxamide[[HYDROLASE/HYDROLASE INHIBITOR]
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