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Literature summary for 2.3.1.B41 extracted from

  • Liu, J.; Zheng, W.
    Cyclic peptide-based potent human SIRT6 inhibitors (2016), Org. Biomol. Chem., 14, 5928-5935.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
H2N-AK-(N(epsilon)-thioacetyl-)lysine-LM-COOH moderate potent inhibitor Homo sapiens
H2N-HK-(N(epsilon)-thioacetyl-)lysine-LM-COOH moderate potent inhibitor Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
NAD+ + [histone H3]-N6-acetyl-L-lysine9 Homo sapiens
-
nicotinamide + [histone H3]-L-lysine + 2'-O-acetyl-ADP ribose
-
?

Organism

Organism UniProt Comment Textmining
Homo sapiens Q8N6T7
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
NAD+ + [histone H3]-N6-acetyl-L-lysine9
-
Homo sapiens nicotinamide + [histone H3]-L-lysine + 2'-O-acetyl-ADP ribose
-
?

Synonyms

Synonyms Comment Organism
SIRT6
-
Homo sapiens

Cofactor

Cofactor Comment Organism Structure
NAD+ dependent on Homo sapiens