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Literature summary for 3.4.13.20 extracted from

  • Cacciatore, I.; Cocco, A.; Costa, M.; Fontana, M.; Lucente, G.; Pecci, L.; Pinnen, F.
    Biochemical properties of new synthetic carnosine analogues containing the residue of 2,3-diaminopropionic acid: the effect of N-acetylation (2005), Amino Acids, 28, 77-83.
    View publication on PubMed
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Inhibitors

Inhibitors Comment Organism Structure
3-(acetylamino)-L-alanyl-L-histidine 2.3 mM, 50% inhibition of 3-nitrotyrosine formation Homo sapiens
3-amino-L-alanyl-L-histidine 3.3 mM, 50% inhibition of 3-nitrotyrosine formation Homo sapiens
N-acetyl-3-(acetylamino)-L-alanyl-L-histidine 2.5 mM, 50% inhibition of 3-nitrotyrosine formation Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
blood serum
-
 Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3-(acetylamino)-L-alanyl-L-histidine + H2O 3% of the activity with carnosine Homo sapiens 3-(acetylamino)-L-alanine + L-histidine
-
 ?
3-amino-L-alanyl-L-histidine + H2O 30% of the activity with carnosine Homo sapiens 3-amino-L-alanine + L-histidine
-
 ?
beta-Ala-His + H2O i.e. carnosine Homo sapiens beta-Ala + His
-
 ?
N-acetyl-3-(acetylamino)-L-alanyl-L-histidine + H2O 63% of the activity with carnosine Homo sapiens N-acetyl-3-(acetylamino)-L-alanine + L-histidine
-
 ?