Substrates for peptidase C47.001: staphopain A

Summary Alignment Sequences Sequence features Distribution Structure Literature Substrates

Peptide and protein substrates that are thought to be physiologically relevant are indicated by P. Peptide and protein substrates that are thought to be pathologically relevant are indicated by D. Peptide and protein substrates that are not physiologically relevant are indicated by N. Synthetic substrates are indicated by S. Click on the symbol to show only physiological, non-physiological or synthetic substrates, or here to display all substrates. How cleavage sites have been identified are indicated by the following evidence codes: NT = N-terminal sequencing, MS = mass spectroscopy, MU = mutation, CS = consensus sequence, LC = liquid chromatography. To see all annotated cleavages for a protein substrate, click on the UniProt Accession.

Substrate Uniprot Residue range Cleavage Site Cleavage type Evidence P4 P3 P2 P1 P1' P2' P3' P4' Reference CutDB MERNUM
Abz-Phe-Gly-Ala-Lys-ANB-NH2 Abz-Phe-Gly-Ala-Lys+ANB-NH2 S MS Phe Gly Ala Lys ANB NH2 - - Kalinska et al., 2012
alpha-1-peptidase inhibitor P01009 25-418 peptide-Glu354+Ala-peptide N Met Phe Leu Glu Ala Ile Pro Met Potempa et al., 1986 16358
Bz-Tyr-OEt Bz-Tyr+OEt S - - Z Tyr OEt - - -
MBP-linker-GFP fusion Peptide-Gly+Ala-Peptide N MS Leu Val Leu Gly Ala Met Cpe - Kalinska et al., 2012
Z-Phe-Arg-NHMec Z-Phe-Arg+NHMec S - Z Phe Arg AMC - - -
Z-Phe-Leu-Glu-NHPhNO2 Z-Phe-Leu-Glu+NHPhNO2 S Z Phe Leu Glu NAN - - -