Substrates for peptidase C03.016: tomato marchitez virus 3C peptidase

Summary Alignment Sequences Sequence features Distribution 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
polyprotein A0A140G942 1-1189 peptide-Gln466+Ala-peptide P NT Arg Gln Ala Gln Ala Lys Ser Thr Ferriol et al., 2016
polyprotein A0A140G942 1-1189 peptide-Gln720+Ala-peptide P NT Met Ile Ala Gln Ala Gln Tyr Gly Ferriol et al., 2016
polyprotein A0A140G942 1-1189 peptide-Gln964+Ser-peptide P NT Lys Arg Gly Gln Ser Ile Leu Thr Ferriol et al., 2016
polyprotein C7EXM4 1-1197 peptide-Gln474+Val-peptide P NT Lys Leu Ala Gln Val Ala Gly Ala Ferriol et al., 2016
polyprotein C7EXM4 1-1197 peptide-Gln728+Ser-peptide P NT Leu Ile Ala Gln Ser Gln Phe Gly Ferriol et al., 2016
polyprotein C7EXM4 1-1197 peptide-Gln972+Val-peptide P NT Lys Gln Ser Gln Val Asn Leu Ser Ferriol et al., 2016