Substrates for peptidase S69.001: Tellina virus 1 VP4 peptidase

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	P4	P3	P2	P1	P1'	P2'	P3'	P4'	Reference
polyprotein	Q2PBR5	1-1114	peptide-Ala830+Ser-peptide	P	Val	Ala	Gln	Ala	Ser	Thr	Asn	Pro	Nobiron et al., 2008
polyprotein	Q2PBR5	1-1114	peptide-Ala618+Ala-peptide	P	Val	Ala	Gln	Ala	Ala	Asp	Arg	Pro	Nobiron et al., 2008
polyprotein	Q2PBR5	1-1114	peptide-Ala451+Trp-peptide	P	Leu	Ala	Met	Ala	Trp	Glu	Trp	Ser	Nobiron et al., 2008
polyprotein	Q2PBR5	1-1114	peptide-Ala512+Gly-peptide	P	Met	Ala	Leu	Ala	Gly	Glu	Arg	Pro	Nobiron et al., 2008
polyprotein	Q2PBR5	1-1114	peptide-Ala492+Ala-peptide	P	Met	Ala	Asn	Ala	Ala	Ser	Gly	Arg	Nobiron et al., 2008
polyprotein	Q2PBR5	1-1114	peptide-Ala499+Ala-peptide	P	Arg	Ala	Leu	Ala	Ala	Ser	Gly	Lys	Nobiron et al., 2008