Substrates for peptidase S21.004: herpesvirus 6-type assemblin

Summary Alignment Sequences Sequence features Distribution Literature Substrates Pharma

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
herpesvirus 6-type assemblin P24433 1-528 peptide-Ala230+Ser-peptide P Tyr Ile Lys Ala Ser Glu Pro Pro Tigue & Kay, 1998 17716
herpesvirus 6-type assemblin P24433 1-528 peptide-Ala491+Ser-peptide P Ile Leu Asn Ala Ser Leu Ala Pro Tigue & Kay, 1998 17717
Suc-Arg-Arg-Ile-Leu-Asn-Ala-Ser-Leu-Ala-Pro-Glu-NH2 Suc-Arg-Arg-Ile-Leu-Asn-Ala+Ser-Leu-Ala-Pro-Glu-NH2 S Ile Leu Asn Ala Ser Leu Ala Pro Tigue & Kay, 2004
Suc-Arg-Arg-Tyr-Ile-Lys-Ala-Ser-Glu-Pro-Pro-Val-NH2 Suc-Arg-Arg-Tyr-Ile-Lys-Ala+Ser-Glu-Pro-Pro-Val-NH2 S Tyr Ile Lys Ala Ser Glu Pro Pro Tigue & Kay, 2004