Substrates for peptidase S24.001: repressor LexA

Summary Alignment Tree 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
lexA repressor P0A274 1-202 peptide-Ala84+Gly-peptide N Arg Val Ala Ala Gly Glu Pro Leu
lexA repressor P0A273 1-202 peptide-Ala84+Gly-peptide N Arg Val Ala Ala Gly Glu Pro Leu Little, 1993 17723
repressor LexA P0A7C2 1-202 peptide-Ala84+Gly-peptide P Arg Val Ala Ala Gly Glu Pro Leu Little, 2004
repressor LexA P31080 1-205 peptide-Ala91+Gly-peptide N Lys Val Thr Ala Gly Ser Pro Ile 17722