Substrates for peptidase S08.149: CDF peptidase

Summary Alignment Tree 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
insulin P01308 25-54 peptide-Phe48+Phe-peptide N Glu Arg Gly Phe Phe Tyr Thr Pro Cheng et al., 2009
insulin P01308 25-54 peptide-Leu35+Val-peptide N Gly Ser His Leu Val Glu Ala Leu Cheng et al., 2009
insulin P01308 25-54 peptide-Leu39+Tyr-peptide N Val Glu Ala Leu Tyr Leu Val Cys Cheng et al., 2009
serine protease A1E5M0 1-377 peptide-Thr85+Ile-peptide P NT Ile Arg Ile Thr Ile Thr Glu Pro Cheng et al., 2009
serine protease A1E5M0 86-377 peptide-Leu94+Asn-peptide P NT Val Gly Thr Leu Asn Thr Pro Val Cheng et al., 2009