COGC_PARCM
ID COGC_PARCM Reviewed; 20 AA.
AC P20734;
DT 01-FEB-1991, integrated into UniProtKB/Swiss-Prot.
DT 01-FEB-1991, sequence version 1.
DT 03-AUG-2022, entry version 65.
DE RecName: Full=Collagenolytic protease 36 kDa C;
DE EC=3.4.21.32;
DE Flags: Fragment;
OS Paralithodes camtschaticus (Red king crab).
OC Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea;
OC Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Anomura;
OC Paguroidea; Lithodidae; Paralithodes.
OX NCBI_TaxID=6741;
RN [1]
RP PROTEIN SEQUENCE.
RC TISSUE=Hepatopancreas;
RX PubMed=2154979; DOI=10.1016/0006-291x(90)91024-m;
RA Klimova O.A., Borukhov S.I., Solovyeva N.I., Balaevskaya T.O.,
RA Strongin A.Y.;
RT "The isolation and properties of collagenolytic proteases from crab
RT hepatopancreas.";
RL Biochem. Biophys. Res. Commun. 166:1411-1420(1990).
CC -!- FUNCTION: This enzyme is a serine protease capable of degrading the
CC native triple helix of collagen.
CC -!- CATALYTIC ACTIVITY:
CC Reaction=Hydrolysis of proteins, with broad specificity for peptide
CC bonds. Native collagen is cleaved about 75% of the length of the
CC molecule from the N-terminus. Low activity on small molecule
CC substrates of both trypsin and chymotrypsin.; EC=3.4.21.32;
CC -!- SIMILARITY: Belongs to the peptidase S1 family. {ECO:0000255|PROSITE-
CC ProRule:PRU00274}.
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DR PIR; D34817; D34817.
DR MEROPS; S01.122; -.
DR GO; GO:0008236; F:serine-type peptidase activity; IEA:UniProtKB-KW.
DR GO; GO:0030574; P:collagen catabolic process; IEA:UniProtKB-KW.
DR GO; GO:0006508; P:proteolysis; IEA:UniProtKB-KW.
PE 1: Evidence at protein level;
KW Collagen degradation; Direct protein sequencing; Hydrolase; Protease;
KW Serine protease.
FT CHAIN 1..>20
FT /note="Collagenolytic protease 36 kDa C"
FT /id="PRO_0000088669"
FT DOMAIN 1..>20
FT /note="Peptidase S1"
FT /evidence="ECO:0000255|PROSITE-ProRule:PRU00274"
FT REGION 1..20
FT /note="Disordered"
FT /evidence="ECO:0000256|SAM:MobiDB-lite"
FT NON_TER 20
SQ SEQUENCE 20 AA; 2129 MW; E9133891C9529B10 CRC64;
IVGGSEATSG QFPYQXSFQD