HIR3P_HIRME
ID HIR3P_HIRME Reviewed; 65 AA.
AC P28508;
DT 01-DEC-1992, integrated into UniProtKB/Swiss-Prot.
DT 01-DEC-1992, sequence version 1.
DT 25-MAY-2022, entry version 99.
DE RecName: Full=Hirudin-3A';
DE AltName: Full=Hirudin IIIA';
OS Hirudo medicinalis (Medicinal leech).
OC Eukaryota; Metazoa; Spiralia; Lophotrochozoa; Annelida; Clitellata;
OC Hirudinea; Hirudinida; Hirudiniformes; Hirudinidae; Hirudo.
OX NCBI_TaxID=6421;
RN [1]
RP PROTEIN SEQUENCE.
RX PubMed=2792365; DOI=10.1016/0014-5793(89)81070-1;
RA Scharf M., Engels J., Tripier D.;
RT "Primary structures of new 'iso-hirudins'.";
RL FEBS Lett. 255:105-110(1989).
CC -!- FUNCTION: Hirudin is a potent thrombin-specific protease inhibitor. It
CC forms a stable non-covalent complex with alpha-thrombin, thereby
CC abolishing its ability to cleave fibrinogen.
CC -!- SUBCELLULAR LOCATION: Secreted.
CC -!- SIMILARITY: Belongs to the protease inhibitor I14 (hirudin) family.
CC {ECO:0000305}.
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DR PIR; S78520; S78520.
DR PDB; 1DWB; X-ray; 3.16 A; I=55-65.
DR PDB; 1DWC; X-ray; 3.00 A; I=55-65.
DR PDB; 1DWD; X-ray; 3.00 A; I=55-65.
DR PDB; 1DWE; X-ray; 3.00 A; I=55-65.
DR PDB; 2CF8; X-ray; 1.30 A; I=56-65.
DR PDB; 2CF9; X-ray; 1.79 A; I=56-65.
DR PDB; 4AYV; X-ray; 2.80 A; D=55-65.
DR PDB; 4AYY; X-ray; 2.60 A; D=55-65.
DR PDB; 4AZ2; X-ray; 2.60 A; D=55-65.
DR PDBsum; 1DWB; -.
DR PDBsum; 1DWC; -.
DR PDBsum; 1DWD; -.
DR PDBsum; 1DWE; -.
DR PDBsum; 2CF8; -.
DR PDBsum; 2CF9; -.
DR PDBsum; 4AYV; -.
DR PDBsum; 4AYY; -.
DR PDBsum; 4AZ2; -.
DR AlphaFoldDB; P28508; -.
DR SMR; P28508; -.
DR Allergome; 9843; Hir me Hirudin.
DR MEROPS; I14.001; -.
DR EvolutionaryTrace; P28508; -.
DR GO; GO:0005576; C:extracellular region; IEA:UniProtKB-SubCell.
DR GO; GO:0004867; F:serine-type endopeptidase inhibitor activity; IEA:UniProtKB-KW.
DR Gene3D; 2.70.10.10; -; 1.
DR InterPro; IPR024793; Hirudin.
DR InterPro; IPR011061; Hirudin/antistatin.
DR InterPro; IPR000429; Prot_inh_hirudin.
DR Pfam; PF00713; Hirudin; 1.
DR PIRSF; PIRSF001640; Hirudin; 1.
DR PRINTS; PR00777; HIRUDIN.
DR SUPFAM; SSF57262; SSF57262; 1.
PE 1: Evidence at protein level;
KW 3D-structure; Direct protein sequencing; Disulfide bond; Glycoprotein;
KW Protease inhibitor; Secreted; Serine protease inhibitor; Sulfation.
FT CHAIN 1..65
FT /note="Hirudin-3A'"
FT /id="PRO_0000195648"
FT REGION 1..3
FT /note="Interaction with thrombin active site"
FT /evidence="ECO:0000250"
FT REGION 32..65
FT /note="Disordered"
FT /evidence="ECO:0000256|SAM:MobiDB-lite"
FT REGION 55..65
FT /note="Interaction with fibrinogen-binding exosite of
FT thrombin"
FT /evidence="ECO:0000250"
FT MOD_RES 63
FT /note="Sulfotyrosine"
FT /evidence="ECO:0000250"
FT CARBOHYD 45
FT /note="O-linked (GalNAc...) threonine"
FT /evidence="ECO:0000250"
FT DISULFID 6..14
FT /evidence="ECO:0000250"
FT DISULFID 16..28
FT /evidence="ECO:0000250"
FT DISULFID 22..39
FT /evidence="ECO:0000250"
FT HELIX 61..63
FT /evidence="ECO:0007829|PDB:4AYY"
SQ SEQUENCE 65 AA; 6973 MW; CA8BE0D72B6449E4 CRC64;
VVYTDCTESG EDLCLCEGSN VCGEGNKCIL GSDGEKNECV TGEGTPKPQS HNDGDFEEIP
EEYLQ