Bone Morphogenetic Protein 1
Bone Morphogenetic Protein 1 | ||
---|---|---|
according to 3EDG | ||
Properties of human protein | ||
Mass / length primary structure | 866 amino acids | |
Cofactor | Zn 2+ , Ca 2+ | |
Isoforms | 7th | |
Identifier | ||
Gene name | BMP1 | |
External IDs | ||
Enzyme classification | ||
EC, category | 3.4.24.19 , metalloprotease | |
MEROPS | M12.005 | |
Response type | Cleavage of peptide bonds | |
Substrate | Ala - + - Asp / Arg - + - Asp in Procollagen-I / II / III and Pro-ApoA1 | |
Products | Collagen-I / II / III, ApoA1 | |
Occurrence | ||
Parent taxon | multicellular animals | |
Orthologue | ||
human | House mouse | |
Entrez | 649 | 12153 |
Ensemble | ENSG00000168487 | ENSMUSG00000022098 |
UniProt | P13497 | P98063 |
Refseq (mRNA) | NM_001199 | NM_009755 |
Refseq (protein) | NP_001190 | NP_033885 |
Gene locus | Chr 8: 22.16 - 22.21 Mb | Chr 14: 70.47 - 70.52 Mb |
PubMed search | 649 |
12153
|
Bone morphogenetic protein 1 (BMP1) is a protein whose homologues can be detected in all multicellular animals . In humans, BMP1 has on the one hand the function of a growth factor that can trigger the differentiation of mesenchymal cells into osteoblasts , on the other hand BMP1 has enzymatic activity: as a peptidase , it cleaves the precursors of collagens I, II and III as well as apolipoprotein A1 . It is therefore important for cartilage formation and reverse cholesterol transport . BMP1 is the only bone morphogenetic protein that does not belong to the TGF-beta superfamily ( transforming growth factor ) of cytokines . BMP1 belongs to the metalloproteases .
BMP1 inhibitors have shown the potential to be used in scar creams in cell and animal studies .
Individual evidence
- ↑ Homologues at OMA
- ↑ UniProt P13497
- ↑ H. Ibelgaufts / COPE: BMP
- ↑ Chau P, Fielding PE, Fielding CJ: Bone morphogenetic protein-1 (BMP-1) cleaves human proapolipoprotein A1 and regulates its activation for lipid binding . In: Biochemistry . 46, No. 28, July 2007, pp. 8445-50. doi : 10.1021 / bi700028u . PMID 17580958 .
- ^ Bailey S, Fish PV, Billotte S, et al. : Succinyl hydroxamates as potent and selective non-peptidic inhibitors of procollagen C-proteinase: design, synthesis, and evaluation as topically applied, dermal anti-scarring agents . In: Bioorg. Med. Chem. Lett. . 18, No. 24, December 2008, pp. 6562-7. doi : 10.1016 / j.bmcl.2008.10.036 . PMID 18945617 .
- ↑ Reid RR, Mogford JE, R Butt, Degiorgio-Miller A, Mustoe TA: Inhibition of procollagen C-proteinase Reduce scar hypertrophy in a rabbit model of cutaneous scarring . In: Wound Repair Regen . 14, No. 2, 2006, pp. 138-41. doi : 10.1111 / j.1743-6109.2006.00103.x . PMID 16630102 .
- ↑ Zhang Y, Ge G, Greenspan DS: Inhibition of bone morphogenetic protein 1 by native and altered forms of alpha2-macroglobulin . In: J. Biol. Chem. . 281, No. 51, December 2006, pp. 39096-104. doi : 10.1074 / jbc.M601362200 . PMID 17071617 .
Web links
- D'Eustachio / Jassal / reactome: Conversion of pro-apoA-I to apoA-I