Homo sapiens Protein: BMP1 | |||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-477510.4 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | BMP1 | ||||||||||||||||||||||
Protein Name | bone morphogenetic protein 1 | ||||||||||||||||||||||
Synonyms | OI13; PCOLC; PCP; PCP2; TLD; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000428332 | ||||||||||||||||||||||
InnateDB Gene | IDBG-10398 (BMP1) | ||||||||||||||||||||||
Protein Structure |
![]() |
||||||||||||||||||||||
UniProt Annotation | |||||||||||||||||||||||
Function | Cleaves the C-terminal propeptides of procollagen I, II and III. Induces cartilage and bone formation. May participate in dorsoventral patterning during early development by cleaving chordin (CHRD). Responsible for the proteolytic activation of lysyl oxidase LOX. | ||||||||||||||||||||||
Subcellular Localization | Golgi apparatus, trans-Golgi network {ECO:0000269PubMed:12637569}. Secreted, extracellular space, extracellular matrix {ECO:0000269PubMed:12637569}. Note=Co- localizes with POSTN in the Golgi. {ECO:0000250}. | ||||||||||||||||||||||
Disease Associations | Osteogenesis imperfecta 13 (OI13) [MIM:614856]: An autosomal recessive form of osteogenesis imperfecta, a connective tissue disorder characterized by low bone mass, bone fragility and susceptibility to fractures after minimal trauma. Disease severity ranges from very mild forms without fractures to intrauterine fractures and perinatal lethality. Extraskeletal manifestations, which affect a variable number of patients, are dentinogenesis imperfecta, hearing loss, and blue sclerae. OI13 is characterized by normal teeth, faint blue sclerae, severe growth deficiency, borderline osteoporosis, severe bone deformity, and recurrent fractures affecting both upper and lower limbs. {ECO:0000269PubMed:22052668, ECO:0000269PubMed:22482805}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | Ubiquitous. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
|
||||||||||||||||||||||
Gene Ontology | |||||||||||||||||||||||
Molecular Function |
|
||||||||||||||||||||||
Biological Process |
|
||||||||||||||||||||||
Cellular Component |
|
||||||||||||||||||||||
Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000742
Epidermal growth factor-like domain IPR000859 CUB domain IPR001506 Peptidase M12A, astacin IPR001881 EGF-like calcium-binding domain IPR006026 Peptidase, metallopeptidase IPR015446 Bone morphogenetic protein 1/tolloid-like protein |
||||||||||||||||||||||
PFAM |
PF00008
PF00431 PF01400 PF07645 |
||||||||||||||||||||||
PRINTS |
PR00480
|
||||||||||||||||||||||
PIRSF |
PIRSF001199
|
||||||||||||||||||||||
SMART |
SM00181
SM00042 SM00179 SM00235 |
||||||||||||||||||||||
TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P13497 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P13497 | ||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 649 | ||||||||||||||||||||||
UniGene | Hs.1274 | ||||||||||||||||||||||
RefSeq | |||||||||||||||||||||||
HUGO | HGNC:1067 | ||||||||||||||||||||||
OMIM | 112264 | ||||||||||||||||||||||
CCDS | CCDS34856 | ||||||||||||||||||||||
HPRD | 00209 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AK291620 BC136679 CH471080 L35278 L35279 M22488 U50330 Y08723 Y08724 Y08725 | ||||||||||||||||||||||
GenPept | AAA51833 AAA93462 AAC41703 AAC41710 AAI36680 BAF84309 CAA69973 CAA69974 CAA69975 EAW63698 EAW63703 EAW63704 | ||||||||||||||||||||||