Homo sapiens Protein: MSR1 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-8291.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | MSR1 | ||||||||||||||||||||||
Protein Name | macrophage scavenger receptor 1 | ||||||||||||||||||||||
Synonyms | CD204; phSR1; phSR2; SCARA1; SR-A; SRA; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000262101 | ||||||||||||||||||||||
InnateDB Gene | IDBG-8289 (MSR1) | ||||||||||||||||||||||
Protein Structure | |||||||||||||||||||||||
UniProt Annotation | |||||||||||||||||||||||
Function | Membrane glycoproteins implicated in the pathologic deposition of cholesterol in arterial walls during atherogenesis. Two types of receptor subunits exist. These receptors mediate the endocytosis of a diverse group of macromolecules, including modified low density lipoproteins (LDL). Isoform III does not internalize acetylated LDL. | ||||||||||||||||||||||
Subcellular Localization | Membrane; Single-pass type II membrane protein. | ||||||||||||||||||||||
Disease Associations | Prostate cancer (PC) [MIM:176807]: A malignancy originating in tissues of the prostate. Most prostate cancers are adenocarcinomas that develop in the acini of the prostatic ducts. Other rare histopathologic types of prostate cancer that occur in approximately 5% of patients include small cell carcinoma, mucinous carcinoma, prostatic ductal carcinoma, transitional cell carcinoma, squamous cell carcinoma, basal cell carcinoma, adenoid cystic carcinoma (basaloid), signet-ring cell carcinoma and neuroendocrine carcinoma. {ECO:0000269PubMed:12244320}. Note=The disease may be caused by mutations affecting the gene represented in this entry. MSR1 variants may play a role in susceptibility to prostate cancer. MSR1 variants have been found in individuals with prostate cancer and co-segregate with the disease in some families.Barrett esophagus (BE) [MIM:614266]: A condition characterized by a metaplastic change in which normal esophageal squamous epithelium is replaced by a columnar and intestinal-type epithelium. Patients with Barrett esophagus have an increased risk of esophageal adenocarcinoma. The main cause of Barrett esophagus is gastroesophageal reflux. The retrograde movement of acid and bile salts from the stomach into the esophagus causes prolonged injury to the esophageal epithelium and induces chronic esophagitis, which in turn is believed to trigger the pathologic changes. {ECO:0000269PubMed:21791690}. Note=The disease may be caused by mutations affecting the gene represented in this entry. Genetic variants in MSR1 have been found in individuals with Barrett esophagus and are thought to contribute to disease susceptibility. | ||||||||||||||||||||||
Tissue Specificity | Isoform I, isoform II and isoform III are expressed in monocyte-derived macrophages. {ECO:0000269PubMed:9548586}. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR001190
SRCR domain IPR003543 Macrophage scavenger receptor IPR008160 Collagen triple helix repeat IPR015988 STAT transcription factor, coiled coil IPR017448 SRCR-like domain |
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PFAM |
PF00530
PF03523 PF01391 |
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PRINTS |
PR00258
PR01408 |
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PIRSF | |||||||||||||||||||||||
SMART |
SM00202
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P21757 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P21757 | ||||||||||||||||||||||
TrEMBL | E5RFW8 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 4481 | ||||||||||||||||||||||
UniGene | Hs.734231 | ||||||||||||||||||||||
RefSeq | NP_619729 | ||||||||||||||||||||||
HUGO | HGNC:7376 | ||||||||||||||||||||||
OMIM | 153622 | ||||||||||||||||||||||
CCDS | CCDS5995 | ||||||||||||||||||||||
HPRD | 01092 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC010785 AC023396 AC087360 AC091162 AC145059 AF037351 BC063878 CH471080 D13263 D90187 D90188 DQ144993 | ||||||||||||||||||||||
GenPept | AAC09251 AAH63878 AAZ38715 BAA14208 BAA14209 EAW63830 EAW63832 EAW63833 EAW63834 | ||||||||||||||||||||||