MSR1
Macrophage scavenger receptor types I and II
Also known as: CD204, MSRE_HUMAN, SCARA1, SR-A, SR-AI, SR-AII, SR-AIII
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P21757
- Gene
- MSR1
- Ensembl
- ENSG00000038945
- Chromosome
- 8
- Canonical length
- 451 aa
- Protein class
- Cancer-related genes, CD markers, Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
This gene encodes the class A macrophage scavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of this gene. These receptors or isoforms are macrophage-specific trimeric integral membrane glycoproteins and have been implicated in many macrophage-associated physiological and pathological processes including atherosclerosis, Alzheimer's disease, and host defense. The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modified low density lipoproteins (LDLs). The isoform type 3 does not internalize modified LDL (acetyl-LDL) despite having the domain shown to mediate this function in the types 1 and 2 isoforms. It has an altered intracellular processing and is trapped within the endoplasmic reticulum, making it unable to perform endocytosis. The isoform type 3 can inhibit the function of isoforms type 1 and type 2 when co-expressed, indicating a dominant negative effect and suggesting a mechanism for regulation of scavenger receptor activity in macrophages. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
451 residues, UniProt reviewed canonical sequence.
>P21757|MSR1
1 MEQWDHFHNQ QEDTDSCSES VKFDARSMTA LLPPNPKNSP SLQEKLKSFK AALIALYLLV
61 FAVLIPLIGI VAAQLLKWET KNCSVSSTNA NDITQSLTGK GNDSEEEMRF QEVFMEHMSN
121 MEKRIQHILD MEANLMDTEH FQNFSMTTDQ RFNDILLQLS TLFSSVQGHG NAIDEISKSL
181 ISLNTTLLDL QLNIENLNGK IQENTFKQQE EISKLEERVY NVSAEIMAMK EEQVHLEQEI
241 KGEVKVLNNI TNDLRLKDWE HSQTLRNITL IQGPPGPPGE KGDRGPTGES GPRGFPGPIG
301 PPGLKGDRGA IGFPGSRGLP GYAGRPGNSG PKGQKGEKGS GNTLTPFTKV RLVGGSGPHE
361 GRVEILHSGQ WGTICDDRWE VRVGQVVCRS LGYPGVQAVH KAAHFGQGTG PIWLNEVFCF
421 GRESSIEECK IRQWGTRACS HSEDAGVTCT LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MSR1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.51
- Highest tissue expression
- 113 nTPM
Expression across tissuesHPA
Tissue
- lung: 113 nTPM
- gallbladder: 28 nTPM
- placenta: 26 nTPM
- adipose tissue: 24 nTPM
- liver: 23 nTPM
- blood vessel: 19 nTPM
Single-cell type
- kupffer cells: 1,199 nCPM
- cone photoreceptor cells: 706 nCPM
- macrophages: 671 nCPM
- monocytes: 292 nCPM
- renal connecting tubule cells: 285 nCPM
- cdc: 188 nCPM
Immune cell
- intermediate monocyte: 17 nTPM
- non-classical monocyte: 8.7 nTPM
- classical monocyte: 3.3 nTPM
- neutrophil: 3.2 nTPM
- basophil: 1.6 nTPM
- naive B-cell: 1.5 nTPM
Brain region
- white matter: 59 nTPM
- thalamus: 49 nTPM
- medulla oblongata: 43 nTPM
- choroid plexus: 40 nTPM
- pons: 29 nTPM
- spinal cord: 26 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MSR1.
Disease | AllUniProt
Conditions MSR1 is implicated in, by any mechanism.
- Prostate cancer (PC) MIM:176807
- Barrett esophagus (BE) MIM:614266
Disease | GeneticClinVar
8 pathogenic / likely-pathogenic of 138 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Ovarian cancer
- BARRETT ESOPHAGUS/ESOPHAGEAL ADENOCARCINOMA
- Carcinoma of esophagus
Disease | ImmuneIEDB
Conditions an epitope on MSR1 was assayed in.
- rheumatoid arthritis B cell
- osteoarthritis B cell
- Sjogren's syndrome B cell
- systemic lupus erythematosus B cell
- ankylosing spondylitis B cell
- autoimmune disease of musculoskeletal system B cell
- psoriatic arthritis B cell
- gout B cell
- autoimmune vasculitis B cell
- pneumonia B cell
- arthritis B cell
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.7
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.07
- DepMap mean gene effect
- 0.13
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- amyloid-beta clearance
- cholesterol transport
- establishment of localization in cell
- lipoprotein transport
- negative regulation of gene expression
- phagocytosis, engulfment
- plasma lipoprotein particle clearance
- positive regulation of cholesterol storage
- positive regulation of macrophage derived foam cell differentiation
- receptor-mediated endocytosis
Molecular functions
- amyloid-beta binding
- cargo receptor activity
- low-density lipoprotein particle binding
- scavenger receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SRCR domain
- Collagen triple helix repeat
- SRCR-like domain superfamily
- Scavenger receptor cysteine-rich domain
- Collagen triple helix repeat (20 copies)
- Macrophage scavenger receptor, Class A-I/II
- Macrophage scavenger receptor
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MSR1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MSR1 as an antibody target. Whether an autoantibody or antibody against MSR1 could matter depends on whether native MSR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MSR1 is annotated at the cell surface, where native MSR1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label MSR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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