SAMM50
Sorting and assembly machinery component 50 homolog
Also known as: CGI-51, OMP85, SAM50, SAM50_HUMAN, TOB55, TRG-3, YNL026W
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y512
- Gene
- SAMM50
- Ensembl
- ENSG00000100347
- Chromosome
- 22
- Canonical length
- 469 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes a component of the Sorting and Assembly Machinery (SAM) of the mitochondrial outer membrane. The Sam complex functions in the assembly of beta-barrel proteins into the outer mitochondrial membrane.[provided by RefSeq, Jun 2011]
Canonical amino-acid sequenceUniProt
469 residues, UniProt reviewed canonical sequence.
>Q9Y512|SAMM50
1 MGTVHARSLE PLPSSGPDFG GLGEEAEFVE VEPEAKQEIL ENKDVVVQHV HFDGLGRTKD
61 DIIICEIGDV FKAKNLIEVM RKSHEAREKL LRLGIFRQVD VLIDTCQGDD ALPNGLDVTF
121 EVTELRRLTG SYNTMVGNNE GSMVLGLKLP NLLGRAEKVT FQFSYGTKET SYGLSFFKPR
181 PGNFERNFSV NLYKVTGQFP WSSLRETDRG MSAEYSFPIW KTSHTVKWEG VWRELGCLSR
241 TASFAVRKES GHSLKSSLSH AMVIDSRNSS ILPRRGALLK VNQELAGYTG GDVSFIKEDF
301 ELQLNKQLIF DSVFSASFWG GMLVPIGDKP SSIADRFYLG GPTSIRGFSM HSIGPQSEGD
361 YLGGEAYWAG GLHLYTPLPF RPGQGGFGEL FRTHFFLNAG NLCNLNYGEG PKAHIRKLAE
421 CIRWSYGAGI VLRLGNIARL ELNYCVPMGV QTGDRICDGV QFGAGIRFLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SAMM50 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 225 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 225 nTPM
- tongue: 165 nTPM
- parathyroid gland: 108 nTPM
- heart muscle: 63 nTPM
- adrenal gland: 49 nTPM
- duodenum: 48 nTPM
Single-cell type
- parietal cells: 133 nCPM
- esophageal basal cells: 93 nCPM
- oocytes: 88 nCPM
- thymic myoid cells: 82 nCPM
- late primary spermatocytes: 80 nCPM
- erythrocyte progenitors: 77 nCPM
Immune cell
- myeloid DC: 68 nTPM
- MAIT T-cell: 56 nTPM
- memory B-cell: 55 nTPM
- naive B-cell: 51 nTPM
- basophil: 48 nTPM
- eosinophil: 47 nTPM
Brain region
- choroid plexus: 33 nTPM
- pons: 31 nTPM
- cerebellum: 30 nTPM
- medulla oblongata: 30 nTPM
- hypothalamus: 29 nTPM
- midbrain: 28 nTPM
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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.92
- DepMap mean gene effect
- -0.58
- DepMap dependency class
- common
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
- cristae formation
- inner mitochondrial membrane organization
- protein import into mitochondrial matrix
- protein insertion into mitochondrial outer membrane
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Bacterial surface antigen (D15)
- POTRA domain
- Surface antigen D15-like
- Omp85 superfamily domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SAMM50 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 SAMM50 as an antibody target. Whether an autoantibody or antibody against SAMM50 could matter depends on whether native SAMM50 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SAMM50 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SAMM50 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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