SGTA
Small glutamine-rich tetratricopeptide repeat-containing protein alpha
Also known as: alphaSGT, hSGT, SGT, SGT1, SGTA_HUMAN, UBP, Vpu
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43765
- Gene
- SGTA
- Ensembl
- ENSG00000104969
- Chromosome
- 19
- Canonical length
- 313 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein which is capable of interacting with the major nonstructural protein of parvovirus H-1 and 70-kDa heat shock cognate protein; however, its function is not known. Since this transcript is expressed ubiquitously in various tissues, this protein may serve a housekeeping function. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
313 residues, UniProt reviewed canonical sequence.
>O43765|SGTA
1 MDNKKRLAYA IIQFLHDQLR HGGLSSDAQE SLEVAIQCLE TAFGVTVEDS DLALPQTLPE
61 IFEAAATGKE MPQDLRSPAR TPPSEEDSAE AERLKTEGNE QMKVENFEAA VHFYGKAIEL
121 NPANAVYFCN RAAAYSKLGN YAGAVQDCER AICIDPAYSK AYGRMGLALS SLNKHVEAVA
181 YYKKALELDP DNETYKSNLK IAELKLREAP SPTGGVGSFD IAGLLNNPGF MSMASNLMNN
241 PQIQQLMSGM ISGGNNPLGT PGTSPSQNDL ASLIQAGQQF AQQMQQQNPE LIEQLRSQIR
301 SRTPSASNDD QQELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SGTA 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 95 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 95 nTPM
- spinal cord: 83 nTPM
- heart muscle: 82 nTPM
- hippocampal formation: 69 nTPM
- liver: 66 nTPM
- cerebral cortex: 66 nTPM
Single-cell type
- syncytiotrophoblasts: 131 nCPM
- esophageal apical cells: 93 nCPM
- early spermatids: 90 nCPM
- late spermatids: 77 nCPM
- migrating cytotrophoblasts: 73 nCPM
- tuft cells: 69 nCPM
Immune cell
- intermediate monocyte: 28 nTPM
- non-classical monocyte: 28 nTPM
- T-reg: 26 nTPM
- myeloid DC: 24 nTPM
- total PBMC: 22 nTPM
- classical monocyte: 22 nTPM
Brain region
- white matter: 69 nTPM
- medulla oblongata: 68 nTPM
- midbrain: 63 nTPM
- spinal cord: 61 nTPM
- cerebral cortex: 61 nTPM
- thalamus: 60 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)
- 0.35
- gnomAD pLI
- 0.95
- gnomAD missense Z
- 1.97
- DepMap mean gene effect
- -0.08
- 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
- ERAD pathway
- negative regulation of ERAD pathway
- negative regulation of ubiquitin-dependent protein catabolic process
- positive regulation of ERAD pathway
- positive regulation of ubiquitin-dependent protein catabolic process
- post-translational protein targeting to endoplasmic reticulum membrane
- tail-anchored membrane protein insertion into ER membrane
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SGTA 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 SGTA as an antibody target. Whether an autoantibody or antibody against SGTA could matter depends on whether native SGTA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SGTA 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 SGTA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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