HS3ST3B1
Heparan sulfate glucosamine 3-O-sulfotransferase 3B1
Also known as: 30ST3B1, 3OST3B1, HS3SB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y662
- Gene
- HS3ST3B1
- Ensembl
- ENSG00000125430
- Chromosome
- 17
- Canonical length
- 390 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
The protein encoded by this gene is a type II integral membrane protein that belongs to the 3-O-sulfotransferases family. These proteins catalyze the addition of sulfate groups at the 3-OH position of glucosamine in heparan sulfate. The substrate specificity of individual members of the family is based on prior modification of the heparan sulfate chain, thus allowing different members of the family to generate binding sites for different proteins on the same heparan sulfate chain. Following treatment with a histone deacetylase inhibitor, expression of this gene is activated in a pancreatic cell line. The increased expression results in promotion of the epithelial-mesenchymal transition. In addition, the modification catalyzed by this protein allows herpes simplex virus membrane fusion and penetration. A very closely related homolog with an almost identical sulfotransferase domain maps less than 1 Mb away. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Canonical amino-acid sequenceUniProt
390 residues, UniProt reviewed canonical sequence.
>Q9Y662|HS3ST3B1
1 MGQRLSGGRS CLDVPGRLLP QPPPPPPPVR RKLALLFAML CVWLYMFLYS CAGSCAAAPG
61 LLLLGSGSRA AHDPPALATA PDGTPPRLPF RAPPATPLAS GKEMAEGAAS PEEQSPEVPD
121 SPSPISSFFS GSGSKQLPQA IIIGVKKGGT RALLEFLRVH PDVRAVGAEP HFFDRSYDKG
181 LAWYRDLMPR TLDGQITMEK TPSYFVTREA PARISAMSKD TKLIVVVRDP VTRAISDYTQ
241 TLSKRPDIPT FESLTFKNRT AGLIDTSWSA IQIGIYAKHL EHWLRHFPIR QMLFVSGERL
301 ISDPAGELGR VQDFLGLKRI ITDKHFYFNK TKGFPCLKKA EGSSRPHCLG KTKGRTHPEI
361 DREVVRRLRE FYRPFNLKFY QMTGHDFGWDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HS3ST3B1 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
- 1
- Mean surface accessibility (rSASA)
- 0.41
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- liver: 27 nTPM
- retina: 11 nTPM
- lymph node: 5.9 nTPM
- salivary gland: 5 nTPM
- tonsil: 4.5 nTPM
- appendix: 4.4 nTPM
Single-cell type
- neutrophils: 331 nCPM
- pdcs: 178 nCPM
- cone photoreceptor cells: 172 nCPM
- neutrophil progenitors: 115 nCPM
- podocytes: 109 nCPM
- lacrimal acinar cells: 106 nCPM
Immune cell
- plasmacytoid DC: 35 nTPM
- T-reg: 26 nTPM
- naive CD4 T-cell: 12 nTPM
- memory CD4 T-cell: 12 nTPM
- naive CD8 T-cell: 12 nTPM
- gdT-cell: 10 nTPM
Brain region
- medulla oblongata: 12 nTPM
- spinal cord: 6.9 nTPM
- midbrain: 5.6 nTPM
- pons: 4.9 nTPM
- choroid plexus: 3.9 nTPM
- thalamus: 3.8 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)
- 0.78
- gnomAD pLI
- 0.29
- gnomAD missense Z
- 0.46
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- branching involved in ureteric bud morphogenesis
- glycosaminoglycan biosynthetic process
- heparan sulfate proteoglycan biosynthetic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HS3ST3B1 as an antibody target. Whether an autoantibody or antibody against HS3ST3B1 could matter depends on whether native HS3ST3B1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HS3ST3B1 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 HS3ST3B1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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