CHST4
Carbohydrate sulfotransferase 4
Also known as: CHST4_HUMAN, HEC-GLCNAC-6-ST, LSST
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NCG5
- Gene
- CHST4
- Ensembl
- ENSG00000140835
- Chromosome
- 16
- Canonical length
- 386 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes an N-acetylglucosamine 6-O sulfotransferase. The encoded enzyme transfers sulfate from 3'phosphoadenosine 5'phospho-sulfate to the 6-hydroxyl group of N-acetylglucosamine on glycoproteins. This protein is localized to the Golgi and is involved in the modification of glycan structures on ligands of the lymphocyte homing receptor L-selectin. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]
Canonical amino-acid sequenceUniProt
386 residues, UniProt reviewed canonical sequence.
>Q8NCG5|CHST4
1 MLLPKKMKLL LFLVSQMAIL ALFFHMYSHN ISSLSMKAQP ERMHVLVLSS WRSGSSFVGQ
61 LFGQHPDVFY LMEPAWHVWM TFKQSTAWML HMAVRDLIRA VFLCDMSVFD AYMEPGPRRQ
121 SSLFQWENSR ALCSAPACDI IPQDEIIPRA HCRLLCSQQP FEVVEKACRS YSHVVLKEVR
181 FFNLQSLYPL LKDPSLNLHI VHLVRDPRAV FRSRERTKGD LMIDSRIVMG QHEQKLKKED
241 QPYYVMQVIC QSQLEIYKTI QSLPKALQER YLLVRYEDLA RAPVAQTSRM YEFVGLEFLP
301 HLQTWVHNIT RGKGMGDHAF HTNARDALNV SQAWRWSLPY EKVSRLQKAC GDAMNLLGYR
361 HVRSEQEQRN LLLDLLSTWT VPEQIHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHST4 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)
- 0.26
- Highest tissue expression
- 65 nTPM
Expression across tissuesHPA
Tissue
- gallbladder: 65 nTPM
- pancreas: 12 nTPM
- fallopian tube: 5 nTPM
- liver: 4.1 nTPM
- cervix: 2.3 nTPM
- tonsil: 1.8 nTPM
Single-cell type
- cholangiocytes: 269 nCPM
- pancreatic duct cells: 30 nCPM
- respiratory ciliated cells: 14 nCPM
- fallopian secretory cells: 9.3 nCPM
- epicardial cells: 9.1 nCPM
- parietal cells: 8.8 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 4 nTPM
- midbrain: 1.7 nTPM
- medulla oblongata: 1.2 nTPM
- pons: 1.2 nTPM
- spinal cord: 0.9 nTPM
- hippocampal formation: 0.6 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)
- 1.65
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.26
- DepMap mean gene effect
- -0.06
- 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
- carbohydrate metabolic process
- cell adhesion
- cell-cell signaling
- immune response
- inflammatory response
- N-acetylglucosamine metabolic process
- positive regulation of leukocyte tethering or rolling
- protein O-linked glycosylation via N-acetyl-galactosamine
- protein sulfation
- sulfur compound metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CHST4 as an antibody target. Whether an autoantibody or antibody against CHST4 could matter depends on whether native CHST4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHST4 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 CHST4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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