NEU4
Sialidase-4
Also known as: NEUR4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WWR8
- Gene
- NEU4
- Ensembl
- ENSG00000204099
- Chromosome
- 2
- Canonical length
- 484 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene belongs to a family of glycohydrolytic enzymes, which remove terminal sialic acid residues from various sialo derivatives, such as glycoproteins, glycolipids, oligosaccharides, and gangliosides. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
484 residues, UniProt reviewed canonical sequence.
>Q8WWR8|NEU4
1 MGVPRTPSRT VLFERERTGL TYRVPSLLPV PPGPTLLAFV EQRLSPDDSH AHRLVLRRGT
61 LAGGSVRWGA LHVLGTAALA EHRSMNPCPV HDAGTGTVFL FFIAVLGHTP EAVQIATGRN
121 AARLCCVASR DAGLSWGSAR DLTEEAIGGA VQDWATFAVG PGHGVQLPSG RLLVPAYTYR
181 VDRRECFGKI CRTSPHSFAF YSDDHGRTWR CGGLVPNLRS GECQLAAVDG GQAGSFLYCN
241 ARSPLGSRVQ ALSTDEGTSF LPAERVASLP ETAWGCQGSI VGFPAPAPNR PRDDSWSVGP
301 GSPLQPPLLG PGVHEPPEEA AVDPRGGQVP GGPFSRLQPR GDGPRQPGPR PGVSGDVGSW
361 TLALPMPFAA PPQSPTWLLY SHPVGRRARL HMGIRLSQSP LDPRSWTEPW VIYEGPSGYS
421 DLASIGPAPE GGLVFACLYE SGARTSYDEI SFCTFSLREV LENVPASPKP PNLGDKPRGC
481 CWPSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NEU4 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
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 79 nTPM
Expression across tissuesHPA
Tissue
- liver: 79 nTPM
- midbrain: 16 nTPM
- colon: 16 nTPM
- hippocampal formation: 15 nTPM
- amygdala: 15 nTPM
- hypothalamus: 14 nTPM
Single-cell type
- oligodendrocyte progenitor cells: 85 nCPM
- oligodendrocytes: 8.7 nCPM
- ependymal cells: 5.9 nCPM
- podocytes: 3.6 nCPM
- proximal tubule cells: 2.5 nCPM
- astrocytes: 1.8 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
- medulla oblongata: 11 nTPM
- white matter: 6.2 nTPM
- midbrain: 5.9 nTPM
- pons: 5.9 nTPM
- thalamus: 5.8 nTPM
- spinal cord: 5.7 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)
- 1.61
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.16
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
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
- ganglioside catabolic process
- glycoprotein catabolic process
- negative regulation of neuron projection development
- oligosaccharide catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NEU4 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 NEU4 as an antibody target. Whether an autoantibody or antibody against NEU4 could matter depends on whether native NEU4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NEU4 is annotated at the cell surface, where native NEU4 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 NEU4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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