ALDH3B2
Aldehyde dehydrogenase family 3 member B2
Also known as: AL3B2_HUMAN, ALDH8
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P48448
- Gene
- ALDH3B2
- Ensembl
- ENSG00000132746
- Chromosome
- 11
- Canonical length
- 385 aa
- Protein class
- Enzymes, FDA approved drug targets, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a member of the aldehyde dehydrogenase family, a group of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The gene of this particular family member is over 10 kb in length. Altered methylation patterns at this locus have been observed in spermatozoa derived from patients exhibiting reduced fecundity. [provided by RefSeq, Aug 2017]
Canonical amino-acid sequenceUniProt
385 residues, UniProt reviewed canonical sequence.
>P48448|ALDH3B2
1 MKDEPRSTNL FMKLDSVFIW KEPFGLVLII APWNYPLNLT LVLLVGALAA GSCVVLKPSE
61 ISQGTEKVLA EVLPQYLDQS CFAVVLGGPQ ETGQLLEHKL DYIFFTGSPR VGKIVMTAAT
121 KHLTPVTLEL GGKNPCYVDD NCDPQTVANR VAWFCYFNAG QTCVAPDYVL CSPEMQERLL
181 PALQSTITRF YGDDPQSSPN LGHIINQKQF QRLRALLGCS RVAIGGQSNE SDRYIAPTVL
241 VDVQETEPVM QEEIFGPILP IVNVQSVDEA IKFINRQEKP LALYAFSNSS QVVNQMLERT
301 SSGSFGGNEG FTYISLLSVP FGGVGHSGMG RYHGKFTFDT FSHHRTCLLA PSGLEKLKEI
361 HYPPYTDWNQ QLLRWGMGSQ SCTLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ALDH3B2 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)
- 0.26
- Highest tissue expression
- 158 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 158 nTPM
- skin: 127 nTPM
- breast: 68 nTPM
- vagina: 43 nTPM
- cervix: 35 nTPM
- tonsil: 20 nTPM
Single-cell type
- esophageal apical cells: 373 nCPM
- esophageal suprabasal cells: 260 nCPM
- esophageal basal cells: 65 nCPM
- suprabasal keratinocytes: 64 nCPM
- endometrial luminal cells: 62 nCPM
- breast hormone-responsive cells: 57 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
- basal ganglia: 0.3 nTPM
- cerebral cortex: 0.2 nTPM
- hypothalamus: 0.2 nTPM
- midbrain: 0.2 nTPM
- medulla oblongata: 0.1 nTPM
- pons: 0.1 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)
- 1.66
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.13
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- alcohol metabolic process
- aldehyde metabolic process
- ethanol catabolic process
- lipid metabolic process
- sphingolipid catabolic process
Molecular functions
- 3-chloroallyl aldehyde dehydrogenase activity
- aldehyde dehydrogenase (NAD+) activity
- aldehyde dehydrogenase [NAD(P)+] activity
- long-chain fatty aldehyde dehydrogenase (NAD+) activity
- medium-chain fatty aldehyde dehydrogenase (NAD+) activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ALDH3B2 as an antibody target. Whether an autoantibody or antibody against ALDH3B2 could matter depends on whether native ALDH3B2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ALDH3B2 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 ALDH3B2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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