ACAD10
Acyl-CoA dehydrogenase family member 10
Also known as: ACD10_HUMAN, MGC5601
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6JQN1
- Gene
- ACAD10
- Ensembl
- ENSG00000111271
- Chromosome
- 12
- Canonical length
- 1059 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes (ACADs), which participate in the beta-oxidation of fatty acids in mitochondria. The encoded enzyme contains a hydrolase domain at the N-terminal portion, a serine/threonine protein kinase catlytic domain in the central region, and a conserved ACAD domain at the C-terminus. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Nov 2008]
Canonical amino-acid sequenceUniProt
1059 residues, UniProt reviewed canonical sequence.
>Q6JQN1|ACAD10
1 MCVRSCFQSP RLQWVWRTAF LKHTQRRHQG SHRWTHLGGS TYRAVIFDMG GVLIPSPGRV
61 AAEWEVQNRI PSGTILKALM EGGENGPWMR FMRAEITAEG FLREFGRLCS EMLKTSVPVD
121 SFFSLLTSER VAKQFPVMTE AITQIRAKGL QTAVLSNNFY LPNQKSFLPL DRKQFDVIVE
181 SCMEGICKPD PRIYKLCLEQ LGLQPSESIF LDDLGTNLKE AARLGIHTIK VNDPETAVKE
241 LEALLGFTLR VGVPNTRPVK KTMEIPKDSL QKYLKDLLGI QTTGPLELLQ FDHGQSNPTY
301 YIRLANRDLV LRKKPPGTLL PSAHAIEREF RIMKALANAG VPVPNVLDLC EDSSVIGTPF
361 YVMEYCPGLI YKDPSLPGLE PSHRRAIYTA MNTVLCKIHS VDLQAVGLED YGKQGDYIPR
421 QVRTWVKQYR ASETSTIPAM ERLIEWLPLH LPRQQRTTVV HGDFRLDNLV FHPEEPEVLA
481 VLDWELSTLG DPLADVAYSC LAHYLPSSFP VLRGINDCDL TQLGIPAAEE YFRMYCLQMG
541 LPPTENWNFY MAFSFFRVAA ILQGVYKRSL TGQASSTYAE QTGKLTEFVS NLAWDFAVKE
601 GFRVFKEMPF TNPLTRSYHT WARPQSQWCP TGSRSYSSVP EASPAHTSRG GLVISPESLS
661 PPVRELYHRL KHFMEQRVYP AEPELQSHQA SAARWSPSPL IEDLKEKAKA EGLWNLFLPL
721 EADPEKKYGA GLTNVEYAHL CELMGTSLYA PEVCNCSAPD TGNMELLVRY GTEAQKARWL
781 IPLLEGKARS CFAMTEPQVA SSDATNIEAS IREEDSFYVI NGHKWWITGI LDPRCQLCVF
841 MGKTDPHAPR HRQQSVLLVP MDTPGIKIIR PLTVYGLEDA PGGHGEVRFE HVRVPKENMV
901 LGPGRGFEIA QGRLGPGRIH HCMRLIGFSE RALALMKARV KSRLAFGKPL VEQGTVLADI
961 AQSRVEIEQA RLLVLRAAHL MDLAGNKAAA LDIAMIKMVA PSMASRVIDR AIQAFGAAGL
1021 SSDYPLAQFF TWARALRFAD GPDEVHRATV AKLELKHRILocalizationUniProt · AlphaFold · HPA
Whether an antibody against ACAD10 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)
- 0.28
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- liver: 21 nTPM
- kidney: 18 nTPM
- parathyroid gland: 18 nTPM
- duodenum: 15 nTPM
- small intestine: 14 nTPM
- heart muscle: 14 nTPM
Single-cell type
- myonuclei: 102 nCPM
- choroid plexus epithelial cells: 82 nCPM
- thyrotrophs: 78 nCPM
- distal convoluted tubule cells: 57 nCPM
- rod photoreceptor cells: 56 nCPM
- adipocytes: 53 nCPM
Immune cell
- non-classical monocyte: 8.7 nTPM
- basophil: 6.9 nTPM
- intermediate monocyte: 6.9 nTPM
- neutrophil: 6.9 nTPM
- classical monocyte: 6.2 nTPM
- myeloid DC: 6.1 nTPM
Brain region
- choroid plexus: 31 nTPM
- white matter: 23 nTPM
- cerebellum: 20 nTPM
- pons: 19 nTPM
- cerebral cortex: 19 nTPM
- basal ganglia: 18 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)
- 1.09
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.37
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Aminoglycoside phosphotransferase
- Acyl-CoA dehydrogenase/oxidase, middle domain
- HAD hydrolase, subfamily IA
- Acyl-CoA dehydrogenase/oxidase, C-terminal
- Acyl-CoA dehydrogenase/oxidase, N-terminal and middle domain superfamily
- Protein kinase-like domain superfamily
- Predicted HAD-superfamily phosphatase, subfamily IA/Epoxide hydrolase, N-terminal
- Acyl-CoA dehydrogenase/oxidase, N-terminal
- Phosphoglycolate phosphatase-like, domain 2
- HAD superfamily
- Acyl-CoA dehydrogenase-like, C-terminal
- HAD-like superfamily
- Acyl-CoA dehydrogenase/oxidase, N-terminal domain superfamily
- Acyl-CoA dehydrogenase family member 10/11, N-terminal
- Acyl-CoA oxidase/dehydrogenase, middle domain superfamily
- Acyl-CoA dehydrogenase, C-terminal domain
- haloacid dehalogenase-like hydrolase
- Phosphotransferase enzyme family
- Acyl-CoA dehydrogenase, middle domain
- Acyl-CoA dehydrogenase, N-terminal domain
- Acyl-CoA dehydrogenase 10-like
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ACAD10 as an antibody target. Whether an autoantibody or antibody against ACAD10 could matter depends on whether native ACAD10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ACAD10 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 ACAD10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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