CBR4
3-oxoacyl-[acyl-carrier-protein] reductase
Also known as: CBR4_HUMAN, FLJ14431, SDR45C1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N4T8
- Gene
- CBR4
- Ensembl
- ENSG00000145439
- Chromosome
- 4
- Canonical length
- 237 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homotetramer
OverviewNCBI Gene
Enables several functions, including 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity; NADPH binding activity; and NADPH dehydrogenase (quinone) activity. Involved in fatty acid biosynthetic process; glycoside metabolic process; and protein tetramerization. Located in mitochondrial matrix. Part of oxidoreductase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
237 residues, UniProt reviewed canonical sequence.
>Q8N4T8|CBR4
1 MDKVCAVFGG SRGIGRAVAQ LMARKGYRLA VIARNLEGAK AAAGDLGGDH LAFSCDVAKE
61 HDVQNTFEEL EKHLGRVNFL VNAAGINRDG LLVRTKTEDM VSQLHTNLLG SMLTCKAAMR
121 TMIQQQGGSI VNVGSIVGLK GNSGQSVYSA SKGGLVGFSR ALAKEVARKK IRVNVVAPGF
181 VHTDMTKDLK EEHLKKNIPL GRFGETIEVA HAVVFLLESP YITGHVLVVD GGLQLILLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CBR4 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)
- 0.25
- Highest tissue expression
- 46 nTPM
Expression across tissuesHPA
Tissue
- liver: 46 nTPM
- kidney: 26 nTPM
- epididymis: 19 nTPM
- heart muscle: 17 nTPM
- retina: 16 nTPM
- skeletal muscle: 16 nTPM
Single-cell type
- cardiomyocytes: 5,958 nCPM
- distal convoluted tubule cells: 340 nCPM
- medullary thymic epithelial cells: 326 nCPM
- myonuclei: 304 nCPM
- fibro-adipogenic progenitors: 280 nCPM
- podocytes: 271 nCPM
Immune cell
- basophil: 7.9 nTPM
- naive B-cell: 7.6 nTPM
- gdT-cell: 6.7 nTPM
- eosinophil: 6.4 nTPM
- memory CD8 T-cell: 6.4 nTPM
- naive CD8 T-cell: 6.4 nTPM
Brain region
- white matter: 36 nTPM
- pons: 32 nTPM
- cerebellum: 31 nTPM
- basal ganglia: 31 nTPM
- hypothalamus: 31 nTPM
- thalamus: 31 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)
- 1.7
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.08
- DepMap mean gene effect
- -0.01
- 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
- daunorubicin metabolic process
- doxorubicin metabolic process
- fatty acid biosynthetic process
- fatty-acyl-CoA biosynthetic process
- protein heterotetramerization
- protein homotetramerization
Molecular functions
- 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
- NAD(P)H dehydrogenase (quinone) activity
- NADPH binding
- NADPH dehydrogenase (quinone) activity
- oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
- quinone binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CBR4 as an antibody target. Whether an autoantibody or antibody against CBR4 could matter depends on whether native CBR4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CBR4 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 CBR4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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