NDUFAB1
Acyl carrier protein, mitochondrial
Also known as: ACP, ACP1, ACPM_HUMAN, FASN2A, SDAP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14561
- Gene
- NDUFAB1
- Ensembl
- ENSG00000004779
- Chromosome
- 16
- Canonical length
- 156 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Enables mitochondrial large ribosomal subunit binding activity. Involved in [2Fe-2S] cluster assembly and protein lipoylation. Located in mitochondrial inner membrane and nucleoplasm. Part of mitochondrial [2Fe-2S] assembly complex and respiratory chain complex I. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
156 residues, UniProt reviewed canonical sequence.
>O14561|NDUFAB1
1 MASRVLSAYV SRLPAAFAPL PRVRMLAVAR PLSTALCSAG TQTRLGTLQP ALVLAQVPGR
61 VTQLCRQYSD MPPLTLEGIQ DRVLYVLKLY DKIDPEKLSV NSHFMKDLGL DSLDQVEIIM
121 AMEDEFGFEI PDIDAEKLMC PQEIVDYIAD KKDVYELocalizationUniProt · AlphaFold · HPA
Whether an antibody against NDUFAB1 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)
- 0.51
- Highest tissue expression
- 613 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 613 nTPM
- skeletal muscle: 412 nTPM
- tongue: 403 nTPM
- liver: 173 nTPM
- kidney: 166 nTPM
- cerebral cortex: 164 nTPM
Single-cell type
- parietal cells: 667 nCPM
- esophageal basal cells: 493 nCPM
- esophageal suprabasal cells: 492 nCPM
- enteric transient amplifying cells: 380 nCPM
- migrating cytotrophoblasts: 371 nCPM
- gastric progenitor cells: 363 nCPM
Immune cell
- plasmacytoid DC: 269 nTPM
- myeloid DC: 240 nTPM
- intermediate monocyte: 223 nTPM
- total PBMC: 205 nTPM
- classical monocyte: 181 nTPM
- T-reg: 178 nTPM
Brain region
- choroid plexus: 91 nTPM
- cerebellum: 85 nTPM
- hypothalamus: 82 nTPM
- cerebral cortex: 82 nTPM
- pons: 79 nTPM
- medulla oblongata: 76 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)
- 0.75
- gnomAD pLI
- 0.53
- gnomAD missense Z
- 0.16
- DepMap mean gene effect
- -0.75
- DepMap dependency class
- common
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
- [2Fe-2S] cluster assembly
- aerobic respiration
- fatty acid biosynthetic process
- iron-sulfur cluster assembly
- mitochondrial electron transport, NADH to ubiquinone
- mitochondrial large ribosomal subunit assembly
- protein lipoylation
- proton motive force-driven mitochondrial ATP synthesis
Molecular functions
- acyl binding
- calcium ion binding
- fatty acid binding
- mitochondrial large ribosomal subunit binding
- structural molecule activity
- acyl carrier activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NDUFAB1 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 NDUFAB1 as an antibody target. Whether an autoantibody or antibody against NDUFAB1 could matter depends on whether native NDUFAB1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NDUFAB1 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 NDUFAB1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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