NUBP2
Cytosolic Fe-S cluster assembly factor NUBP2
Also known as: CFD1, CIAO6, NUBP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y5Y2
- Gene
- NUBP2
- Ensembl
- ENSG00000095906
- Chromosome
- 16
- Canonical length
- 271 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes an adenosine triphosphate (ATP) and metal-binding protein that is required for the assembly of cyotosolic iron-sulfur proteins. The encoded protein functions in a heterotetramer with nucleotide-binding protein 1 (NUBP1). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2013]
Canonical amino-acid sequenceUniProt
271 residues, UniProt reviewed canonical sequence.
>Q9Y5Y2|NUBP2
1 MEAAAEPGNL AGVRHIILVL SGKGGVGKST ISTELALALR HAGKKVGILD VDLCGPSIPR
61 MLGAQGRAVH QCDRGWAPVF LDREQSISLM SVGFLLEKPD EAVVWRGPKK NALIKQFVSD
121 VAWGELDYLV VDTPPGTSDE HMATIEALRP YQPLGALVVT TPQAVSVGDV RRELTFCRKT
181 GLRVMGIVEN MSGFTCPHCT ECTSVFSRGG GEELAQLAGV PFLGSVPLDP ALMRTLEEGH
241 DFIQEFPGSP AFAALTSIAQ KILDATPACL PLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NUBP2 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
- 57 nTPM
Expression across tissuesHPA
Tissue
- liver: 57 nTPM
- pancreas: 37 nTPM
- adrenal gland: 37 nTPM
- choroid plexus: 35 nTPM
- esophagus: 33 nTPM
- kidney: 33 nTPM
Single-cell type
- late spermatids: 169 nCPM
- esophageal basal cells: 129 nCPM
- cytotrophoblasts: 121 nCPM
- migrating cytotrophoblasts: 107 nCPM
- esophageal suprabasal cells: 96 nCPM
- extravillous trophoblasts: 95 nCPM
Immune cell
- plasmacytoid DC: 88 nTPM
- T-reg: 84 nTPM
- basophil: 72 nTPM
- total PBMC: 68 nTPM
- gdT-cell: 65 nTPM
- myeloid DC: 62 nTPM
Brain region
- choroid plexus: 35 nTPM
- medulla oblongata: 24 nTPM
- white matter: 20 nTPM
- basal ganglia: 20 nTPM
- cerebellum: 20 nTPM
- cerebral cortex: 20 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)
- 1.2
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.07
- DepMap mean gene effect
- -0.62
- 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
Molecular functions
- 4 iron, 4 sulfur cluster binding
- ATP binding
- ATP-dependent FeS chaperone activity
- iron-sulfur cluster binding
- metal ion binding
- nucleotide binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Iron-sulfur cluster carrier protein-like, conserved site
- Mrp/NBP35 ATP-binding protein
- P-loop containing nucleoside triphosphate hydrolase
- Flagellum site-determining protein YlxH/ Fe-S cluster assembling factor NBP35
- NUBPL iron-transfer P-loop NTPase
- Cytosolic Fe-S cluster assembly factor NUBP2/Cfd1, eukaryotes
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NUBP2 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 NUBP2 as an antibody target. Whether an autoantibody or antibody against NUBP2 could matter depends on whether native NUBP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NUBP2 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 NUBP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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