BNIP3
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3
Also known as: BNIP3_HUMAN, HABON, Nip3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q12983
- Gene
- BNIP3
- Ensembl
- ENSG00000176171
- Chromosome
- 10
- Canonical length
- 194 aa
- Protein class
- Cancer-related genes, Predicted membrane proteins, Transporters
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene is encodes a mitochondrial protein that contains a BH3 domain and acts as a pro-apoptotic factor. The encoded protein interacts with anti-apoptotic proteins, including the E1B 19 kDa protein and Bcl2. This gene is silenced in tumors by DNA methylation. [provided by RefSeq, Dec 2014]
Canonical amino-acid sequenceUniProt
194 residues, UniProt reviewed canonical sequence.
>Q12983|BNIP3
1 MSQNGAPGMQ EESLQGSWVE LHFSNNGNGG SVPASVSIYN GDMEKILLDA QHESGRSSSK
61 SSHCDSPPRS QTPQDTNRAS ETDTHSIGEK NSSQSEEDDI ERRKEVESIL KKNSDWIWDW
121 SSRPENIPPK EFLFKHPKRT ATLSMRNTSV MKKGGIFSAE FLKVFLPSLL LSHLLAIGLG
181 IYIGRRLTTS TSTFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BNIP3 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.6
- Highest tissue expression
- 530 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 530 nTPM
- skeletal muscle: 334 nTPM
- liver: 222 nTPM
- tongue: 163 nTPM
- heart muscle: 145 nTPM
- cerebral cortex: 144 nTPM
Single-cell type
- esophageal apical cells: 1,326 nCPM
- pancreatic acinar cells: 920 nCPM
- extravillous trophoblasts: 673 nCPM
- hepatocytes: 478 nCPM
- migrating cytotrophoblasts: 314 nCPM
- oocytes: 295 nCPM
Immune cell
- naive CD4 T-cell: 48 nTPM
- naive CD8 T-cell: 32 nTPM
- T-reg: 30 nTPM
- memory CD4 T-cell: 29 nTPM
- MAIT T-cell: 22 nTPM
- memory CD8 T-cell: 22 nTPM
Brain region
- hippocampal formation: 170 nTPM
- thalamus: 159 nTPM
- pons: 159 nTPM
- midbrain: 155 nTPM
- cerebellum: 146 nTPM
- medulla oblongata: 139 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)
- 1.46
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.83
- DepMap mean gene effect
- -0.21
- 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
- autophagic cell death
- autophagy of mitochondrion
- brown fat cell differentiation
- cardiac muscle cell apoptotic process
- cellular response to cobalt ion
- cellular response to hydrogen peroxide
- cellular response to hypoxia
- cellular response to mechanical stimulus
- cerebral cortex development
- defense response to virus
- granzyme-mediated programmed cell death signaling pathway
- intrinsic apoptotic signaling pathway in response to hypoxia
- mitochondrial fragmentation involved in apoptotic process
- mitochondrial outer membrane permeabilization
- mitochondrial protein catabolic process
- mitophagy
- negative regulation of apoptotic process
- negative regulation of mitochondrial fusion
- negative regulation of mitochondrial membrane permeability involved in apoptotic process
- negative regulation of mitochondrial membrane potential
- negative regulation of programmed cell death
- neuron apoptotic process
- oligodendrocyte differentiation
- positive regulation of apoptotic process
- positive regulation of autophagy
- positive regulation of autophagy of mitochondrion
- positive regulation of cardiac muscle cell apoptotic process
- positive regulation of macroautophagy
- positive regulation of mitochondrial calcium ion concentration
- positive regulation of mitochondrial fission
- positive regulation of programmed cell death
- positive regulation of protein-containing complex disassembly
- positive regulation of release of cytochrome c from mitochondria
- reactive oxygen species metabolic process
- regulation of mitochondrial membrane permeability
- response to axon injury
- response to bacterium
- response to hyperoxia
- response to hypoxia
- response to oxygen-glucose deprivation
- reticulophagy
- negative regulation of membrane potential
Molecular functions
- endoplasmic reticulum-autophagosome adaptor activity
- GTPase binding
- identical protein binding
- protein homodimerization activity
- mitochondrion autophagosome adaptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BNIP3 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 BNIP3 as an antibody target. Whether an autoantibody or antibody against BNIP3 could matter depends on whether native BNIP3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BNIP3 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 BNIP3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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