ATP6V1D
V-type proton ATPase subunit D
Also known as: ATP6M, VATD, VATD_HUMAN, VMA8
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y5K8
- Gene
- ATP6V1D
- Ensembl
- ENSG00000100554
- Chromosome
- 14
- Canonical length
- 247 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane
OverviewNCBI Gene
This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c"""""""""""""""""""""""""""""""", and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene encodes the V1 domain D subunit protein. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
247 residues, UniProt reviewed canonical sequence.
>Q9Y5K8|ATP6V1D
1 MSGKDRIEIF PSRMAQTIMK ARLKGAQTGR NLLKKKSDAL TLRFRQILKK IIETKMLMGE
61 VMREAAFSLA EAKFTAGDFS TTVIQNVNKA QVKIRAKKDN VAGVTLPVFE HYHEGTDSYE
121 LTGLARGGEQ LAKLKRNYAK AVELLVELAS LQTSFVTLDE AIKITNRRVN AIEHVIIPRI
181 ERTLAYIITE LDEREREEFY RLKKIQEKKK ILKEKSEKDL EQRRAAGEVL EPANLLAEEK
241 DEDLLFELocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATP6V1D 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)
- 0.4
- Highest tissue expression
- 128 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 128 nTPM
- cerebral cortex: 127 nTPM
- kidney: 121 nTPM
- choroid plexus: 121 nTPM
- hypothalamus: 107 nTPM
- tongue: 101 nTPM
Single-cell type
- esophageal apical cells: 1,788 nCPM
- esophageal suprabasal cells: 401 nCPM
- neutrophils: 398 nCPM
- oocytes: 382 nCPM
- syncytiotrophoblasts: 340 nCPM
- parietal cells: 263 nCPM
Immune cell
- basophil: 107 nTPM
- neutrophil: 94 nTPM
- eosinophil: 93 nTPM
- non-classical monocyte: 84 nTPM
- myeloid DC: 84 nTPM
- T-reg: 79 nTPM
Brain region
- pons: 117 nTPM
- cerebral cortex: 114 nTPM
- hypothalamus: 109 nTPM
- basal ganglia: 105 nTPM
- choroid plexus: 105 nTPM
- midbrain: 98 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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.13
- DepMap mean gene effect
- -0.93
- 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
- cilium assembly
- endosomal lumen acidification
- Golgi lumen acidification
- intracellular pH reduction
- lysosomal lumen acidification
- protein localization to cilium
- proton transmembrane transport
- regulation of macroautophagy
- synaptic vesicle lumen acidification
- vacuolar acidification
Molecular functions
- rotational mechanism
- proton-transporting ATPase activity
Cellular components
- centrosome
- cilium
- clathrin-coated vesicle membrane
- cytosol
- endosome membrane
- extracellular exosome
- extrinsic component of synaptic vesicle membrane
- Golgi membrane
- lysosomal membrane
- membrane
- nucleoplasm
- plasma membrane
- proton-transporting V-type ATPase complex
- specific granule membrane
- vacuolar proton-transporting V-type ATPase, V1 domain
Protein domainsUniProt · Pfam · InterPro
- ATPase, V1 complex, subunit D
- ATP synthase subunit D
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ATP6V1D 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 ATP6V1D as an antibody target. Whether an autoantibody or antibody against ATP6V1D could matter depends on whether native ATP6V1D is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATP6V1D 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 ATP6V1D as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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