EXOC1
Exocyst complex component 1
Also known as: BM-102, EXOC1_HUMAN, FLJ10893, SEC3, SEC3L1, Sec3p
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NV70
- Gene
- EXOC1
- Ensembl
- ENSG00000090989
- Chromosome
- 4
- Canonical length
- 894 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Plasma membrane,Microtubules,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
894 residues, UniProt reviewed canonical sequence.
>Q9NV70|EXOC1
1 MTAIKHALQR DIFTPNDERL LSIVNVCKAG KKKKNCFLCA TVTTERPVQV KVVKVKKSDK
61 GDFYKRQIAW ALRDLAVVDA KDAIKENPEF DLHFEKIYKW VASSTAEKNA FISCIWKLNQ
121 RYLRKKIDFV NVSSQLLEES VPSGENQSVT GGDEEVVDEY QELNAREEQD IEIMMEGCEY
181 AISNAEAFAE KLSRELQVLD GANIQSIMAS EKQVNILMKL LDEALKEVDQ IELKLSSYEE
241 MLQSVKEQMD QISESNHLIH LSNTNNVKLL SEIEFLVNHM DLAKGHIKAL QEGDLASSRG
301 IEACTNAADA LLQCMNVALR PGHDLLLAVK QQQQRFSDLR ELFARRLASH LNNVFVQQGH
361 DQSSTLAQHS VELTLPNHHP FHRDLLRYAK LMEWLKSTDY GKYEGLTKNY MDYLSRLYER
421 EIKDFFEVAK IKMTGTTKES KKFATLPRKE SAVKQETESL HGSSGKLTGS TSSLNKLSVQ
481 SSGNRRSQSS SLLDMGNMSA SDLDVADRTK FDKIFEQVLS ELEPLCLAEQ DFISKFFKLQ
541 QHQSMPGTMA EAEDLDGGTL SRQHNCGTPL PVSSEKDMIR QMMIKIFRCI EPELNNLIAL
601 GDKIDSFNSL YMLVKMSHHV WTAQNVDPAS FLSTTLGNVL VTVKRNFDKC ISNQIRQMEE
661 VKISKKSKVG ILPFVAEFEE FAGLAESIFK NAERRGDLDK AYTKLIRGVF VNVEKVANES
721 QKTPRDVVMM ENFHHIFATL SRLKISCLEA EKKEAKQKYT DHLQSYVIYS LGQPLEKLNH
781 FFEGVEARVA QGIREEEVSY QLAFNKQELR KVIKEYPGKE VKKGLDNLYK KVDKHLCEEE
841 NLLQVVWHSM QDEFIRQYKH FEGLIARCYP GSGVTMEFTI QDILDYCSSI AQSHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EXOC1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 28 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 28 nTPM
- skin: 27 nTPM
- spinal cord: 22 nTPM
- cerebral cortex: 22 nTPM
- spleen: 20 nTPM
- placenta: 20 nTPM
Single-cell type
- esophageal apical cells: 202 nCPM
- adrenal cortex cells: 159 nCPM
- thyrotrophs: 156 nCPM
- oligodendrocytes: 148 nCPM
- lactotrophs: 145 nCPM
- esophageal suprabasal cells: 135 nCPM
Immune cell
- non-classical monocyte: 24 nTPM
- basophil: 21 nTPM
- neutrophil: 20 nTPM
- intermediate monocyte: 19 nTPM
- classical monocyte: 15 nTPM
- myeloid DC: 14 nTPM
Brain region
- white matter: 38 nTPM
- medulla oblongata: 33 nTPM
- thalamus: 31 nTPM
- spinal cord: 30 nTPM
- cerebellum: 30 nTPM
- pons: 30 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)
- 0.48
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.11
- DepMap mean gene effect
- -0.59
- 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
- defense response to virus
- exocytosis
- Golgi to plasma membrane transport
- membrane fission
- mitotic cytokinesis
- protein transport
- regulation of macroautophagy
- vesicle docking involved in exocytosis
- vesicle tethering involved in exocytosis
Molecular functions
- 5-bisphosphate binding
- phosphatidylinositol-4
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Exocyst complex component Sec3, PIP2-binding N-terminal domain
- Exocyst complex component SEC3 N-terminal PIP2 binding PH
- Exocyst complex component Sec3, coiled-coil
- Exocyst complex component Sec3, C-terminal
- Exocyst complex component Sec3, coiled-coil
- Exocyst complex component Sec3, C-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EXOC1 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 EXOC1 as an antibody target. Whether an autoantibody or antibody against EXOC1 could matter depends on whether native EXOC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EXOC1 is annotated at the cell surface, where native EXOC1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label EXOC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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