HECW1
E3 ubiquitin-protein ligase HECW1
Also known as: HECW1_HUMAN, KIAA0322, NEDL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q76N89
- Gene
- HECW1
- Ensembl
- ENSG00000002746
- Chromosome
- 7
- Canonical length
- 1606 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoli fibrillar center,Cytosol
OverviewNCBI Gene
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in regulation of dendrite morphogenesis and ubiquitin-dependent protein catabolic process. Predicted to be located in cytosol. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1606 residues, UniProt reviewed canonical sequence.
>Q76N89|HECW1
1 MLLHLCSVKN LYQNRFLGLA AMASPSRNSQ SRRRCKEPLR YSYNPDQFHN MDLRGGPHDG
61 VTIPRSTSDT DLVTSDSRST LMVSSSYYSI GHSQDLVIHW DIKEEVDAGD WIGMYLIDEV
121 LSENFLDYKN RGVNGSHRGQ IIWKIDASSY FVEPETKICF KYYHGVSGAL RATTPSVTVK
181 NSAAPIFKSI GADETVQGQG SRRLISFSLS DFQAMGLKKG MFFNPDPYLK ISIQPGKHSI
241 FPALPHHGQE RRSKIIGNTV NPIWQAEQFS FVSLPTDVLE IEVKDKFAKS RPIIKRFLGK
301 LSMPVQRLLE RHAIGDRVVS YTLGRRLPTD HVSGQLQFRF EITSSIHPDD EEISLSTEPE
361 SAQIQDSPMN NLMESGSGEP RSEAPESSES WKPEQLGEGS VPDGPGNQSI ELSRPAEEAA
421 VITEAGDQGM VSVGPEGAGE LLAQVQKDIQ PAPSAEELAE QLDLGEEASA LLLEDGEAPA
481 STKEEPLEEE ATTQSRAGRE EEEKEQEEEG DVSTLEQGEG RLQLRASVKR KSRPCSLPVS
541 ELETVIASAC GDPETPRTHY IRIHTLLHSM PSAQGGSAAE EEDGAEEEST LKDSSEKDGL
601 SEVDTVAADP SALEEDREEP EGATPGTAHP GHSGGHFPSL ANGAAQDGDT HPSTGSESDS
661 SPRQGGDHSC EGCDASCCSP SCYSSSCYST SCYSSSCYSA SCYSPSCYNG NRFASHTRFS
721 SVDSAKISES TVFSSQDDEE EENSAFESVP DSMQSPELDP ESTNGAGPWQ DELAAPSGHV
781 ERSPEGLESP VAGPSNRREG ECPILHNSQP VSQLPSLRPE HHHYPTIDEP LPPNWEARID
841 SHGRVFYVDH VNRTTTWQRP TAAATPDGMR RSGSIQQMEQ LNRRYQNIQR TIATERSEED
901 SGSQSCEQAP AGGGGGGGSD SEAESSQSSL DLRREGSLSP VNSQKITLLL QSPAVKFITN
961 PEFFTVLHAN YSAYRVFTSS TCLKHMILKV RRDARNFERY QHNRDLVNFI NMFADTRLEL
1021 PRGWEIKTDQ QGKSFFVDHN SRATTFIDPR IPLQNGRLPN HLTHRQHLQR LRSYSAGEAS
1081 EVSRNRGASL LARPGHSLVA AIRSQHQHES LPLAYNDKIV AFLRQPNIFE MLQERQPSLA
1141 RNHTLREKIH YIRTEGNHGL EKLSCDADLV ILLSLFEEEI MSYVPLQAAF HPGYSFSPRC
1201 SPCSSPQNSP GLQRASARAP SPYRRDFEAK LRNFYRKLEA KGFGQGPGKI KLIIRRDHLL
1261 EGTFNQVMAY SRKELQRNKL YVTFVGEEGL DYSGPSREFF FLLSQELFNP YYGLFEYSAN
1321 DTYTVQISPM SAFVENHLEW FRFSGRILGL ALIHQYLLDA FFTRPFYKAL LRLPCDLSDL
1381 EYLDEEFHQS LQWMKDNNIT DILDLTFTVN EEVFGQVTER ELKSGGANTQ VTEKNKKEYI
1441 ERMVKWRVER GVVQQTEALV RGFYEVVDSR LVSVFDAREL ELVIAGTAEI DLNDWRNNTE
1501 YRGGYHDGHL VIRWFWAAVE RFNNEQRLRL LQFVTGTSSV PYEGFAALRG SNGLRRFCIE
1561 KWGKITSLPR AHTCFNRLDL PPYPSYSMLY EKLLTAVEET STFGLELocalizationUniProt · AlphaFold · HPA
Whether an antibody against HECW1 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)
- 0.48
- Highest tissue expression
- 7.6 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 7.6 nTPM
- kidney: 7.3 nTPM
- cerebellum: 3.7 nTPM
- tongue: 2.4 nTPM
- amygdala: 2.1 nTPM
- retina: 2 nTPM
Single-cell type
- retinal horizontal cells: 835 nCPM
- oligodendrocyte progenitor cells: 426 nCPM
- brain excitatory neurons: 340 nCPM
- early spermatids: 288 nCPM
- proximal tubule cells: 279 nCPM
- retinal bipolar cells: 274 nCPM
Immune cell
- basophil: 2.1 nTPM
- neutrophil: 2.1 nTPM
- naive B-cell: 0.8 nTPM
- plasmacytoid DC: 0.7 nTPM
- eosinophil: 0.5 nTPM
- memory B-cell: 0.5 nTPM
Brain region
- cerebral cortex: 83 nTPM
- white matter: 55 nTPM
- basal ganglia: 42 nTPM
- pons: 39 nTPM
- thalamus: 38 nTPM
- cerebellum: 34 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)
- 0.25
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.95
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
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
- negative regulation of canonical Wnt signaling pathway
- protein ubiquitination
- regulation of dendrite morphogenesis
- ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- C2 domain
- HECT domain
- WW domain
- E3 ubiquitin-protein ligase HECW1/2, N-terminal
- C2 domain superfamily
- HECT, E3 ligase catalytic domain
- WW domain superfamily
- E3 ubiquitin-protein ligase HECW, C2 domain
- E3 ubiquitin-protein ligase HECW1, helical box domain
- E3 ubiquitin-protein ligase
- C2 domain
- WW domain
- HECT-domain (ubiquitin-transferase)
- N-terminal domain of E3 ubiquitin-protein ligase HECW1 and 2
- Helical box domain of E3 ubiquitin-protein ligase HECW1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HECW1 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 HECW1 as an antibody target. Whether an autoantibody or antibody against HECW1 could matter depends on whether native HECW1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HECW1 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 HECW1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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