ULK1
Serine/threonine-protein kinase ULK1
Also known as: ATG1, ATG1A, ULK1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75385
- Gene
- ULK1
- Ensembl
- ENSG00000177169
- Chromosome
- 12
- Canonical length
- 1050 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables identical protein binding activity; protein serine/threonine kinase activity; and small GTPase binding activity. Involved in several processes, including autophagosome assembly; protein phosphorylation; and regulation of autophagy. Located in bounding membrane of organelle; cytosol; and phagophore assembly site membrane. Part of Atg1/ULK1 kinase complex. Is active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1050 residues, UniProt reviewed canonical sequence.
>O75385|ULK1
1 MEPGRGGTET VGKFEFSRKD LIGHGAFAVV FKGRHREKHD LEVAVKCINK KNLAKSQTLL
61 GKEIKILKEL KHENIVALYD FQEMANSVYL VMEYCNGGDL ADYLHAMRTL SEDTIRLFLQ
121 QIAGAMRLLH SKGIIHRDLK PQNILLSNPA GRRANPNSIR VKIADFGFAR YLQSNMMAAT
181 LCGSPMYMAP EVIMSQHYDG KADLWSIGTI VYQCLTGKAP FQASSPQDLR LFYEKNKTLV
241 PTIPRETSAP LRQLLLALLQ RNHKDRMDFD EFFHHPFLDA SPSVRKSPPV PVPSYPSSGS
301 GSSSSSSSTS HLASPPSLGE MQQLQKTLAS PADTAGFLHS SRDSGGSKDS SCDTDDFVMV
361 PAQFPGDLVA EAPSAKPPPD SLMCSGSSLV ASAGLESHGR TPSPSPPCSS SPSPSGRAGP
421 FSSSRCGASV PIPVPTQVQN YQRIERNLQS PTQFQTPRSS AIRRSGSTSP LGFARASPSP
481 PAHAEHGGVL ARKMSLGGGR PYTPSPQVGT IPERPGWSGT PSPQGAEMRG GRSPRPGSSA
541 PEHSPRTSGL GCRLHSAPNL SDLHVVRPKL PKPPTDPLGA VFSPPQASPP QPSHGLQSCR
601 NLRGSPKLPD FLQRNPLPPI LGSPTKAVPS FDFPKTPSSQ NLLALLARQG VVMTPPRNRT
661 LPDLSEVGPF HGQPLGPGLR PGEDPKGPFG RSFSTSRLTD LLLKAAFGTQ APDPGSTESL
721 QEKPMEIAPS AGFGGSLHPG ARAGGTSSPS PVVFTVGSPP SGSTPPQGPR TRMFSAGPTG
781 SASSSARHLV PGPCSEAPAP ELPAPGHGCS FADPITANLE GAVTFEAPDL PEETLMEQEH
841 TEILRGLRFT LLFVQHVLEI AALKGSASEA AGGPEYQLQE SVVADQISLL SREWGFAEQL
901 VLYLKVAELL SSGLQSAIDQ IRAGKLCLSS TVKQVVRRLN ELYKASVVSC QGLSLRLQRF
961 FLDKQRLLDR IHSITAERLI FSHAVQMVQS AALDEMFQHR EGCVPRYHKA LLLLEGLQHM
1021 LSDQADIENV TKCKLCIERR LSALLTGICALocalizationUniProt · AlphaFold · HPA
Whether an antibody against ULK1 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)
- 0.5
- Highest tissue expression
- 77 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 77 nTPM
- basal ganglia: 60 nTPM
- pancreas: 53 nTPM
- pituitary gland: 45 nTPM
- cerebellum: 44 nTPM
- skin: 41 nTPM
Single-cell type
- neutrophils: 208 nCPM
- renal collecting duct intercalated cells: 119 nCPM
- neutrophil progenitors: 94 nCPM
- rod photoreceptor cells: 92 nCPM
- adrenal cortex cells: 92 nCPM
- retinal horizontal cells: 72 nCPM
Immune cell
- neutrophil: 4 nTPM
- plasmacytoid DC: 3.8 nTPM
- eosinophil: 1.4 nTPM
- classical monocyte: 0.9 nTPM
- gdT-cell: 0.4 nTPM
- intermediate monocyte: 0.4 nTPM
Brain region
- basal ganglia: 122 nTPM
- cerebral cortex: 84 nTPM
- hippocampal formation: 77 nTPM
- amygdala: 70 nTPM
- white matter: 51 nTPM
- pons: 49 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)
- 0.29
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.07
- DepMap mean gene effect
- 0.02
- 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
- autophagosome assembly
- autophagy
- axon extension
- cellular response to nutrient levels
- cellular response to stress
- intracellular protein localization
- macroautophagy
- mitophagy
- negative regulation of cell population proliferation
- negative regulation of collateral sprouting
- negative regulation of protein-containing complex assembly
- neuron projection development
- neuron projection regeneration
- peptidyl-serine phosphorylation
- piecemeal microautophagy of the nucleus
- positive regulation of autophagosome assembly
- positive regulation of autophagy
- protein autophosphorylation
- protein phosphorylation
- regulation of autophagy
- regulation of macroautophagy
- regulation of tumor necrosis factor-mediated signaling pathway
- response to starvation
- reticulophagy
- signal transduction
Molecular functions
- ATP binding
- GTPase binding
- identical protein binding
- protein serine kinase activity
- protein serine/threonine kinase activity
- protein-containing complex binding
- small GTPase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein kinase domain
- Serine/threonine-protein kinase, active site
- Protein kinase-like domain superfamily
- Serine/threonine-protein kinase, Ulk1/Ulk2
- Protein kinase, ATP binding site
- Serine/threonine-protein kinase Atg1-like, tMIT domain
- Serine/threonine-protein kinase Atg1-like
- ATG1-like, MIT domain 2
- Protein kinase domain
- Atg1-like, MIT domain 1
- ATG1-like, MIT domain 2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ULK1 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 ULK1 as an antibody target. Whether an autoantibody or antibody against ULK1 could matter depends on whether native ULK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ULK1 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 ULK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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