CREB3
Cyclic AMP-responsive element-binding protein 3
Also known as: CREB3_HUMAN, Luman, LZIP, sLZIP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43889
- Gene
- CREB3
- Ensembl
- ENSG00000107175
- Chromosome
- 9
- Canonical length
- 371 aa
- Protein class
- Predicted membrane proteins, Transcription factors
- Subcellular location
- Vesicles,Plasma membrane,Primary cilium,Primary cilium tip,Primary cilium transition zone,Basal body,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. This protein binds to the cAMP-response element and regulates cell proliferation. The protein interacts with host cell factor C1, which also associates with the herpes simplex virus (HSV) protein VP16 that induces transcription of HSV immediate-early genes. This protein and VP16 both bind to the same site on host cell factor C1. It is thought that the interaction between this protein and host cell factor C1 plays a role in the establishment of latency during HSV infection. This protein also plays a role in leukocyte migration, tumor suppression, and endoplasmic reticulum stress-associated protein degradation. Additional transcript variants have been identified, but their biological validity has not been determined.[provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
371 residues, UniProt reviewed canonical sequence.
>O43889|CREB3
1 MELELDAGDQ DLLAFLLEES GDLGTAPDEA VRAPLDWALP LSEVPSDWEV DDLLCSLLSP
61 PASLNILSSS NPCLVHHDHT YSLPRETVSM DLESESCRKE GTQMTPQHME ELAEQEIARL
121 VLTDEEKSLL EKEGLILPET LPLTKTEEQI LKRVRRKIRN KRSAQESRRK KKVYVGGLES
181 RVLKYTAQNM ELQNKVQLLE EQNLSLLDQL RKLQAMVIEI SNKTSSSSTC ILVLLVSFCL
241 LLVPAMYSSD TRGSLPAEHG VLSRQLRALP SEDPYQLELP ALQSEVPKDS THQWLDGSDC
301 VLQAPGNTSC LLHYMPQAPS AEPPLEWPFP DLFSEPLCRG PILPLQANLT RKGGWLPTGS
361 PSVILQDRYS GLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CREB3 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)
- 0.62
- Highest tissue expression
- 51 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 51 nTPM
- blood vessel: 48 nTPM
- amygdala: 44 nTPM
- cerebral cortex: 43 nTPM
- testis: 43 nTPM
- prostate: 43 nTPM
Single-cell type
- late spermatids: 692 nCPM
- early spermatids: 193 nCPM
- late primary spermatocytes: 103 nCPM
- enterocytes: 82 nCPM
- epididymal principal cells: 79 nCPM
- extravillous trophoblasts: 75 nCPM
Immune cell
- myeloid DC: 38 nTPM
- classical monocyte: 34 nTPM
- intermediate monocyte: 33 nTPM
- plasmacytoid DC: 31 nTPM
- MAIT T-cell: 31 nTPM
- memory CD8 T-cell: 30 nTPM
Brain region
- pons: 36 nTPM
- hypothalamus: 36 nTPM
- midbrain: 36 nTPM
- medulla oblongata: 36 nTPM
- thalamus: 34 nTPM
- basal ganglia: 33 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)
- 1.01
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.04
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chemotaxis
- DNA-templated transcription
- endoplasmic reticulum unfolded protein response
- induction of positive chemotaxis
- integrated stress response signaling
- negative regulation of cell cycle
- negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway
- positive regulation of calcium ion transport
- positive regulation of cell migration
- positive regulation of DNA-templated transcription
- positive regulation of monocyte chemotaxis
- positive regulation of transcription by RNA polymerase II
- regulation of apoptotic process
- regulation of cell growth
- regulation of cell population proliferation
- regulation of transcription by RNA polymerase II
- release from viral latency
- positive regulation of deacetylase activity
Molecular functions
- cAMP response element binding protein binding
- CCR1 chemokine receptor binding
- chromatin binding
- DNA binding
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- identical protein binding
- protein dimerization activity
- protein homodimerization activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- RNA polymerase II transcription regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
- transcription coregulator binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CREB3 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 CREB3 as an antibody target. Whether an autoantibody or antibody against CREB3 could matter depends on whether native CREB3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CREB3 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 CREB3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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