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FB:nej

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Contents

Species (Taxon ID) Drosophila melanogaster (fruit fly) (taxon:7227)
Gene Name(s) nej ( synonyms: CBP, CBP/Nejire, CBP/p300, CBP_, CG15319, CG15321, CREB binding protein, CREB-binding protein, Cbp, Crbp, Cyclic AMP Response Element Binding protein, Drosophila CREB-binding, Drosophila CREB-binding protein, Nej, Nejire, anon-WO0147981.11, anon-WO03040301.89, cbp, dCBP, dKAT3, dmCBP, l(1)G0112, l(1)G0350, l(1)G0470, lethal (1) G0112, lethal (1) G0350, lethal (1) G0470, nej CBP, p300, p300/CBP, protein )
Protein Name(s) nejire,
External Links
FB FBgn0261617

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0000076

DNA replication checkpoint

FB:FBrf0193226
PMID:17043110[1]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0000123

histone acetyltransferase complex

FB:FBrf0174215

IEA: Inferred from Electronic Annotation

InterPro:IPR014744

C

From FB

GO:0001745

compound eye morphogenesis

FB:FBrf0180303
PMID:15514061[2]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0003713

transcription coactivator activity

FB:FBrf0084865

ISS: Inferred from Sequence or Structural Similarity

F

From FB

GO:0003713

transcription coactivator activity

FB:FBrf0105495

ISS: Inferred from Sequence or Structural Similarity

MGI:MGI:1098280

F

From FB

GO:0003713

transcription coactivator activity

FB:FBrf0125204
PMID:10669739[3]

IGI: Inferred from Genetic Interaction

FB:FBgn0004859

F

From FB

GO:0003713

transcription coactivator activity

FB:FBrf0202091
PMID:17635913[4]

IDA: Inferred from Direct Assay

F

From FB

GO:0003713

transcription coactivator activity

FB:FBrf0202091
PMID:17635913[4]

IGI: Inferred from Genetic Interaction

FB:FBgn0003068

F

From FB

GO:0004402

histone acetyltransferase activity

FB:FBrf0147156
PMID:11997517[5]

IDA: Inferred from Direct Assay

F

From FB

GO:0005515

protein binding

FB:FBrf0145203
PMID:11854460[6]

IPI: Inferred from Physical Interaction

FB:FBgn0002780

F

From FB

GO:0005515

protein binding

FB:FBrf0202091
PMID:17635913[4]

IPI: Inferred from Physical Interaction

FB:FBgn0023076

F

From FB

GO:0005634

nucleus

FB:FBrf0084865

ISS: Inferred from Sequence or Structural Similarity

C

From FB

GO:0005634

nucleus

FB:FBrf0127222
PMID:10774723[7]

IDA: Inferred from Direct Assay

C

From FB

GO:0005634

nucleus

FB:FBrf0145203
PMID:11854460[6]

IDA: Inferred from Direct Assay

C

From FB

GO:0007088

regulation of mitosis

FB:FBrf0160535
PMID:12834870[8]

IGI: Inferred from Genetic Interaction

FB:FBgn0002914

P

From FB

GO:0007088

regulation of mitosis

FB:FBrf0160535
PMID:12834870[8]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0007224

smoothened signaling pathway

FB:FBrf0125204
PMID:10669739[3]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0007224

smoothened signaling pathway

FB:FBrf0135164
PMID:11267889[9]

NAS: Non-traceable Author Statement

P

From FB

GO:0007269

neurotransmitter secretion

FB:FBrf0127222
PMID:10774723[7]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0007416

synapse assembly

FB:FBrf0127222
PMID:10774723[7]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0007464

R3/R4 cell fate commitment

FB:FBrf0180303
PMID:15514061[2]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0008134

transcription factor binding

FB:FBrf0125204
PMID:10669739[3]

IPI: Inferred from Physical Interaction

FB:FBgn0004859

F

From FB

GO:0008140

cAMP response element binding protein binding

FB:FBrf0127222
PMID:10774723[7]

TAS: Traceable Author Statement

F

From FB

GO:0008270

zinc ion binding

FB:FBrf0174215

IEA: Inferred from Electronic Annotation

InterPro:IPR000197
InterPro:IPR000433

F

From FB

GO:0008347

glial cell migration

FB:FBrf0214270
PMID:21213301[10]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0016055

Wnt receptor signaling pathway

FB:FBrf0135164
PMID:11267889[9]

NAS: Non-traceable Author Statement

P

From FB

GO:0022008

neurogenesis

FB:FBrf0214431

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0030097

hemopoiesis

FB:FBrf0167476
PMID:14602069[11]

TAS: Traceable Author Statement

P

From FB

GO:0032922

circadian regulation of gene expression

FB:FBrf0202091
PMID:17635913[4]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0043234

protein complex

FB:FBrf0145203
PMID:11854460[6]

IPI: Inferred from Physical Interaction

FB:FBgn0002780

C

From FB

GO:0043971

histone H3-K18 acetylation

FB:FBrf0208543
PMID:19700617[12]

IDA: Inferred from Direct Assay

P

From FB

GO:0043974

histone H3-K27 acetylation

FB:FBrf0208543
PMID:19700617[12]

IDA: Inferred from Direct Assay

P

From FB

GO:0043982

histone H4-K8 acetylation

FB:FBrf0147156
PMID:11997517[5]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0043983

histone H4-K12 acetylation

FB:FBrf0147156
PMID:11997517[5]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0043993

histone acetyltransferase activity (H3-K18 specific)

FB:FBrf0208543
PMID:19700617[12]

IDA: Inferred from Direct Assay

F

From FB

GO:0044017

histone acetyltransferase activity (H3-K27 specific)

FB:FBrf0208543
PMID:19700617[12]

IDA: Inferred from Direct Assay

F

From FB

GO:0045466

R7 cell differentiation

FB:FBrf0180303
PMID:15514061[2]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0045475

locomotor rhythm

FB:FBrf0202091
PMID:17635913[4]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

FB:FBrf0125204
PMID:10669739[3]

IGI: Inferred from Genetic Interaction

FB:FBgn0004859

P

From FB

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

FB:FBrf0125204
PMID:10669739[3]

IMP: Inferred from Mutant Phenotype

P

From FB

GO:0048749

compound eye development

FB:FBrf0211742
PMID:20065067[13]

IMP: Inferred from Mutant Phenotype

P

From FB


Notes

References

See Help:References for how to manage references in GONUTS.
  1. Smolik S & Jones K (2007) Drosophila dCBP is involved in establishing the DNA replication checkpoint. Mol Cell Biol 27: 135-46 PubMed GONUTS page
  2. 2.0 2.1 2.2 Kumar JP et al. (2004) CREB binding protein functions during successive stages of eye development in Drosophila. Genetics 168: 877-93 PubMed GONUTS page
  3. 3.0 3.1 3.2 3.3 3.4 Chen Y et al. (2000) Cubitus interruptus requires Drosophila CREB-binding protein to activate wingless expression in the Drosophila embryo. Mol Cell Biol 20: 1616-25 PubMed GONUTS page
  4. 4.0 4.1 4.2 4.3 4.4 Hung HC et al. (2007) Circadian transcription depends on limiting amounts of the transcription co-activator nejire/CBP. J Biol Chem 282: 31349-57 PubMed GONUTS page
  5. 5.0 5.1 5.2 Ludlam WH et al. (2002) The acetyltransferase activity of CBP is required for wingless activation and H4 acetylation in Drosophila melanogaster. Mol Cell Biol 22: 3832-41 PubMed GONUTS page
  6. 6.0 6.1 6.2 Bantignies F et al. (2002) The interaction between the coactivator dCBP and Modulo, a chromatin-associated factor, affects segmentation and melanotic tumor formation in Drosophila. Proc Natl Acad Sci U S A 99: 2895-900 PubMed GONUTS page
  7. 7.0 7.1 7.2 7.3 Marek KW et al. (2000) A genetic analysis of synaptic development: pre- and postsynaptic dCBP control transmitter release at the Drosophila NMJ. Neuron 25: 537-47 PubMed GONUTS page
  8. 8.0 8.1 Fung SM et al. (2003) MYB and CBP: physiological relevance of a biochemical interaction. Mech Dev 120: 711-20 PubMed GONUTS page
  9. 9.0 9.1 Fry CJ & Peterson CL (2001) Chromatin remodeling enzymes: who's on first? Curr Biol 11: R185-97 PubMed GONUTS page
  10. Schmidt I et al. (2011) Transcriptional regulation of peripheral glial cell differentiation in the embryonic nervous system of Drosophila. Glia 59: 1264-72 PubMed GONUTS page
  11. Evans CJ et al. (2003) Thicker than blood: conserved mechanisms in Drosophila and vertebrate hematopoiesis. Dev Cell 5: 673-90 PubMed GONUTS page
  12. 12.0 12.1 12.2 12.3 Tie F et al. (2009) CBP-mediated acetylation of histone H3 lysine 27 antagonizes Drosophila Polycomb silencing. Development 136: 3131-41 PubMed GONUTS page
  13. Mallik M & Lakhotia SC (2010) Improved activities of CREB binding protein, heterogeneous nuclear ribonucleoproteins and proteasome following downregulation of noncoding hsromega transcripts help suppress poly(Q) pathogenesis in fly models. Genetics 184: 927-45 PubMed GONUTS page
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