NP_001276755.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Related Accession #
Molecular Weight
93,371 Da
NCBI Official Full Name
circadian locomoter output cycles protein kaput isoform 1
NCBI Official Synonym Full Names
circadian locomotor output cycles kaput
NCBI Protein Information
circadian locomoter output cycles protein kaput
UniProt Protein Name
Circadian locomoter output cycles protein kaput
UniProt Synonym Gene Names
UniProt Entry Name
CLOCK_MOUSE
NCBI Summary for CLOCK
The protein encoded by this gene plays a central role in the regulation of circadian rhythms. The protein encodes a transcription factor of the basic helix-loop-helix (bHLH) family and contains DNA binding histone acetyltransferase activity. The encoded protein forms a heterodimer with Arntl (Bmal1) that binds E-box enhancer elements upstream of Period (Per1, Per2, Per3) and Cryptochrome (Cry1, Cry2) genes and activates transcription of these genes. Per and Cry proteins heterodimerize and repress their own transcription by interacting in a feedback loop with Clock/Arntl complexes. Polymorphisms in this gene may be associated with behavioral changes, obesity, and metabolic syndrome. Two transcripts encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2014]
UniProt Comments for CLOCK
CLOCK: ARNTL/2-CLOCK heterodimers activate E-box element (3'- CACGTG-5') transcription of a number of proteins of the circadian clock. Activates transcription of PER1 and PER2. This transcription is inhibited in a feedback loop by PER and CRY proteins. Has intrinsic histone acetyltransferase activity and this enzymatic function contributes to chromatin-remodeling events implicated in circadian control of gene expression. Acetylates primarily histones H3 and H4. Acetylates also a non-histone substrate: ARNTL. Plays a role in DNA damage response (DDR) signaling during the S phase. Component of the circadian clock oscillator which includes the CRY proteins, CLOCK or NPAS2, ARNTL or ARNTL2, CSNK1D and/or CSNK1E, TIMELESS and the PER proteins. Efficient DNA binding requires dimerization with another bHLH protein. Heterodimerization with ARNTL is required for E-box-dependent transactivation, for CLOCK nuclear translocation and degradation, and, for phosphorylation of both CLOCK and ARNTL. Interaction with PER and CRY proteins requires translocation to the nucleus. Interaction of the CLOCK-ARNTL heterodimer with PER or CRY inhibits transcription activation. Binds weakly ARNTL and ARNTL2 to form heterodimers which bind poorly to the E-box motif. Expressed in all tissues examined including spleen, thymus, prostate, testis, ovary, small intestine, colon, leukocytes, heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Highest levels in testis and skeletal muscle. Low levels in thymus, lung and liver. Expressed in all brain regions with highest levels in cerebellum. Highly expressed in the suprachiasmatic nucleus (SCN).
Protein type: Acetyltransferase; DNA-binding; Transcription factor; EC 2.3.1.48
Cellular Component: nucleoplasm; transcription factor complex; intracellular membrane-bound organelle; cytoplasm; chromosome; nucleus
Molecular Function: protein dimerization activity; transferase activity; protein binding; signal transducer activity; histone acetyltransferase activity; DNA binding; chromatin DNA binding; sequence-specific DNA binding; transferase activity, transferring acyl groups; transcription factor activity; transcription factor binding
Biological Process: transcription from RNA polymerase II promoter; circadian rhythm; proteasomal ubiquitin-dependent protein catabolic process; transcription, DNA-dependent; positive regulation of transcription, DNA-dependent; rhythmic process; response to redox state; signal transduction; activation of NF-kappaB transcription factor; regulation of transcription, DNA-dependent; DNA damage checkpoint; positive regulation of transcription from RNA polymerase II promoter; spermatogenesis; circadian regulation of gene expression; histone acetylation; negative regulation of transcription, DNA-dependent; response to DNA damage stimulus; regulation of hair cycle; regulation of insulin secretion; positive regulation of inflammatory response
Research Articles on CLOCK
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Products associated with CLOCK sirna
Pathways associated with CLOCK sirna
Diseases associated with CLOCK sirna
Organs/Tissues associated with CLOCK sirna
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