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DCLK1

Nowadays, DCLK1 is a topic that has gained great relevance in both the personal and professional spheres. Since its emergence, DCLK1 has had a significant impact on society, generating debates, reflections and actions that seek to understand and address its implications. Whether locally or globally, DCLK1 has captured the attention of individuals of all ages, contexts and professions, standing out as a central element in contemporary life. This is why it is essential to delve deeper into the analysis of DCLK1, exploring its multiple dimensions and consequences in order to better understand its scope and relevance in today's world.

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DCLK1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDCLK1, CL1, CLICK1, DCAMKL1, DCDC3A, DCLK, doublecortin like kinase 1
External IDsOMIM: 604742; MGI: 1330861; HomoloGene: 130530; GeneCards: DCLK1; OMA:DCLK1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)Chr 13: 35.77 – 36.13 MbChr 3: 55.15 – 55.45 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Doublecortin-like kinase protein 1 (DCLK1)[5][6][7][8] is an enzyme that in humans is encoded by the DCLK1 gene.[5][6][8] Its C-terminal domain in rats is expressed independently from an alternative transcript, cpg16, and can function alone as a serine/threonine protein kinase that is cyclic AMP dependent.[9][10]

DCLK1 expression is a marker for tuft cells, a type of chemosensory cell of the intestinal epithelium.[7][11]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000133083Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027797Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b Omori Y, Suzuki M, Ozaki K, Harada Y, Nakamura Y, Takahashi E, Fujiwara T (Oct 1998). "Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin". J Hum Genet. 43 (3): 169–77. doi:10.1007/s100380050063. PMID 9747029.
  6. ^ a b Sossey-Alaoui K, Srivastava AK (May 1999). "DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX)". Genomics. 56 (1): 121–6. doi:10.1006/geno.1998.5718. PMID 10036192.
  7. ^ a b Ding L, Weygant N, Ding C, Lai Y, Li H (2023). "DCLK1 and tuft cells: Immune-related functions and implications for cancer immunotherapy". Critical Reviews in Oncology and Hematology. 191 104118. doi:10.1016/j.critrevonc.2023.104118. PMID 37660932.
  8. ^ a b "Entrez Gene: DCAMKL1 doublecortin and CaM kinase-like 1". Gene. National Library of Medicine. 7 April 2024. Retrieved 30 May 2024.
  9. ^ Silverman MA, Benard O, Jaaro H, Rattner A, Citri Y, Seger R (1999). "CPG16, a novel protein serine/threonine kinase downstream of cAMP-dependent protein kinase". Journal of Biological Chemistry. 274 (5): 2631–2636. doi:10.1074/jbc.274.5.2631. PMID 9915791.
  10. ^ Lin PT, Gleeson JG, Corbo JC, et al. (2001). "DCAMKL1 encodes a protein kinase with homology to doublecortin that regulates microtubule polymerization". J. Neurosci. 20 (24): 9152–61. doi:10.1523/JNEUROSCI.20-24-09152.2000. PMC 6773030. PMID 11124993.
  11. ^ Gerbe F, Legraverend C, Jay P (2012). "The intestinal epithelium tuft cells: specification and function". Cellular and Molecular Life Sciences. 69 (17): 2907–2917. doi:10.1007/s00018-012-0984-7. PMC 3417095. PMID 22527717.

Further reading

  • Overview of all the structural information available in the PDB for UniProt: O15075 (Serine/threonine-protein kinase DCLK1) at the PDBe-KB.