In this article, the topic of CDKL2 will be addressed from different perspectives and discussions. CDKL2 is a topic that has sparked interest and debate in various areas, generating great expectations among experts and the general public. In the following lines, the implications, repercussions and possible solutions related to CDKL2 will be explored, in order to offer a comprehensive and enlightening vision on this topic. Furthermore, different opinions and approaches will be taken into account to enrich the analysis and provide a multidimensional view of CDKL2.
Cyclin-dependent kinase-like 2 is an enzyme that in humans is encoded by the CDKL2gene.[5][6]
This gene product is a member of a large family of CDC2-related serine/threonine protein kinases. It accumulates primarily in the cytoplasm, with lower levels in the nucleus.[6]
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Taglienti CA, Wysk M, Davis RJ (Feb 1997). "Molecular cloning of the epidermal growth factor-stimulated protein kinase p56 KKIAMRE". Oncogene. 13 (12): 2563–74. PMID9000130.
Overview of all the structural information available in the PDB for UniProt: Q92772 (Cyclin-dependent kinase-like 2) at the PDBe-KB.
Further reading
Marracci GH, Marquardt WE, Strehlow A, et al. (2006). "Lipoic acid downmodulates CD4 from human T lymphocytes by dissociation of p56(Lck)". Biochem. Biophys. Res. Commun. 344 (3): 963–971. doi:10.1016/j.bbrc.2006.03.172. PMID16631599.
Sarkar SN, Peters KL, Elco CP, et al. (2004). "Novel roles of TLR3 tyrosine phosphorylation and PI3 kinase in double-stranded RNA signaling". Nat. Struct. Mol. Biol. 11 (11): 1060–1067. doi:10.1038/nsmb847. PMID15502848. S2CID6869429.