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TargetCyclin-dependent kinase 5
LigandBDBM27344
Substrate/Competitorn/a
Meas. Tech.ChEMBL_653793 (CHEMBL1226915)
IC50 460±n/a nM
Citation Montagnoli, AValsasina, BCroci, VMenichincheri, MRainoldi, SMarchesi, VTibolla, MTenca, PBrotherton, DAlbanese, CPatton, VAlzani, RCiavolella, ASola, FMolinari, AVolpi, DAvanzi, NFiorentini, FCattoni, MHealy, SBallinari, DPesenti, EIsacchi, AMoll, JBensimon, AVanotti, ESantocanale, C A Cdc7 kinase inhibitor restricts initiation of DNA replication and has antitumor activity. Nat Chem Biol4:357-65 (2008) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Cyclin-dependent kinase 5
Name:Cyclin-dependent kinase 5
Synonyms:CDK5 | CDK5_HUMAN | CDKN5 | Cell division protein kinase 5 | Cyclin-dependent kinase 5 (CDK5/ p25) | Cyclin-dependent kinase 5 (CDK5/p35) | Cyclin-dependent-like kinase 5 | Cyclin-dependent-like kinase 5 (CDK5) | PSSALRE | Serine/threonine-protein kinase PSSALRE | Tau protein kinase II catalytic subunit
Type:Enzyme Subunit
Mol. Mass.:33308.61
Organism:Homo sapiens (Human)
Description:n/a
Residue:292
Sequence:
MQKYEKLEKIGEGTYGTVFKAKNRETHEIVALKRVRLDDDDEGVPSSALREICLLKELKH
KNIVRLHDVLHSDKKLTLVFEFCDQDLKKYFDSCNGDLDPEIVKSFLFQLLKGLGFCHSR
NVLHRDLKPQNLLINRNGELKLADFGLARAFGIPVRCYSAEVVTLWYRPPDVLFGAKLYS
TSIDMWSAGCIFAELANAGRPLFPGNDVDDQLKRIFRLLGTPTEEQWPSMTKLPDYKPYP
MYPATTSLVNVVPKLNATGRDLLQNLLKCNPVQRISAEEALQHPYFSDFCPP
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  Blast E-value cutoff:
BDBM27344
n/a
NameBDBM27344
Synonyms:2-(pyridin-4-yl)-1H,4H,5H,6H,7H-pyrrolo[3,2-c]pyridin-4-one | JMC502647 Compound 8 | Pyrrolopyridinone, 1
TypeSmall organic molecule
Emp. Form.C12H11N3O
Mol. Mass.213.2352
SMILESO=C1NCCc2[nH]c(cc12)-c1ccncc1
Structure
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