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TitleSpecific Clk Inhibitors from a Novel Chemotype for Regulation of Alternative Splicing.
Journal, issue, pagesChem. Biol, Vol. 18, Page 67-, Year 2011
Publish dateAug 31, 2007 (structure data deposition date)
AuthorsFedorov, O. / Huber, K. / Eisenreich, A. / Filippakopoulos, P. / King, O. / Bullock, A.N. / Szklarczyk, D. / Jensen, L.J. / Fabbro, D. / Trappe, J. ...Fedorov, O. / Huber, K. / Eisenreich, A. / Filippakopoulos, P. / King, O. / Bullock, A.N. / Szklarczyk, D. / Jensen, L.J. / Fabbro, D. / Trappe, J. / Rauch, U. / Bracher, F. / Knapp, S.
External linksChem. Biol / PubMed:21276940
MethodsX-ray diffraction
Resolution1.8 - 2.25 Å
Structure data

PDB-2vag:
Crystal structure of di-phosphorylated human CLK1 in complex with a novel substituted indole inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

PDB-2wu6:
Crystal Structure of the Human CLK3 in complex with DKI
Method: X-RAY DIFFRACTION / Resolution: 1.92 Å

PDB-2wu7:
Crystal Structure of the Human CLK3 in complex with V25
Method: X-RAY DIFFRACTION / Resolution: 2.25 Å

Chemicals

ChemComp-V25:
ethyl 3-[(E)-2-amino-1-cyanoethenyl]-6,7-dichloro-1-methyl-1H-indole-2-carboxylate

ChemComp-HOH:
WATER

ChemComp-DKI:
5-AMINO-3-{[4-(AMINOSULFONYL)PHENYL]AMINO}-N-(2,6-DIFLUOROPHENYL)-1H-1,2,4-TRIAZOLE-1-CARBOTHIOAMIDE

ChemComp-SO4:
SULFATE ION

ChemComp-DMS:
DIMETHYL SULFOXIDE / DMSO, precipitant*YM

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-CL:
Unknown entry

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / SERINE/THREONINE-PROTEIN KINASE / TYROSINE-PROTEIN KINASE / NUCLEUS / KINASE / NUCLEOTIDE-BINDING

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