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Structure paper

TitleLuciferin and Derivatives as a Dyrk Selective Scaffold for the Design of Protein Kinase Inhibitors.
Journal, issue, pagesEur. J. Med. Chem., Vol. 94, Page 140-, Year 2015
Publish dateMay 5, 2014 (structure data deposition date)
AuthorsRothweiler, U. / Eriksson, J. / Stensen, W. / Leeson, F. / Engh, R.A. / Svendsen, J.S.
External linksEur. J. Med. Chem. / PubMed:25768698
MethodsX-ray diffraction
Resolution1.851 - 2.1 Å
Structure data

PDB-4d1x:
CDK2 in complex with Luciferin
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

PDB-4d1z:
CDK2 in complex with a Luciferin derivate
Method: X-RAY DIFFRACTION / Resolution: 1.851 Å

Chemicals

ChemComp-ESJ:
(4S)-2-(6-hydroxy-1,3-benzothiazol-2-yl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid

ChemComp-HOH:
WATER

ChemComp-WG8:
(4S)-2-(8-hydroxyquinolin-2-yl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / KINASE / CDK2

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