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Structure paper

TitleAffinity-Based Probes Based on Type II Kinase Inhibitors.
Journal, issue, pagesJ. Am. Chem. Soc., Vol. 134, Page 19017-19025, Year 2012
Publish dateApr 19, 2012 (structure data deposition date)
AuthorsRanjitkar, P. / Perera, B.G. / Swaney, D.L. / Hari, S.B. / Larson, E.T. / Krishnamurty, R. / Merritt, E.A. / Villen, J. / Maly, D.J.
External linksJ. Am. Chem. Soc. / PubMed:23088519
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-4equ:
Human STK-10 (LOK) kinase domain in DFG-out conformation with inhibitor DSA-7
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-G6I:
N-{3-[(3-{4-[(4-methoxyphenyl)amino]-1,3,5-triazin-2-yl}pyridin-2-yl)amino]-4-methylphenyl}-3-(trifluoromethyl)benzamide

ChemComp-CA:
Unknown entry

ChemComp-1PE:
PENTAETHYLENE GLYCOL / precipitant*YM

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / serine/threonine kinase / TRANSFERASE / TRANSFERASE-TRANSFERASE INHIBITOR complex

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