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Structure paper

TitleStructural Analysis of the Binding of Type I, I1/2, and II Inhibitors to Eph Tyrosine Kinases.
Journal, issue, pagesAcs Med. Chem. Lett., Vol. 6, Page 79-83, Year 2015
Publish dateJul 1, 2014 (structure data deposition date)
AuthorsDong, J. / Zhao, H. / Zhou, T. / Spiliotopoulos, D. / Rajendran, C. / Li, X.D. / Huang, D. / Caflisch, A.
External linksAcs Med. Chem. Lett. / PubMed:25589935
MethodsX-ray diffraction
Resolution1.706 - 2.047 Å
Structure data

PDB-4twn:
Human EphA3 Kinase domain in complex with Birb796
Method: X-RAY DIFFRACTION / Resolution: 1.706 Å

PDB-4two:
Human EphA3 Kinase domain in complex with compound 164
Method: X-RAY DIFFRACTION / Resolution: 2.047 Å

Chemicals

ChemComp-B96:
1-(5-TERT-BUTYL-2-P-TOLYL-2H-PYRAZOL-3-YL)-3-[4-(2-MORPHOLIN-4-YL-ETHOXY)-NAPHTHALEN-1-YL]-UREA

ChemComp-HOH:
WATER

ChemComp-37W:
5-{[3-carbamoyl-4-(3,4-dimethylphenyl)-5-methylthiophen-2-yl]amino}-5-oxopentanoic acid

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / TRANSFERASE/TRANSFERASE INHIBITOR

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