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Structure paper

TitleImplementing Fluorescence Anisotropy Screening and Crystallographic Analysis to Define PKA Isoform-Selective Activation by cAMP Analogs.
Journal, issue, pagesAcs Chem. Biol., Vol. 8, Page 2164-2172, Year 2013
Publish dateMar 25, 2013 (structure data deposition date)
AuthorsBrown, S.H. / Cheng, C.Y. / Saldanha, S.A. / Wu, J. / Cottam, H.B. / Sankaran, B. / Taylor, S.S.
External linksAcs Chem. Biol. / PubMed:23978166
MethodsX-ray diffraction
Resolution2.5 - 2.952 Å
Structure data

PDB-4jv4:
Crystal Structure of RIalpha(91-379) bound to HE33, a N6 di-propyl substituted cAMP analog
Method: X-RAY DIFFRACTION / Resolution: 2.952 Å

PDB-4jva:
Crystal Structure of RIIbeta(108-402) bound to HE33, a N6 di-propyl substituted cAMP analog
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

Chemicals

ChemComp-1OR:
(2R,4aR,6R,7R,7aS)-6-[6-(dipropylamino)-9H-purin-9-yl]tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol 2-oxide

ChemComp-HOH:
WATER

Source
  • bos taurus (domestic cattle)
  • rattus norvegicus (Norway rat)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / cAMP-dependent protein kinase / cyclic nucleotide analogs / isoform selectivity / fluorescence anisotropy / TRANSFERASE-TRANSFERASE INHIBITOR complex

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