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4JV4

Crystal Structure of RIalpha(91-379) bound to HE33, a N6 di-propyl substituted cAMP analog

Summary for 4JV4
Entry DOI10.2210/pdb4jv4/pdb
Related1NE4 1NE6 1RGS
DescriptorcAMP-dependent protein kinase type I-alpha regulatory subunit, (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 (2 entities in total)
Functional Keywordscamp-dependent protein kinase, cyclic nucleotide analogs, isoform selectivity, fluorescence anisotropy, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceBos taurus (bovine,cow,domestic cattle,domestic cow)
Cellular locationCell membrane (By similarity): P00514
Total number of polymer chains1
Total formula weight33320.58
Authors
Brown, S.H.J.,Cheng, C.Y.,Saldanha, A.S.,Wu, J.,Cottam, H.,Sankaran, B.,Taylor, S.S. (deposition date: 2013-03-25, release date: 2013-09-18, Last modification date: 2023-09-20)
Primary citationBrown, S.H.,Cheng, C.Y.,Saldanha, S.A.,Wu, J.,Cottam, H.B.,Sankaran, B.,Taylor, S.S.
Implementing Fluorescence Anisotropy Screening and Crystallographic Analysis to Define PKA Isoform-Selective Activation by cAMP Analogs.
Acs Chem.Biol., 8:2164-2172, 2013
Cited by
PubMed: 23978166
DOI: 10.1021/cb400247t
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.952 Å)
Structure validation

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