3TNP
Structure and Allostery of the PKA RIIb Tetrameric Holoenzyme
Summary for 3TNP
Entry DOI | 10.2210/pdb3tnp/pdb |
Related | 3TNQ 3TNR |
Descriptor | cAMP-dependent protein kinase catalytic subunit alpha, cAMP-dependent protein kinase type II-beta regulatory subunit (3 entities in total) |
Functional Keywords | pka riib tetrameric holoenzyme, transferase |
Biological source | Mus musculus (mouse) More |
Cellular location | Cytoplasm: P05132 Cytoplasm (By similarity): P31324 |
Total number of polymer chains | 4 |
Total formula weight | 174022.48 |
Authors | Zhang, P.,Smith-Nguyen, E.V.,Keshwani, M.M.,Deal, M.S.,Kornev, A.P.,Taylor, S.S. (deposition date: 2011-09-01, release date: 2012-02-01, Last modification date: 2024-10-09) |
Primary citation | Zhang, P.,Smith-Nguyen, E.V.,Keshwani, M.M.,Deal, M.S.,Kornev, A.P.,Taylor, S.S. Structure and allostery of the PKA RIIbeta tetrameric holoenzyme Science, 335:712-716, 2012 Cited by PubMed Abstract: In its physiological state, cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA) is a tetramer that contains a regulatory (R) subunit dimer and two catalytic (C) subunits. We describe here the 2.3 angstrom structure of full-length tetrameric RIIβ(2):C(2) holoenzyme. This structure showing a dimer of dimers provides a mechanistic understanding of allosteric activation by cAMP. The heterodimers are anchored together by an interface created by the β4-β5 loop in the RIIβ subunit, which docks onto the carboxyl-terminal tail of the adjacent C subunit, thereby forcing the C subunit into a fully closed conformation in the absence of nucleotide. Diffusion of magnesium adenosine triphosphate (ATP) into these crystals trapped not ATP, but the reaction products, adenosine diphosphate and the phosphorylated RIIβ subunit. This complex has implications for the dissociation-reassociation cycling of PKA. The quaternary structure of the RIIβ tetramer differs appreciably from our model of the RIα tetramer, confirming the small-angle x-ray scattering prediction that the structures of each PKA tetramer are different. PubMed: 22323819DOI: 10.1126/science.1213979 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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