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7M74

ATP-bound AMP-activated protein kinase

Summary for 7M74
Entry DOI10.2210/pdb7m74/pdb
EMDB information23708
Related PRD IDPRD_900001
Descriptor5'-AMP-activated protein kinase catalytic subunit alpha-1, ADENOSINE-5'-TRIPHOSPHATE, ADENOSINE-5'-DIPHOSPHATE, ... (12 entities in total)
Functional Keywordsampk, activation, atp-binding, signaling protein
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains7
Total formula weight216492.97
Authors
Primary citationYan, Y.,Mukherjee, S.,Harikumar, K.G.,Strutzenberg, T.S.,Zhou, X.E.,Suino-Powell, K.,Xu, T.H.,Sheldon, R.D.,Lamp, J.,Brunzelle, J.S.,Radziwon, K.,Ellis, A.,Novick, S.J.,Vega, I.E.,Jones, R.G.,Miller, L.J.,Xu, H.E.,Griffin, P.R.,Kossiakoff, A.A.,Melcher, K.
Structure of an AMPK complex in an inactive, ATP-bound state.
Science, 373:413-419, 2021
Cited by
PubMed Abstract: Adenosine monophosphate (AMP)-activated protein kinase (AMPK) regulates metabolism in response to the cellular energy states. Under energy stress, AMP stabilizes the active AMPK conformation, in which the kinase activation loop (AL) is protected from protein phosphatases, thus keeping the AL in its active, phosphorylated state. At low AMP:ATP (adenosine triphosphate) ratios, ATP inhibits AMPK by increasing AL dynamics and accessibility. We developed conformation-specific antibodies to trap ATP-bound AMPK in a fully inactive, dynamic state and determined its structure at 3.5-angstrom resolution using cryo-electron microscopy. A 180° rotation and 100-angstrom displacement of the kinase domain fully exposes the AL. On the basis of the structure and supporting biophysical data, we propose a multistep mechanism explaining how adenine nucleotides and pharmacological agonists modulate AMPK activity by altering AL phosphorylation and accessibility.
PubMed: 34437114
DOI: 10.1126/science.abe7565
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.93 Å)
Structure validation

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