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Structure paper

TitleStructures of AMP-activated protein kinase bound to novel pharmacological activators in phosphorylated, non-phosphorylated, and nucleotide-free states.
Journal, issue, pagesJ. Biol. Chem., Vol. 294, Page 953-967, Year 2019
Publish dateJan 26, 2018 (structure data deposition date)
AuthorsYan, Y. / Zhou, X.E. / Novick, S.J. / Shaw, S.J. / Li, Y. / Brunzelle, J.S. / Hitoshi, Y. / Griffin, P.R. / Xu, H.E. / Melcher, K.
External linksJ. Biol. Chem. / PubMed:30478170
MethodsX-ray diffraction
Resolution2.65 - 3.05 Å
Structure data

PDB-6c9f:
AMP-activated protein kinase bound to pharmacological activator R734
Method: X-RAY DIFFRACTION / Resolution: 2.924 Å

PDB-6c9g:
AMP-activated protein kinase bound to pharmacological activator R739
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

PDB-6c9h:
non-phosphorylated AMP-activated protein kinase bound to pharmacological activator R734
Method: X-RAY DIFFRACTION / Resolution: 2.65 Å

PDB-6c9j:
AMP-activated protein kinase bound to pharmacological activator R734
Method: X-RAY DIFFRACTION / Resolution: 3.05 Å

Chemicals

ChemComp-R34:
5-{[6-chloro-5-(1-methyl-1H-indol-5-yl)-1H-benzimidazol-2-yl]oxy}-N-hydroxy-2-methylbenzamide

ChemComp-STU:
STAUROSPORINE / anticancer, antifungal, antibiotic, alkaloid*YM

ChemComp-AMP:
ADENOSINE MONOPHOSPHATE / AMP*YM

ChemComp-R93:
5-{[6-chloro-5-(2'-hydroxy[1,1'-biphenyl]-4-yl)-1H-benzimidazol-2-yl]oxy}-N-hydroxy-2-methylbenzamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / AMPK / activator / crystal / R739 / R734

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