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Structure paper

TitleC-8 Modifications of 3-alkyl-1,8-dibenzylxanthines as inhibitors of human cytosolic phosphoenolpyruvate carboxykinase.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 17, Page 3835-3839, Year 2007
Publish dateApr 7, 2006 (structure data deposition date)
AuthorsPietranico, S.L. / Foley, L.H. / Huby, N. / Yun, W. / Dunten, P. / Vermeulen, J. / Wang, P. / Toth, K. / Ramsey, G. / Gubler, M.L. / Wertheimer, S.J.
External linksBioorg. Med. Chem. Lett. / PubMed:17532214
MethodsX-ray diffraction
Resolution2.3 Å
Structure data

PDB-2gmv:
PEPCK complex with a GTP-competitive inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

Chemicals

ChemComp-MN:
Unknown entry

ChemComp-PEP:
PHOSPHOENOLPYRUVATE

ChemComp-UN8:
N-(4-{[3-BUTYL-1-(2-FLUOROBENZYL)-2,6-DIOXO-2,3,6,7-TETRAHYDRO-1H-PURIN-8-YL]METHYL}PHENYL)-1-METHYL-1H-IMIDAZOLE-4-SULFONAMIDE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsLYASE / GLUCONEOGENESIS / XANTHINE / INHIBITOR

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