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TitleSynthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a.
Journal, issue, pagesBioorg. Med. Chem., Vol. 16, Page 5452-5464, Year 2008
Publish dateOct 15, 2007 (structure data deposition date)
AuthorsOnda, K. / Suzuki, T. / Shiraki, R. / Yonetoku, Y. / Negoro, K. / Momose, K. / Katayama, N. / Orita, M. / Yamaguchi, T. / Ohta, M. / Tsukamoto, S.
External linksBioorg. Med. Chem. / PubMed:18434170
MethodsX-ray diffraction
Resolution2.45 Å
Structure data

PDB-2zb2:
Human liver glycogen phosphorylase a complexed with glcose and 5-chloro-N-[4-(1,2-dihydroxyethyl)phenyl]-1H-indole-2-carboxamide
Method: X-RAY DIFFRACTION / Resolution: 2.45 Å

Chemicals

ChemComp-GLC:
alpha-D-glucopyranose

ChemComp-MES:
2-(N-MORPHOLINO)-ETHANESULFONIC ACID / pH buffer*YM

ChemComp-PLP:
PYRIDOXAL-5'-PHOSPHATE

ChemComp-A46:
5-chloro-N-{4-[(1R)-1,2-dihydroxyethyl]phenyl}-1H-indole-2-carboxamide

ChemComp-MPD:
(4S)-2-METHYL-2,4-PENTANEDIOL / precipitant*YM

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / ALLOSTERIC SITE / ALLOSTERIC BINDING / Allosteric enzyme / Carbohydrate metabolism / Disease mutation / Glycogen metabolism / Glycogen storage disease / Glycosyltransferase / Nucleotide-binding / Phosphorylation / Pyridoxal phosphate

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