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Structure paper

TitleOrally Active Aminopyridines as Inhibitors of Tetrameric Fructose-1,6-Bisphosphatase.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 3237-, Year 2011
Publish dateJan 14, 2011 (structure data deposition date)
AuthorsHebeisen, P. / Haap, W. / Kuhn, B. / Mohr, P. / Wessel, H.P. / Zutter, U. / Kirchner, S. / Ruf, A. / Benz, J. / Joseph, C. ...Hebeisen, P. / Haap, W. / Kuhn, B. / Mohr, P. / Wessel, H.P. / Zutter, U. / Kirchner, S. / Ruf, A. / Benz, J. / Joseph, C. / Alvarez-Sanchez, R. / Gubler, M. / Schott, B. / Benardeau, A. / Tozzo, E. / Kitas, E.
External linksBioorg. Med. Chem. Lett. / PubMed:21550236
MethodsX-ray diffraction
Resolution2.1 - 2.2 Å
Structure data

PDB-2y5k:
Orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

PDB-2y5l:
orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-YCU:
1-[5-(2-METHOXYETHYL)-4-METHYL-THIOPHEN-2-YL]SULFONYL-3-[4-METHOXY-6-(METHYLCARBAMOYLAMINO)PYRIDIN-2-YL]UREA

ChemComp-HOH:
WATER

ChemComp-RO8:
N-{[(2Z)-5-bromo-1,3-thiazol-2(3H)-ylidene]carbamoyl}-3-chlorobenzenesulfonamide

Source
  • homo sapiens (human)
KeywordsHYDROLASE

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