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TitleSynthesis, Biological Evaluation and X-Ray Crystallographic Studies of Imidazo(1,2-A)Pyridine-Based Mycobacterium Tuberculosis Glutamine Synthetase Inhibitors
Journal, issue, pagesMedchemcomm, Vol. 3, Page 620-, Year 2012
Publish dateDec 15, 2011 (structure data deposition date)
AuthorsNordqvist, A. / Nilsson, M.T. / Lagerlund, O. / Muthas, D. / Gising, J. / Yahiaoui, S. / Odell, L.R. / Srinivasa, B.R. / Larhed, M. / Mowbray, S.L. / Karlen, A.
External linksMedchemcomm / Search PubMed
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-4acf:
CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS GLUTAMINE SYNTHETASE IN COMPLEX WITH IMIDAZOPYRIDINE INHIBITOR ((4-(6-BROMO-3-(BUTYLAMINO)IMIDAZO(1,2-A)PYRIDIN-2-YL)PHENOXY) ACETIC ACID) AND L-METHIONINE-S-SULFOXIMINE PHOSPHATE.
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-46B:
{4-[6-BROMO-3-(BUTYLAMINO)IMIDAZO[1,2-A]PYRIDIN-2-YL]PHENOXY}ACETIC ACID

ChemComp-MG:
Unknown entry

ChemComp-P3S:
L-METHIONINE-S-SULFOXIMINE PHOSPHATE

ChemComp-PO4:
PHOSPHATE ION

ChemComp-CL:
Unknown entry

ChemComp-HOH:
WATER

Source
  • mycobacterium tuberculosis (bacteria)
KeywordsLIGASE / NUCLEOTIDE-BINDING / SYNTHETASE / TRI-SUBSTITUTED IMIDAZOLE / TAUT STATE / RV2220 / MT2278 / GLNA1

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