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Structure paper

TitleStructural basis for exploring the allosteric inhibition of human kidney type glutaminase.
Journal, issue, pagesOncotarget, Vol. 7, Page 57943-57954, Year 2016
Publish dateMay 15, 2016 (structure data deposition date)
AuthorsRamachandran, S. / Pan, C.Q. / Zimmermann, S.C. / Duvall, B. / Tsukamoto, T. / Low, B.C. / Sivaraman, J.
External linksOncotarget / PubMed:27462863
MethodsX-ray diffraction
Resolution2.098 - 2.74 Å
Structure data

PDB-5jyo:
Allosteric inhibition of Kidney Isoform of Glutaminase
Method: X-RAY DIFFRACTION / Resolution: 2.098 Å

PDB-5jyp:
Allosteric inhibition of Kidney Isoform of Glutaminase
Method: X-RAY DIFFRACTION / Resolution: 2.74 Å

Chemicals

ChemComp-63J:
2-(pyridin-2-yl)-N-(5-{4-[6-({[3-(trifluoromethoxy)phenyl]acetyl}amino)pyridazin-3-yl]butyl}-1,3,4-thiadiazol-2-yl)acetamide

ChemComp-HOH:
WATER

ChemComp-ZBS:
2-phenyl-~{N}-[5-[(1~{S},3~{S})-3-[5-(2-phenylethanoylamino)-1,3,4-thiadiazol-2-yl]cyclohexyl]-1,3,4-thiadiazol-2-yl]ethanamide

Source
  • homo sapiens (human)
KeywordsHYDROLASE / KGA / GAC / allosteric inhibition / Warburg effect

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