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Structure paper

TitlePyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis.
Journal, issue, pagesNat. Chem. Biol., Vol. 8, Page 839-847, Year 2012
Publish dateMar 31, 2010 (structure data deposition date)
AuthorsAnastasiou, D. / Yu, Y. / Israelsen, W.J. / Jiang, J.K. / Boxer, M.B. / Hong, B.S. / Tempel, W. / Dimov, S. / Shen, M. / Jha, A. ...Anastasiou, D. / Yu, Y. / Israelsen, W.J. / Jiang, J.K. / Boxer, M.B. / Hong, B.S. / Tempel, W. / Dimov, S. / Shen, M. / Jha, A. / Yang, H. / Mattaini, K.R. / Metallo, C.M. / Fiske, B.P. / Courtney, K.D. / Malstrom, S. / Khan, T.M. / Kung, C. / Skoumbourdis, A.P. / Veith, H. / Southall, N. / Walsh, M.J. / Brimacombe, K.R. / Leister, W. / Lunt, S.Y. / Johnson, Z.R. / Yen, K.E. / Kunii, K. / Davidson, S.M. / Christofk, H.R. / Austin, C.P. / Inglese, J. / Harris, M.H. / Asara, J.M. / Stephanopoulos, G. / Salituro, F.G. / Jin, S. / Dang, L. / Auld, D.S. / Park, H.W. / Cantley, L.C. / Thomas, C.J. / Vander Heiden, M.G.
External linksNat. Chem. Biol. / PubMed:22922757
MethodsX-ray diffraction
Resolution1.95 - 2.1 Å
Structure data

PDB-3me3:
Activator-Bound Structure of Human Pyruvate Kinase M2
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

PDB-3u2z:
Activator-Bound Structure of Human Pyruvate Kinase M2
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-3SZ:
3-{[4-(2,3-dihydro-1,4-benzodioxin-6-ylsulfonyl)-1,4-diazepan-1-yl]sulfonyl}aniline

ChemComp-FBP:
1,6-di-O-phosphono-beta-D-fructofuranose

ChemComp-SO4:
SULFATE ION

ChemComp-UNX:
Unknown entry

ChemComp-HOH:
WATER

ChemComp-07T:
6-(3-aminobenzyl)-4-methyl-2-methylsulfinyl-4,6-dihydro-5H-thieno[2',3':4,5]pyrrolo[2,3-d]pyridazin-5-one

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / activator / Structural Genomics Consortium / SGC / transferase/transferase activator / Structural Genomics / transferase-transferase activator complex

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