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3U2Z

Activator-Bound Structure of Human Pyruvate Kinase M2

Summary for 3U2Z
Entry DOI10.2210/pdb3u2z/pdb
DescriptorPyruvate kinase isozymes M1/M2, 1,6-di-O-phosphono-beta-D-fructofuranose, UNKNOWN ATOM OR ION, ... (5 entities in total)
Functional Keywordstransferase, structural genomics, structural genomics consortium, sgc, transferase-transferase activator complex, transferase/transferase activator
Biological sourceHomo sapiens (human)
Total number of polymer chains4
Total formula weight234749.33
Authors
Primary citationAnastasiou, 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.
Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis.
Nat.Chem.Biol., 8:839-847, 2012
Cited by
PubMed: 22922757
DOI: 10.1038/nchembio.1060
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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