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4ANM

Complex of CK2 with a CDC7 inhibitor

Summary for 4ANM
Entry DOI10.2210/pdb4anm/pdb
Related1DAW 1DAY 1DS5 1F0Q 1J91 1JAM 1LP4 1LPU 1LR4 1M2P 1M2Q 1M2R 1OM1 1ZOE 1ZOG 1ZOH
DescriptorCASEIN KINASE II SUBUNIT ALPHA, 8-BROMANYL-2-[[(3S)-3-OXIDANYLPYRROLIDIN-1-YL]METHYL]-3H-[1]BENZOFURO[3,2-D]PYRIMIDIN-4-ONE (3 entities in total)
Functional Keywordstransferase
Biological sourceZEA MAYS (MAIZE)
Total number of polymer chains1
Total formula weight39944.58
Authors
Stout, T.J. (deposition date: 2012-03-20, release date: 2012-05-23, Last modification date: 2024-05-01)
Primary citationKoltun, E.S.,Tsuhako, A.L.,Brown, D.S.,Aay, N.,Arcalas, A.,Chan, V.,Du, H.,Engst, S.,Ferguson, K.,Franzini, M.,Galan, A.,Holst, C.R.,Huang, P.,Kane, B.,Kim, M.H.,Li, J.,Markby, D.,Mohan, M.,Noson, K.,Plonowski, A.,Richards, S.J.,Robertson, S.,Shaw, K.,Stott, G.,Stout, T.J.,Young, J.,Yu, P.,Zaharia, C.A.,Zhang, W.,Zhou, P.,Nuss, J.M.,Xu, W.,Kearney, P.C.
Discovery of Xl413, a Potent and Selective Cdc7 Inhibitor.
Bioorg.Med.Chem.Lett., 22:3727-, 2012
Cited by
PubMed: 22560567
DOI: 10.1016/J.BMCL.2012.04.024
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

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