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2XP9

DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION

Summary for 2XP9
Entry DOI10.2210/pdb2xp9/pdb
Related1F8A 1I6C 1I8G 1I8H 1NMV 1NMW 1PIN 1ZCN 2F21 2XP3 2XP4 2XP5 2XP6 2XP7 2XP8 2XPA 2XPB
DescriptorPEPTIDYL-PROLYL CIS-TRANS ISOMERASE NIMA-INTERACTING 1, DODECAETHYLENE GLYCOL, 4-[BENZYL(CARBOXYMETHYL)CARBAMOYL]-2-PHENYL-1H-IMIDAZOLE-5-CARBOXYLIC ACID, ... (4 entities in total)
Functional Keywordsisomerase, proline directed kinase, cell cycle, oncogenic transformation
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains1
Total formula weight19450.54
Authors
Primary citationPotter, A.,Oldfield, V.,Nunns, C.,Fromont, C.,Ray, S.,Northfield, C.J.,Bryant, C.J.,Scrace, S.F.,Robinson, D.,Matossova, N.,Baker, L.,Dokurno, P.,Surgenor, A.E.,Davis, B.,Richardson, C.M.,Murray, J.B.,Moore, J.D.
Discovery of Cell-Active Phenyl-Imidazole Pin1 Inhibitors by Structure-Guided Fragment Evolution.
Bioorg.Med.Chem.Lett., 20:6483-, 2010
Cited by
PubMed: 20932746
DOI: 10.1016/J.BMCL.2010.09.063
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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