3L0E
X-ray crystal structure of a Potent Liver X Receptor Modulator
Summary for 3L0E
Entry DOI | 10.2210/pdb3l0e/pdb |
Related | 1P8D 1PQ6 1PQ9 1UPV |
Descriptor | Oxysterols receptor LXR-beta, Nuclear receptor coactivator 2, N-(2-chloro-6-fluorobenzyl)-1-methyl-N-{[3'-(methylsulfonyl)biphenyl-4-yl]methyl}-1H-imidazole-4-sulfonamide, ... (4 entities in total) |
Functional Keywords | hlxr-beta, human liver x receptor-beta, sulfonamide modulator, dna-binding, metal-binding, nucleus, receptor, transcription, transcription regulation, zinc-finger, activator, phosphoprotein |
Biological source | Homo sapiens (human) More |
Cellular location | Nucleus : P55055 Q15596 |
Total number of polymer chains | 2 |
Total formula weight | 30738.47 |
Authors | Gampe Jr., R.T. (deposition date: 2009-12-09, release date: 2010-04-07, Last modification date: 2023-09-06) |
Primary citation | Zuercher, W.J.,Buckholz, R.G.,Campobasso, N.,Collins, J.L.,Galardi, C.M.,Gampe, R.T.,Hyatt, S.M.,Merrihew, S.L.,Moore, J.T.,Oplinger, J.A.,Reid, P.R.,Spearing, P.K.,Stanley, T.B.,Stewart, E.L.,Willson, T.M. Discovery of tertiary sulfonamides as potent liver X receptor antagonists. J.Med.Chem., 53:3412-3416, 2010 Cited by PubMed: 20345102DOI: 10.1021/jm901797p PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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