3RVF
FXR with SRC1 and GSK2034
Summary for 3RVF
Entry DOI | 10.2210/pdb3rvf/pdb |
Related | 3RUT 3RUU |
Descriptor | Bile acid receptor, Nuclear receptor coactivator 1, SULFATE ION, ... (5 entities in total) |
Functional Keywords | nuclear receptor, alpha-helical sandwich, transcription factor, rxr, transcription co-factors, bile acid, farnesoid, transcription regulator |
Biological source | Homo sapiens (human) More |
Cellular location | Nucleus . Isoform 1: Nucleus . Isoform 2: Nucleus . Isoform 3: Nucleus . Isoform 4: Nucleus : Q96RI1 Nucleus : Q15788 |
Total number of polymer chains | 2 |
Total formula weight | 30315.49 |
Authors | Williams, S.P.,Madauss, K.P. (deposition date: 2011-05-06, release date: 2011-09-21, Last modification date: 2024-02-28) |
Primary citation | Akwabi-Ameyaw, A.,Caravella, J.A.,Chen, L.,Creech, K.L.,Deaton, D.N.,Madauss, K.P.,Marr, H.B.,Miller, A.B.,Navas, F.,Parks, D.J.,Spearing, P.K.,Todd, D.,Williams, S.P.,Wisely, G.B. Conformationally constrained farnesoid X receptor (FXR) agonists: Alternative replacements of the stilbene. Bioorg.Med.Chem.Lett., 21:6154-6160, 2011 Cited by PubMed Abstract: To further explore the optimum placement of the acid moiety in conformationally constrained analogs of GW 4064 1a, a series of stilbene replacements were prepared. The benzothiophene 1f and the indole 1g display the optimal orientation of the carboxylate for enhanced FXR agonist potency. PubMed: 21890356DOI: 10.1016/j.bmcl.2011.08.034 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.1 Å) |
Structure validation
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