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Ligands
Code Name Style Show Link
FLC Citrate anion
JYI 3-chloro-4-[(E)-2-(5,5-dimethyl-8-phenyl-5,6-dihydronaphthalen-2-yl)ethenyl]benzoic acid
Non-standard Residues
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Glycosylation
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Modification
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Code : 4JYI   PDBj   RCSB PDB   PDBe
Header : Transcription/Agonist
Title : Crystal structure of RARbeta LBD in complex with selective partial agonist BMS641 [3-chloro-4-[(E)-2-(5,5-dimethyl-8-phenyl-5,6-dihydronaphthalen-2-yl)ethenyl]benzoic acid]
Release Data : 2014-03-19
Compound :
mol_id molecule chains synonym
1 Retinoic acid receptor beta A,B RAR-beta, HBV-activated protein, Nuclear receptor subfamily 1 group B member 2, RAR-epsilon
fragment: Ligand binding domain, UNP residues 176-421
mol_id molecule chains synonym
2 Nuclear receptor coactivator 1 F,G SRC-1
ec: 2.3.1.48
fragment: UNP residues 686-698
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:469008)
gene: RARB, HAP, NR1B2
expression_system_strain: BL21 DE3
expression_system_vector_type: PLASMID
expression_system_plasmid: pET15b
mol_id organism_scientific organism_common
2 Homo sapiens  (taxid:9606) Human
synthetic: yes
Authors : Nadendla, E.K., Teyssier, C., Germain, P., Delfosse, V., Bourguet, W.
Keywords : Ligand binding domain, Nuclear hormone receptor, Transcription-Agonist complex
Exp. method : X-RAY DIFFRACTION ( 1.900 Å )
Citation :

An Unexpected Mode Of Binding Defines BMS948 as A Full Retinoic Acid Receptor beta (RAR beta , NR1B2) Selective Agonist.

Nadendla, E.,Teyssier, C.,Delfosse, V.  et al.
(2015)  Plos One  10 : e0123195 - e0123195

PubMed: 25933005
DOI: 10.1371/journal.pone.0123195

Chain : A, B
UniProt : P10826 (RARB_HUMAN)
Reaction : -
Chain : F, G
UniProt : Q15788 (NCOA1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
acetyl-CoA + L-lysyl-[protein] = CoA + H(+) + N(6)-acetyl-L- lysyl-[protein] 2.3.1.48 -
-