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6HKR

Human Cellular Retinoic Acid Binding Protein II (CRABPII) with bound synthetic retinoid DC271.

Summary for 6HKR
Entry DOI10.2210/pdb6hkr/pdb
DescriptorCellular retinoic acid-binding protein 2, 1,2-ETHANEDIOL, 4-[2-(4,4-dimethyl-1-propan-2-yl-2,3-dihydroquinolin-6-yl)ethynyl]benzoic acid, ... (6 entities in total)
Functional Keywordsretinoid, fluorescent, dc271, crabpii, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight16500.93
Authors
Tomlinson, C.,Chisholm, D.,Whiting, A.,Pohl, E. (deposition date: 2018-09-07, release date: 2018-11-28, Last modification date: 2024-01-17)
Primary citationTomlinson, C.W.E.,Chisholm, D.R.,Valentine, R.,Whiting, A.,Pohl, E.
Novel Fluorescence Competition Assay for Retinoic Acid Binding Proteins.
ACS Med Chem Lett, 9:1297-1300, 2018
Cited by
PubMed Abstract: Vitamin A derived retinoid compounds have multiple, powerful roles in the cellular growth and development cycle and, as a result, have attracted significant attention from both academic and pharmaceutical research in developing and characterizing synthetic retinoid analogues. Simplifying the hit development workflow for retinoid signaling will improve options available for tackling related pathologies, including tumor growth and neurodegeneration. Here, we present a novel assay that employs an intrinsically fluorescent synthetic retinoid, DC271, which allows direct measurement of the binding of nonlabeled compounds to relevant proteins. The method allows for straightforward initial measurement of binding using existing compound libraries and is followed by calculation of binding constants using a dilution series of plausible hits. The ease of use, high throughput format, and measurement of both qualitative and quantitative binding offer a new direction for retinoid-related pharmacological development.
PubMed: 30613343
DOI: 10.1021/acsmedchemlett.8b00420
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

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