6HKR
Human Cellular Retinoic Acid Binding Protein II (CRABPII) with bound synthetic retinoid DC271.
Summary for 6HKR
| Entry DOI | 10.2210/pdb6hkr/pdb |
| Descriptor | Cellular 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 Keywords | retinoid, fluorescent, dc271, crabpii, signaling protein |
| Biological source | Homo sapiens (Human) |
| Total number of polymer chains | 1 |
| Total formula weight | 16500.93 |
| 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 citation | Tomlinson, 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: 30613343DOI: 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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