3FEP
Crystal structure of the R132K:R111L:L121E:R59W-CRABPII mutant complexed with a synthetic ligand (merocyanin) at 2.60 angstrom resolution.
3FEP の概要
| エントリーDOI | 10.2210/pdb3fep/pdb |
| 関連するPDBエントリー | 2fr3 2fs6 2g7b 3f8a 3FEK 3FEL 3FEN |
| 分子名称 | Cellular retinoic acid-binding protein 2, (2E,4E,6E)-3-methyl-6-(1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene)hexa-2,4-dienal, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, ... (4 entities in total) |
| 機能のキーワード | merocyanin, crabpii, retinoic acid, retinoid, psb, protonated schiff base, fluorescence, crabp, nucleus, retinol-binding, transport, vitamin a, transport protein |
| 由来する生物種 | Homo sapiens (Human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 16017.33 |
| 構造登録者 | |
| 主引用文献 | Yapici, I.,Lee, K.S.,Berbasova, T.,Nosrati, M.,Jia, X.,Vasileiou, C.,Wang, W.,Santos, E.M.,Geiger, J.H.,Borhan, B. "Turn-on" protein fluorescence: in situ formation of cyanine dyes. J.Am.Chem.Soc., 137:1073-1080, 2015 Cited by PubMed Abstract: Protein reengineering of cellular retinoic acid binding protein II (CRABPII) has yielded a genetically addressable system, capable of binding a profluorophoric chromophore that results in fluorescent protein/chromophore complexes. These complexes exhibit far-red emission, with high quantum efficiencies and brightness and also exhibit excellent pH stability spanning the range of 2-11. In the course of this study, it became evident that single mutations of L121E and R59W were most effective in improving the fluorescent characteristics of CRABPII mutants as well as the kinetics of complex formation. The readily crystallizable nature of these proteins was invaluable to provide clues for the observed spectroscopic behavior that results from single mutation of key residues. PubMed: 25534273DOI: 10.1021/ja506376j 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.6 Å) |
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