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1XSS

Semi-rational engineering of a green-emitting coral fluorescent protein into an efficient highlighter.

1XSS の概要
エントリーDOI10.2210/pdb1xss/pdb
分子名称fluorescent protein, MAGNESIUM ION, SODIUM ION, ... (4 entities in total)
機能のキーワードfluorescent protein, luminescent protein
由来する生物種Favia favus
タンパク質・核酸の鎖数2
化学式量合計51817.65
構造登録者
Tsutsui, H.,Karasawa, S.,Shimizu, H.,Nukina, N.,Miyawaki, A. (登録日: 2004-10-20, 公開日: 2005-03-15, 最終更新日: 2026-03-18)
主引用文献Tsutsui, H.,Karasawa, S.,Shimizu, H.,Nukina, N.,Miyawaki, A.
Semi-rational engineering of a coral fluorescent protein into an efficient highlighter
Embo Rep., 6:233-238, 2005
Cited by
PubMed Abstract: Kaede is a natural photoconvertible fluorescent protein found in the coral Trachyphyllia geoffroyi. It contains a tripeptide, His 62-Tyr 63-Gly 64, which acts as a green chromophore that is photoconvertible to red following (ultra-) violet irradiation. Here, we report the molecular cloning and crystal structure determination of a new fluorescent protein, KikG, from the coral Favia favus, and its in vitro evolution conferring green-to-red photoconvertibility. Substitution of the His 62-Tyr 63-Gly 64 sequence into the native protein provided only negligible photoconversion. On the basis of the crystal structure, semi-rational mutagenesis of the amino acids surrounding the chromophore was performed, leading to the generation of an efficient highlighter, KikGR. Within mammalian cells, KikGR is more efficiently photoconverted and is several-fold brighter in both the green and red states than Kaede. In addition, KikGR was successfully photoconverted using two-photon excitation microscopy at 760 nm, ensuring optical cell labelling with better spatial discrimination in thick and highly scattering tissues.
PubMed: 15731765
DOI: 10.1038/sj.embor.7400361
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.6 Å)
構造検証レポート
Validation report summary of 1xss
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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