5ESP

Crystal Structure of LAGLIDADG Meganuclease I-PanMI with coordinated Calcium ions

5ESP の概要

• エントリーDOI: 10.2210/pdb5esp/pdb
• 分子名称: I-PanMI, DNA (27-MER), CALCIUM ION, ... (6 entities in total)
• 機能のキーワード: hydrolase-dna complex, laglidadg, homing endonuclease, meganuclease, hydrolase/dna
• 由来する生物種: Podospora anserina (Pleurage anserina); 詳細
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 101523.20

構造登録者

Hallinan, J.P.,Stoddard, B.L. (登録日: 2015-11-16, 公開日: 2016-03-30, 最終更新日: 2024-03-13)

主引用文献

Lambert, A.R.,Hallinan, J.P.,Shen, B.W.,Chik, J.K.,Bolduc, J.M.,Kulshina, N.,Robins, L.I.,Kaiser, B.K.,Jarjour, J.,Havens, K.,Scharenberg, A.M.,Stoddard, B.L.
Indirect DNA Sequence Recognition and Its Impact on Nuclease Cleavage Activity.
Structure, 24:862-873, 2016

PubMed Abstract: LAGLIDADG meganucleases are DNA cleaving enzymes used for genome engineering. While their cleavage specificity can be altered using several protein engineering and selection strategies, their overall targetability is limited by highly specific indirect recognition of the central four base pairs within their recognition sites. In order to examine the physical basis of indirect sequence recognition and to expand the number of such nucleases available for genome engineering, we have determined the target sites, DNA-bound structures, and central four cleavage fidelities of nine related enzymes. Subsequent crystallographic analyses of a meganuclease bound to two noncleavable target sites, each containing a single inactivating base pair substitution at its center, indicates that a localized slip of the mutated base pair causes a small change in the DNA backbone conformation that results in a loss of metal occupancy at one binding site, eliminating cleavage activity.

PubMed: 27133026
DOI: 10.1016/j.str.2016.03.024

実験手法

X-RAY DIFFRACTION (2.995 Å)