A monomeric mutant of restriction endonuclease EcoRI nicks DNA without sequence specificity
Author:
Publisher
Walter de Gruyter GmbH
Subject
Clinical Biochemistry,Molecular Biology,Biochemistry
Link
https://www.degruyter.com/document/doi/10.1515/BC.2004.127/pdf
Reference28 articles.
1. The influence of sequences adjacent to the recognition site on the cleavage of oligodeoxynucleotides by the EcoRI endonuclease
2. Fluorescence stopped-flow kinetics of the cleavage of synthetic oligodeoxynucleotides by the EcoRI restriction endonuclease
3. Characterization of a novel form of thymidylate synthase: A heterodimer isolated after specific chemical modification of the immobilized native enzyme
4. Sequence-dependent bending propensity of DNA as revealed by DNase I: parameters for trinucleotides.
5. Active site of mercuric reductase resides at the subunit interface and requires Cys135 and Cys140 from one subunit and Cys558 and Cys559 from the adjacent subunit: evidence from in vivo and in vitro heterodimer formation
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Homodimerisation-independent cleavage of dsRNA by a pestiviral nicking endoribonuclease;Scientific Reports;2018-05-29
2. Catalytic Activity Control of Restriction Endonuclease—Triplex Forming Oligonucleotide Conjugates;Bioconjugate Chemistry;2012-01-30
3. The Relationship between Oligomeric State and Protein Function;Advances in Experimental Medicine and Biology;2012
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