DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) complex / DNA negative supercoiling activity / DNA topoisomerase (ATP-hydrolysing) / DNA topological change / DNA-templated DNA replication / chromosome / response to antibiotic / DNA binding / ATP binding / metal ion binding / cytoplasm 類似検索 - 分子機能
Topoisomerase II; domain 5 / Topoisomerase II, domain 5 / Topoisomerase, domain 3 / Topoisomerase; domain 3 / Rossmann fold - #670 / Gyrase A; domain 2 - #40 / DNA gyrase, subunit A / DNA gyrase/topoisomerase IV, subunit A, C-terminal repeat / DNA gyrase/topoisomerase IV, subunit A, C-terminal / : ...Topoisomerase II; domain 5 / Topoisomerase II, domain 5 / Topoisomerase, domain 3 / Topoisomerase; domain 3 / Rossmann fold - #670 / Gyrase A; domain 2 - #40 / DNA gyrase, subunit A / DNA gyrase/topoisomerase IV, subunit A, C-terminal repeat / DNA gyrase/topoisomerase IV, subunit A, C-terminal / : / DNA gyrase C-terminal domain, beta-propeller / DNA gyrase subunit B, TOPRIM domain / DNA gyrase, subunit B / DNA topoisomerase, type IIA, subunit B / DNA gyrase B subunit, C-terminal / DNA gyrase B subunit, carboxyl terminus / Topoisomerase (Topo) IIA-type catalytic domain profile. / DNA topoisomerase, type IIA, alpha-helical domain superfamily / DNA topoisomerase, type IIA, domain A / DNA topoisomerase, type IIA, domain A, alpha-beta / DNA gyrase/topoisomerase IV, subunit A / DNA Topoisomerase IV / DNA topoisomerase, type IIA, subunit B, domain 2 / DNA gyrase B / DNA topoisomerase, type IIA / DNA topoisomerase, type IIA, conserved site / DNA topoisomerase II signature. / TopoisomeraseII / DNA topoisomerase, type IIA, subunit B, C-terminal / Toprim domain / DNA topoisomerase, type IIA-like domain superfamily / Toprim domain profile. / TOPRIM domain / Gyrase A; domain 2 / Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase / Histidine kinase-like ATPases / Histidine kinase/HSP90-like ATPase superfamily / Ribosomal protein S5 domain 2-type fold, subgroup / Ribosomal protein S5 domain 2-type fold / Alpha-Beta Complex / Rossmann fold / 2-Layer Sandwich / Orthogonal Bundle / 3-Layer(aba) Sandwich / Mainly Alpha / Alpha Beta 類似検索 - ドメイン・相同性
Chem-RXV / DNA / DNA (> 10) / DNA gyrase subunit B / DNA gyrase subunit A 類似検索 - 構成要素
#241 - 2020年1月 20年の分子を振り返って (Twenty Years of Molecules) 類似性 (1)
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集合体
登録構造単位
B: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A D: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A E: 5'-D(*5UA*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' F: 5'-D(*5UA*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' S: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A U: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A V: 5'-D(*AP*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' W: 5'-D(*AP*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' ヘテロ分子
B: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A D: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A E: 5'-D(*5UA*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' F: 5'-D(*5UA*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' ヘテロ分子
S: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A U: DNA GYRASE SUBUNIT B, DNA GYRASE SUBUNIT A V: 5'-D(*AP*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' W: 5'-D(*AP*GP*CP*CP*GP*TP*AP*GP*GP*GP*CP*CP*CP*TP*AP*CP*GP *GP*CP*TP)-3' ヘテロ分子
ENGINEERED RESIDUE IN CHAIN B, TYR 123 TO PHE ENGINEERED RESIDUE IN CHAIN D, TYR 123 TO PHE ...ENGINEERED RESIDUE IN CHAIN B, TYR 123 TO PHE ENGINEERED RESIDUE IN CHAIN D, TYR 123 TO PHE ENGINEERED RESIDUE IN CHAIN S, TYR 123 TO PHE ENGINEERED RESIDUE IN CHAIN U, TYR 123 TO PHE
非ポリマーの詳細
ACETYLATED ADENOSINE : IN HIGHER RESOLUTION 2.1A STRUCTURE WAS EXTRA DENSITY ON ONE END OF DNA, ...ACETYLATED ADENOSINE : IN HIGHER RESOLUTION 2.1A STRUCTURE WAS EXTRA DENSITY ON ONE END OF DNA, MODELLED AS ACETYLATED ADENOSINE.
配列の詳細
THIS IS A FUSION TRUNCATE IN WHICH THE C-TERMINAL RESIDUE OF GYRB (F644) IS FUSED TO THE N-TERMINAL ...THIS IS A FUSION TRUNCATE IN WHICH THE C-TERMINAL RESIDUE OF GYRB (F644) IS FUSED TO THE N-TERMINAL RESIDUE OF GYRA (A2). CATALYTIC TYROSINE (123) HAS BEEN MUTATED TO PHENYLALANINE