1wp5: Difference between revisions
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New page: left|200px<br /><applet load="1wp5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1wp5, resolution 1.79Å" /> '''Crystal structure of... |
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[[Image:1wp5.gif|left|200px]]<br /><applet load="1wp5" size=" | [[Image:1wp5.gif|left|200px]]<br /><applet load="1wp5" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1wp5, resolution 1.79Å" /> | caption="1wp5, resolution 1.79Å" /> | ||
'''Crystal structure of the C-terminal domain of DNA topoisomerase IV'''<br /> | '''Crystal structure of the C-terminal domain of DNA topoisomerase IV'''<br /> | ||
==Overview== | ==Overview== | ||
Bacteria possess two closely related yet functionally distinct essential | Bacteria possess two closely related yet functionally distinct essential type IIA topoisomerases (Topos). DNA gyrase supports replication and transcription with its unique supercoiling activity, whereas Topo IV preferentially relaxes (+) supercoils and is a decatenating enzyme required for chromosome segregation. Here we report the crystal structure of the C-terminal domain of Topo IV ParC subunit (ParC-CTD) from Bacillus stearothermophilus and provide a structure-based explanation for how Topo IV and DNA gyrase execute distinct activities. Although the topological connectivity of ParC-CTD is similar to the recently determined CTD structure of DNA gyrase GyrA subunit (GyrA-CTD), ParC-CTD surprisingly folds as a previously unseen broken form of a six-bladed beta-propeller. Propeller breakage is due to the absence of a DNA gyrase-specific GyrA box motif, resulting in the reduction of curvature of the proposed DNA binding region, which explains why ParC-CTD is less efficient than GyrA-CTD in mediating DNA bending, a difference that leads to divergent activities of the two homologous enzymes. Moreover, we found that the topology of the propeller blades observed in ParC-CTD and GyrA-CTD can be achieved from a concerted beta-hairpin invasion-induced fold change event of a canonical six-bladed beta-propeller; hence, we proposed to name this new fold as "hairpin-invaded beta-propeller" to highlight the high degree of similarity and a potential evolutionary linkage between them. The possible role of ParC-CTD as a geometry facilitator during various catalytic events and the evolutionary relationships between prokaryotic type IIA Topos have also been discussed according to these new structural insights. | ||
==About this Structure== | ==About this Structure== | ||
1WP5 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus]. Full crystallographic information is available from [http:// | 1WP5 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WP5 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Geobacillus stearothermophilus]] | [[Category: Geobacillus stearothermophilus]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
[[Category: Chan, N | [[Category: Chan, N L.]] | ||
[[Category: Farh, L.]] | [[Category: Farh, L.]] | ||
[[Category: Hsieh, T | [[Category: Hsieh, T J.]] | ||
[[Category: Huang, W | [[Category: Huang, W M.]] | ||
[[Category: broken beta-propeller]] | [[Category: broken beta-propeller]] | ||
[[Category: hairpin-invaded beta-propeller]] | [[Category: hairpin-invaded beta-propeller]] | ||
[[Category: six-bladed beta-propeller]] | [[Category: six-bladed beta-propeller]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:46:47 2008'' | ||