ZHAO Xin Min; XIA Li Qiu; YANG Xiao Ping; PENG Xiao Yun

doi:10.3967/bes2015.089

Flexibility Analysis of Bacillus thuringiensis Cry1Aa

ZHAO Xin Min, XIA Li Qiu, YANG Xiao Ping, PENG Xiao Yun

文章导航 > Biomedical and Environmental Sciences > 2015 > 28(9): 634-641

ZHAO Xin Min, XIA Li Qiu, YANG Xiao Ping, PENG Xiao Yun. Flexibility Analysis of Bacillus thuringiensis Cry1Aa[J]. Biomedical and Environmental Sciences, 2015, 28(9): 634-641. doi: 10.3967/bes2015.089

Citation:

ZHAO Xin Min, XIA Li Qiu, YANG Xiao Ping, PENG Xiao Yun. Flexibility Analysis of Bacillus thuringiensis Cry1Aa[J]. Biomedical and Environmental Sciences, 2015, 28(9): 634-641. doi: 10.3967/bes2015.089

doi: 10.3967/bes2015.089

基金项目: This study was supported by grants from the National Natural Science Foundation of China(30670052)%863 Program of China(2006AA02Z187)

Flexibility Analysis of Bacillus thuringiensis Cry1Aa

Department of Chemistry and Environmental Engineering, Hunan City University, Yiyang 413000, Hunan, China
Key Laboratory of Microbial Molecular Biology of Hunan Province, College of Life Science, Hunan Normal University, Changsha 410081, Hunan, China

Funds: This study was supported by grants from the National Natural Science Foundation of China(30670052)%863 Program of China(2006AA02Z187)

摘要: Objective To investigate the flexibility and mobility of the Bacillus thuringiensis toxin Cry1Aa.
Methods The graph theory-based program Constraint Network Analysis and normal mode-based program NMsim were used to analyze the global and local flexibility indices as well as the fluctuation of individual residues in detail.
Results The decrease in Cry1Aa network rigidity with the increase of temperature was evident. Two phase transition points in which the Cry1Aa structure lost rigidity during the thermal simulation were identified. Two rigid clusters were found in domains I and II. Weak spots were found in C-terminal domain III. Several flexible regions were found in all three domains;the largest residue fluctuation was present in the apical loop2 of domain II.
Conclusion Although several flexible regions could be found in all the three domains, the most flexible regions were in the apical loops of domain II.
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Abstract: Objective To investigate the flexibility and mobility of the Bacillus thuringiensis toxin Cry1Aa.
Methods The graph theory-based program Constraint Network Analysis and normal mode-based program NMsim were used to analyze the global and local flexibility indices as well as the fluctuation of individual residues in detail.
Results The decrease in Cry1Aa network rigidity with the increase of temperature was evident. Two phase transition points in which the Cry1Aa structure lost rigidity during the thermal simulation were identified. Two rigid clusters were found in domains I and II. Weak spots were found in C-terminal domain III. Several flexible regions were found in all three domains;the largest residue fluctuation was present in the apical loop2 of domain II.
Conclusion Although several flexible regions could be found in all the three domains, the most flexible regions were in the apical loops of domain II.
- Flexibility /
- Cry1Aa /
- Bacillus thuringiensis /
- Constraint Network Analysis /
- NMSim

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Flexibility Analysis of Bacillus thuringiensis Cry1Aa

doi: 10.3967/bes2015.089

基金项目: This study was supported by grants from the National Natural Science Foundation of China(30670052)%863 Program of China(2006AA02Z187)

刊出日期: 2015-09-20

关键词:

Flexibility /

Cry1Aa /

Bacillus thuringiensis /

Constraint Network Analysis /

NMSim

摘要: Objective To investigate the flexibility and mobility of the Bacillus thuringiensis toxin Cry1Aa.
Methods The graph theory-based program Constraint Network Analysis and normal mode-based program NMsim were used to analyze the global and local flexibility indices as well as the fluctuation of individual residues in detail.
Results The decrease in Cry1Aa network rigidity with the increase of temperature was evident. Two phase transition points in which the Cry1Aa structure lost rigidity during the thermal simulation were identified. Two rigid clusters were found in domains I and II. Weak spots were found in C-terminal domain III. Several flexible regions were found in all three domains;the largest residue fluctuation was present in the apical loop2 of domain II.
Conclusion Although several flexible regions could be found in all the three domains, the most flexible regions were in the apical loops of domain II.