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DeepT3 2.0: improving type III secreted effector predictions by an integrative deep learning framework
被引:11
|作者:
Jing, Runyu
[1
,2
]
Wen, Tingke
[1
]
Liao, Chengxiang
[1
]
Xue, Li
[3
]
Liu, Fengjuan
[4
]
Yu, Lezheng
[5
]
Luo, Jiesi
[6
,7
,8
]
机构:
[1] Sichuan Univ, Sch Cyber Sci & Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, Med Big Data Ctr, Chengdu 610065, Peoples R China
[3] Southwest Med Univ, Sch Publ Hlth, Luzhou 646000, Peoples R China
[4] Guizhou Educ Univ, Sch Geog & Resources, Guiyang 550018, Peoples R China
[5] Guizhou Educ Univ, Sch Chem & Mat Sci, Guiyang 550018, Peoples R China
[6] Southwest Med Univ, Dept Pharmacol, Sch Pharm, Luzhou 646000, Peoples R China
[7] Southwest Med Univ, Dept Pharm, Affiliated Hosp, Luzhou 646000, Peoples R China
[8] Southwest Med Univ, Sichuan Key Med Lab New Drug Discovery & Druggabi, Luzhou Key Lab Act Screening & Druggabil Evaluat, Luzhou 646000, Peoples R China
基金:
中国国家自然科学基金;
关键词:
COMPUTATIONAL PREDICTION;
SYSTEMS;
PROTEINS;
IV;
ARCHITECTURE;
MECHANISMS;
SERVER;
EXPORT;
D O I:
10.1093/nargab/lqab086
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Type III secretion systems (T3SSs) are bacterial membrane-embedded nanomachines that allow a number of humans, plant and animal pathogens to inject virulence factors directly into the cytoplasm of eukaryotic cells. Export of effectors through T3SSs is critical for motility and virulence of most Gram-negative pathogens. Current computational methods can predict type Ill secreted effectors (T3SEs) from amino acid sequences, but due to algorithmic constraints, reliable and large-scale prediction of T3SEs in Gram-negative bacteria remains a challenge. Here, we present DeepT3 2.0 (http://advintbioinforlab.com/deept3/), a novel web server that integrates different deep learning models for genome-wide predicting T3SEs from a bacterium of interest. DeepT3 2.0 combines various deep learning architectures including convolutional, recurrent, convolutional-recurrent and multilayer neural networks to learn N-terminal representations of proteins specifically for T3SE prediction. Outcomes from the different models are processed and integrated for discriminating T3SEs and non-T3SEs. Because it leverages diverse models and an integrative deep learning framework, DeepT3 2.0 outperforms existing methods in validation datasets. In addition, the features learned from networks are analyzed and visualized to explain how models make their predictions. We propose DeepT3 2.0 as an integrated and accurate tool for the discovery of T3SEs.
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页数:14
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