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Predict the strong binding ability polypeptide of human α-enolase with the HLA-DRB1 * 0401

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成果类型:
期刊论文、会议论文
作者:
Jie, Rui;Zhou, Quan;Wang, Jin Song;Liang, Yun He;Liao, Ting Ting;...
通讯作者:
Geng, H.(genghui@mail.ccnu.edu.cn)
作者机构:
[Yu, Jin Hui; Liu, De Li; Liao, Ting Ting; Zhou, Quan; Wang, Jin Song; Geng, Hui; Jie, Rui; Liang, Yun He] Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Science, Central China Normal University, Wuhan 430079, China
通讯机构:
[Geng, H.] H
Hubei Key Laboratory of Genetic Regulation and Integrative Biology, , Wuhan 430079, China
语种:
英文
关键词:
Epitope predition;Human α-enolase;Ligand binding;Molecular modeling
期刊:
Applied Mechanics and Materials
ISSN:
1660-9336
年:
2013
卷:
380-384
页码:
4353-4358
会议名称:
2013 International Conference on Vehicle and Mechanical Engineering and Information Technology, VMEIT 2013
会议时间:
17 August 2013 through 18 August 2013
ISBN:
9783037858202
机构署名:
本校为第一机构
院系归属:
生命科学学院
摘要:
Human α-enolase (ENO1), an evolutionarily conserved and multifunctional protein, is a target self-antigen of rheumatoid arthritis (RA). Rheumatoid arthritis (RA) is genetically associated with MHC class II molecules, such as DRB1*0101, DRB1*0401 and DRB1*0404 allele. Among these DRB1 alleles, DRB1*0401 show the most correlation with RA. However, strong binding ability polypeptide of ENO1 with HLA-DRB1*0401 is still largely unknown. In this study, we used NetMHCII prediction method to predict the strong binding ability polypeptide with HLADRB1* 0401. Among the 434 predicted fragment pepti...

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