Structural Basis of Covalent Inhibitory Mechanism of TMPRSS2-Related Serine Proteases by Camostat
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- Gaohui Sun
- College of Chemistry, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Yaqun Sui
- College of Chemistry, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Yang Zhou
- College of Chemistry, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Junlin Ya
- College of Chemistry, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Cai Yuan
- College of Biological Science and Engineering, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Longguang Jiang
- College of Chemistry, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Mingdong Huang
- College of Chemistry, Fuzhou University, Fuzhou, Fujian, People’s Republic of China
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- Rebecca Ellis Dutch
- editor
書誌事項
- 公開日
- 2021-09-09
- 権利情報
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- https://doi.org/10.1128/ASMCopyrightv2
- https://journals.asm.org/non-commercial-tdm-license
- DOI
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- 10.1128/jvi.00861-21
- 公開者
- American Society for Microbiology
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説明
<jats:p>Serine proteases are a large family of enzymes critical for multiple physiological processes and proven diagnostic and therapeutic targets in several clinical indications. The serine protease transmembrane protease serine 2 (TMPRSS2) was recently found to mediate SARS-CoV-2 entry into the host.</jats:p>
収録刊行物
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- Journal of Virology
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Journal of Virology 95 (19), e00861-21-, 2021-09-09
American Society for Microbiology