(Q34390896)

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Molecular modeling and chemical modification for finding peptide inhibitor against severe acute respiratory syndrome coronavirus main proteinase

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scholarly article

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Europe PubMed Central

PubMed publication ID

1 August 2017

Molecular modeling and chemical modification for finding peptide inhibitor against severe acute respiratory syndrome coronavirus main proteinase (English)

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Europe PubMed Central

PubMed publication ID

1 August 2017

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Kuo-Chen Chou

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1 August 2017

author name string

Qishi Du

1

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Europe PubMed Central

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1 August 2017

Shuqing Wang

2

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1 August 2017

Dongqing Wei

3

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1 August 2017

Suzanne Sirois

4

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1 August 2017

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publication date

1 February 2005

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1 August 2017

Analytical Biochemistry

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1 August 2017

337

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1 August 2017

2

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Europe PubMed Central

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1 August 2017

262-270

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Europe PubMed Central

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1 August 2017

H-77: a potent new renin inhibitor. In vitro and in vivo studies.

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Severe acute respiratory syndrome and influenza: virus incursions from southern China

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Prediction of proteinase cleavage sites in polyproteins of coronaviruses and its applications in analyzing SARS-CoV genomes.

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Virtual screening for SARS-CoV protease based on KZ7088 pharmacophore points

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Coronavirus main proteinase (3CLpro) structure: basis for design of anti-SARS drugs

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A computational procedure for determining energetically favorable binding sites on biologically important macromolecules

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Functionality maps of binding sites: a multiple copy simultaneous search method

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Solution structure of the RAIDD CARD and model for CARD/CARD interaction in caspase-2 and caspase-9 recruitment

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Binding mechanism of coronavirus main proteinase with ligands and its implication to drug design against SARS.

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Identification of the N-terminal functional domains of Cdk5 by molecular truncation and computer modeling

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Prediction of the tertiary structure of the beta-secretase zymogen

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Prediction of the tertiary structure of a caspase-9/inhibitor complex

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A vectorized sequence-coupling model for predicting HIV protease cleavage sites in proteins.

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N-terminal domain of the murine coronavirus receptor CEACAM1 is responsible for fusogenic activation and conformational changes of the spike protein

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Converting a peptide into a drug: strategies to improve stability and bioavailability

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Identifiers

10.1016/J.AB.2004.10.003

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

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