Potent inhibition of HIV-1 fusion by cyanovirin-N requires only a single high affinity carbohydrate binding site: characterization of low affinity carbohydrate binding site knockout mutants (Q38288396)

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English	Potent inhibition of HIV-1 fusion by cyanovirin-N requires only a single high affinity carbohydrate binding site: characterization of low affinity carbohydrate binding site knockout mutants	scientific article

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scholarly article

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Europe PubMed Central

1 September 2017

Potent inhibition of HIV-1 fusion by cyanovirin-N requires only a single high affinity carbohydrate binding site: characterization of low affinity carbohydrate binding site knockout mutants (English)

1 reference

Europe PubMed Central

1 September 2017

author name string

Leng Chee Chang

1

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Europe PubMed Central

1 September 2017

Carole A Bewley

2

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Europe PubMed Central

1 September 2017

language of work or name

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publication date

1 April 2002

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Europe PubMed Central

1 September 2017

Journal of Molecular Biology

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Europe PubMed Central

1 September 2017

318

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Europe PubMed Central

1 September 2017

1

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Europe PubMed Central

1 September 2017

1-8

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Europe PubMed Central

1 September 2017

Multiple antiviral activities of cyanovirin-N: blocking of human immunodeficiency virus type 1 gp120 interaction with CD4 and coreceptor and inhibition of diverse enveloped viruses

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

The potent anti-HIV protein cyanovirin-N contains two novel carbohydrate binding sites that selectively bind to Man(8) D1D3 and Man(9) with nanomolar affinity: implications for binding to the HIV envelope protein gp120.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

HIV entry and its inhibition

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https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

Solution structure of cyanovirin-N, a potent HIV-inactivating protein

1 reference

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7 January 2021

Crystal structure of cyanovirin-N, a potent HIV-inactivating protein, shows unexpected domain swapping

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

Solution structure of a cyanovirin-N:Man alpha 1-2Man alpha complex: structural basis for high-affinity carbohydrate-mediated binding to gp120

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

Measurement of J and dipolar couplings from simplified two-dimensional NMR spectra

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

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Order matrix analysis of residual dipolar couplings using singular value decomposition.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

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Backbone-dependent rotamer library for proteins. Application to side-chain prediction

1 reference

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Sequential CD4-coreceptor interactions in human immunodeficiency virus type 1 Env function: soluble CD4 activates Env for coreceptor-dependent fusion and reveals blocking activities of antibodies against cryptic conserved epitopes on gp120.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

MOLMOL: a program for display and analysis of macromolecular structures

1 reference

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7 January 2021

NMRPipe: a multidimensional spectral processing system based on UNIX pipes

1 reference

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Discovery of cyanovirin-N, a novel human immunodeficiency virus-inactivating protein that binds viral surface envelope glycoprotein gp120: potential applications to microbicide development

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

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Fusogenic mechanisms of enveloped-virus glycoproteins analyzed by a novel recombinant vaccinia virus-based assay quantitating cell fusion-dependent reporter gene activation.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900045-1

7 January 2021

based on heuristic

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10.1016/S0022-2836(02)00045-1

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Europe PubMed Central

1 September 2017

1 reference

Europe PubMed Central

1 September 2017

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