Multi-target Fragments Display Versatile Binding Modes.

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Multi-target Fragments Display Versatile Binding Modes.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Multi-target Fragments Display Versatile Binding Modes.

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Multi-target Fragments Display Versatile Binding Modes.

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Multi-target Fragments Display Versatile Binding Modes.

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Multi-target Fragments Display Versatile Binding Modes.

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Multi-target Fragments Display Versatile Binding Modes.

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Multi-target Fragments Display Versatile Binding Modes.

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P1476

Multi-target Fragments Display Versatile Binding Modes.

@en

P2093

Guillaume Bret

http://www.w3.org/2001/XMLSchema#string

Malgorzata N Drwal

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P2860

The Protein Data Bank

BindingDB: a web-accessible database of experimentally determined protein-ligand binding affinities

EMBOSS: the European Molecular Biology Open Software Suite

Protein structure alignment by incremental combinatorial extension (CE) of the optimal path

Identification and selection of "privileged fragments" suitable for primary screening.

Lessons for fragment library design: analysis of output from multiple screening campaigns.

Ligand specificity, privileged substructures and protein druggability from fragment-based screening.

Thermodynamics of fragment binding.

Design Principles for Fragment Libraries: Maximizing the Value of Learnings from Pharma Fragment-Based Drug Discovery (FBDD) Programs for Use in Academia.

Twenty years on: the impact of fragments on drug discovery.

P31

scholarly article

P356

10.1002/MINF.201700042

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Esther Kellenberger

P577

2017-07-10T00:00:00Z

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P698

28691374

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