Recent Advances in β-Strand Mimetics - Wikidata - awgldk - TriplyDB

Recent Advances in β-Strand Mimetics

Recent Advances in β-Strand Mimetics

http://www.wikidata.org/entity/Q57080840

about

Extension of the CHARMM General Force Field to sulfonyl-containing compounds and its utility in biomolecular simulations.

P2860

Q34347574-80F1BA9A-E313-4BBF-813B-5794B17F9C2B

P2860

Recent Advances in β-Strand Mimetics

http://www.wikidata.org/entity/Q57080840

description

wetenschappelijk artikel

@nl

наукова стаття, опублікована у квітні 2011

@uk

name

Recent Advances in β-Strand Mimetics

@en

Recent Advances in β-Strand Mimetics

@nl

type

label

Recent Advances in β-Strand Mimetics

@en

Recent Advances in β-Strand Mimetics

@nl

prefLabel

Recent Advances in β-Strand Mimetics

@en

Recent Advances in β-Strand Mimetics

@nl

P1476

Q57080840-0224DF86-77BE-405C-87A1-AF50D8EFAF04

P2093

Q57080840-2F9760C5-1699-4A72-ADD6-8239B4123716

Q57080840-3276F28C-27D4-4075-BD74-B5426D7808E8

P2860

Q57080840-142EEAD5-2797-4542-88AA-E88A672E6147

Q57080840-1B8907F5-6124-47DD-8D04-15B0E998ECC5

Q57080840-1E53DCCF-2A9E-4BB2-B0BC-6F81023CA4EB

Q57080840-1E85F38D-3D8D-4C07-BF97-6FE573D1D251

Q57080840-1F65867C-B344-4588-8675-5770E9CD5F53

Q57080840-24E02A10-8118-4B45-8ADA-8D816B3EFB12

Q57080840-2733A2AC-641E-4EAB-B65F-EFEB7F8B3531

Q57080840-2C68195C-6CCF-414D-BC16-73C45094AFB5

Q57080840-2F55A319-BB1A-4C84-B55C-6EE9CE0FFBBE

Q57080840-316DD9D9-D53E-42B8-9F84-A674AB4AB23A

P304

Q57080840-35D2EA87-ABD4-423E-8C9E-68B111E04111

P31

Q57080840-F42905ED-FB80-4FFF-93BD-366C6CA8726A

P356

Q57080840-840595AC-8952-40DF-BB7A-7E2938A9E004

P577

Q57080840-DBFF0033-C97A-4CBB-9E8E-0534B4ED50CA

P356

9783527631827.CH3

P1476

Recent Advances in β-Strand Mimetics

@en

P2093

David P. Fairlie

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

Wendy A. Loughlin

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

P2860

Molecular recognition of macrocyclic peptidomimetic inhibitors by HIV-1 protease

Synthesis, stability, antiviral activity, and protease-bound structures of substrate-mimicking constrained macrocyclic inhibitors of HIV-1 protease

Crystal structures of highly constrained substrate and hydrolysis products bound to HIV-1 protease. Implications for the catalytic mechanism

Structure-based design of novel HIV protease inhibitors: carboxamide-containing 4-hydroxycoumarins and 4-hydroxy-2-pyrones as potent nonpeptidic inhibitors

Crystal structure of a TFIIB-TBP-TATA-element ternary complex

Protein misfolding, functional amyloid, and human disease

Molecular Recognition of Protein−Ligand Complexes: Applications to Drug Design

Proteases universally recognize beta strands in their active sites

Protease inhibitors: current status and future prospects

Conformational selection of inhibitors and substrates by proteolytic enzymes: implications for drug design and polypeptide processing

P304

129-147

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

P31

scholarly article

P356

10.1002/9783527631827.CH3

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

P577

2011-04-07T00:00:00Z

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