Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction - Test2 - elhamkhani - TriplyDB

Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction

Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction

http://www.wikidata.org/entity/Q27689051

about

Spacer-free BODIPY fluorogens in antimicrobial peptides for direct imaging of fungal infection in human tissue Double Strain-Promoted Macrocyclization for the Rapid Selection of Cell-Active Stapled Peptides Constraining an Irregular Peptide Secondary Structure through Ring-Closing Alkyne Metathesis Characterization of Promiscuous Binding of Phosphor Ligands to Breast-Cancer-Gene 1 (BRCA1) C-Terminal (BRCT): Molecular Dynamics, Free Energy, Entropy and Inhibitor Design β-Turn mimetic-based stabilizers of protein-protein interactions for the study of the non-canonical roles of leucyl-tRNA synthetase.Small molecules, peptides and natural products: getting a grip on 14-3-3 protein-protein modulation.EMBO conference series: Chemical Biology 2014 Targeting protein-protein interfaces using macrocyclic peptides.Protein-protein interactions as drug targets.Stapled Peptides with γ-Methylated Hydrocarbon Chains for the Estrogen Receptor/Coactivator Interaction.Macrocyclized Extended Peptides: Inhibiting the Substrate-Recognition Domain of Tankyrase.New Modalities for Challenging Targets in Drug Discovery.Modulating protein-protein interactions: the potential of peptides.Structure-Based Design of Inhibitors of Protein-Protein Interactions: Mimicking Peptide Binding Epitopes.A Blind Test of Computational Technique for Predicting the Likelihood of Peptide Sequences to Cyclize.Targeting recognition surfaces on natural proteins with peptidic foldamers Peptides and peptidomimetics as regulators of protein-protein interactions.Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides.Identification of Two Secondary Ligand Binding Sites in 14-3-3 Proteins Using Fragment Screening.A Binary Bivalent Supramolecular Assembly Platform Based on Cucurbit[8]uril and Dimeric Adapter Protein 14-3-3.A Synthetic Loop Replacement Peptide That Blocks Canonical NF-κB Signaling.Structure-Based Design of Non-natural Macrocyclic Peptides That Inhibit Protein-Protein Interactions.Thermodynamic origin of α-helix stabilization by side-chain cross-links in a small protein.Increased Conformational Flexibility of a Macrocycle-Receptor Complex Contributes to Reduced Dissociation Rates.Turning a Substrate Peptide into a Potent Inhibitor for the Histone Methyltransferase SETD8.Preparation of tri(ethylene glycol) grafted core-shell type polymer support for solid-phase peptide synthesis.Bcl-XL-binding helical peptides possessing d-Ala residues at their C-termini with the advantage of long-lasting intracellular stabilities.Modulators of 14-3-3 Protein-Protein Interactions.Peptide Macrocycles Developed from Precisely Regulated Multiple Cyclization of Unprotected Peptides.General and Facile Route to Isomerically Pure Tricyclic Peptides Based on Templated Tandem CLIPS/CuAAC Cyclizations.Stabilization of peptides against proteolysis through disulfide-bridged conjugation with synthetic aromatics.Precisely Regulated and Efficient Locking of Linear Peptides into Stable Multicyclic Topologies through a One-Pot Reaction.Identification of Inhibitors of Pseudomonas aeruginosa Exotoxin-S ADP-Ribosyltransferase Activity.Constructing thioether-tethered cyclic peptides via on-resin intra-molecular thiol-ene reaction.Protease-Activatable Scaffold Proteins as Versatile Molecular Hubs in Synthetic Signaling Networks A Binary Bivalent Supramolecular Assembly Platform Based on Cucurbit[8]uril and Dimeric Adapter Protein 14-3-3 Model foldamers: applications and structures of stable macrocyclic peptides identified using in vitro selection 14-3-3 proteins activate Pseudomonas exotoxins-S and -T by chaperoning a hydrophobic surface

P2860

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P2860

Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction

http://www.wikidata.org/entity/Q27689051

description

2014 nî lūn-bûn

@nan

2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Constrained peptides with targ ...... ic protein-protein interaction

@ast

Constrained peptides with targ ...... ic protein-protein interaction

@en

Constrained peptides with targ ...... ic protein-protein interaction

@nl

type

label

Constrained peptides with targ ...... ic protein-protein interaction

@ast

Constrained peptides with targ ...... ic protein-protein interaction

@en

Constrained peptides with targ ...... ic protein-protein interaction

@nl

prefLabel

Constrained peptides with targ ...... ic protein-protein interaction

@ast

Constrained peptides with targ ...... ic protein-protein interaction

@en

Constrained peptides with targ ...... ic protein-protein interaction

@nl

P1433

Q27689051-EEFCF1EF-D76A-4367-BB20-0D757E0ADA32

P1476

Q27689051-B6863AFF-C046-434B-AF6A-113F1069E9A4

P2093

Q27689051-3151C8F6-170C-4235-9C8C-513A33E80CCE

Q27689051-6156E1DF-4015-44FE-B990-A012BA723DE2

Q27689051-9F6C87DF-D18E-4C15-82E9-80446EDA4228

Q27689051-D50C6B52-14B2-4980-BE62-D7328498838E

P2860

Q27689051-1EFC872B-A801-4F0F-A4FC-1F5A1323A80A

Q27689051-1F3DF067-3137-422B-9C23-99E3360DE4AC

Q27689051-2A9E6F36-91A1-40A7-B810-4BFAED4E1588

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Q27689051-7A59AD1F-8589-427E-AE0F-B62353681BE9

Q27689051-84A6FB9C-CA15-46AF-9999-764AFBA39844

Q27689051-84BCD5B9-AB36-47CE-A2B0-F55AB4E3BEB7

P304

Q27689051-1FED33D1-60F2-402A-8613-FB4A1D9DD2C6

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Q27689051-BE1608A6-77FC-499D-8FFD-700798715A16

P3181

Q27689051-732F91A1-0D97-400B-B4A5-1FD09D2466D0

P356

Q27689051-DAD497DA-3950-4752-9997-F9B03AAC3B8F

P407

Q27689051-06182D02-C320-4A93-B5BF-EADA617D55D1

P433

Q27689051-7D6ADD71-DC02-4AE6-8AF6-0BF94786AD1A

P478

Q27689051-D8F13892-46DD-4888-9A91-469AC354100E

P50

Q27689051-15637B2D-1648-4C52-B52E-4E3E4F8D2925

Q27689051-199EB2E6-715B-4FB5-94DD-1B97C6E7BC5C

P577

Q27689051-6656CFC5-2322-44FA-AD2E-BCD519BB7C10

P698

Q27689051-AA844670-2BDD-4B2E-8D0C-A3F506C0FAF3

P3181

P356

P1433

Angewandte Chemie International Edition

P1476

Constrained peptides with targ ...... ic protein-protein interaction

@en

P2093

Adrian Glas

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

David Bier

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

Gernot Hahne

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

Tom N Grossmann

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

P2860

Phosphorylation-independent interaction between 14-3-3 and exoenzyme S: from structure to pathogenesis

The MCL-1 BH3 helix is an exclusive MCL-1 inhibitor and apoptosis sensitizer

Design and structure of stapled peptides binding to estrogen receptors

Structure of the stapled p53 peptide bound to Mdm2

Bicyclic peptide inhibitor reveals large contact interface with a protease target

Stapled α−helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy

Peptidomimetic antibiotics target outer-membrane biogenesis in Pseudomonas aeruginosa

Can self-inhibitory peptides be derived from the interfaces of globular protein-protein interactions?

Beta-hairpin peptidomimetics: design, structures and biological activities.

NMR screening and crystal quality of bacterially expressed prokaryotic and eukaryotic proteins in a structural genomics pipeline

P304

2489-93

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P31

scholarly article

P3181

3893729

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P356

10.1002/ANIE.201310082

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P407

P433

9

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P478

53

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P50

Christian Ottmann

Christoph Rademacher

P577

2014-02-24T00:00:00Z

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P698

24504455

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