Sequence Determinants of a Specific Inactive Protein Kinase Conformation - Wikidata - wikimedia - TriplyDB

Sequence Determinants of a Specific Inactive Protein Kinase Conformation

Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Targeting cancer with kinase inhibitors Exploration of type II binding mode: A privileged approach for kinase inhibitor focused drug discovery?Molecular dynamics of PLK1 during mitosis A Highly Selective Dual Insulin Receptor (IR)/Insulin-like Growth Factor 1 Receptor (IGF-1R) Inhibitor Derived from an Extracellular Signal-regulated Kinase (ERK) Inhibitor Conformation-Selective ATP-Competitive Inhibitors Control Regulatory Interactions and Noncatalytic Functions of Mitogen-Activated Protein Kinases Structure of a pathogen effector reveals the enzymatic mechanism of a novel acetyltransferase family Structure-guided selection of specificity determining positions in the human Kinome DFGmodel: predicting protein kinase structures in inactive states for structure-based discovery of type-II inhibitors Conformational analysis of the DFG-out kinase motif and biochemical profiling of structurally validated type II inhibitors.Slow inhibition and conformation selective properties of extracellular signal-regulated kinase 1 and 2 inhibitors A unique inhibitor binding site in ERK1/2 is associated with slow binding kinetics.From Type I to Type II: Design, Synthesis, and Characterization of Potent Pyrazin-2-ones as DFG-Out Inhibitors of PDGFRβ.Tropomyosin receptor kinase inhibitors: an updated patent review for 2010-2016 - Part I.Gatekeeper Tyrosine Phosphorylation of SYMRK Is Essential for Synchronizing the Epidermal and Cortical Responses in Root Nodule Symbiosis.Structural Insight into the 14-3-3 Protein-dependent Inhibition of Protein Kinase ASK1 (Apoptosis Signal-regulating kinase 1).Trans-membrane Signaling in Photosynthetic State Transitions: REDOX- AND STRUCTURE-DEPENDENT INTERACTION IN VITRO BETWEEN STT7 KINASE AND THE CYTOCHROME b6f COMPLEX.Conformation-selective inhibitors reveal differences in the activation and phosphate-binding loops of the tyrosine kinases Abl and Src.Structural and dynamic insights into the energetics of activation loop rearrangement in FGFR1 kinase.Structure of PINK1 and mechanisms of Parkinson's disease-associated mutations.A Comprehensive Structural Overview of p38α Mitogen-Activated Protein Kinase in Complex with ATP-Site and Non-ATP-Site Binders.

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P2860

Sequence Determinants of a Specific Inactive Protein Kinase Conformation

http://www.wikidata.org/entity/Q27678722

description

2013 nî lūn-bûn

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2013 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2013 թվականի հունիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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Sequence Determinants of a Specific Inactive Protein Kinase Conformation

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J.CHEMBIOL.2013.05.005

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Chemistry and Biology

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Sequence determinants of a specific inactive protein kinase conformation

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Dustin J Maly

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Ethan A Merritt

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P2860

The protein kinase complement of the human genome

Application of a Theory of Enzyme Specificity to Protein Synthesis

A conserved protonation-dependent switch controls drug binding in the Abl kinase

A simple method for displaying the hydropathic character of a protein

Structural mechanism for STI-571 inhibition of abelson tyrosine kinase

Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site

The structural basis for autoinhibition of FLT3 by the juxtamembrane domain

Synthesis, structural analysis, and SAR studies of triazine derivatives as potent, selective Tie-2 inhibitors

c-Src binds to the cancer drug imatinib with an inactive Abl/c-Kit conformation and a distributed thermodynamic penalty

Biphenyl amide p38 kinase inhibitors 4: DFG-in and DFG-out binding modes

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806-815

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scholarly article

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4014849

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10.1016/J.CHEMBIOL.2013.05.005

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6

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23790491

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clinical chemistry

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3742363

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