Structure-guided design of a potent peptide inhibitor targeting the interaction between CRK and ABL kinase-Reference-Cited by-同舟云学术

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Structure-guided design of a potent peptide inhibitor targeting the interaction between CRK and ABL kinase

Published:2018 Issue:3 Volume:9 Page:519-524
ISSN:2040-2503
Container-title:MedChemComm
language:en
Short-container-title:Med. Chem. Commun.

Author:

Shen Qingliang¹²³⁴,Bhatt Veer S.¹²³⁴,Krieger Inna¹²³⁴,Sacchettini James C.¹²³⁴,Cho Jae-Hyun¹²³⁴^ORCID

Affiliation:

1. Department of Biochemistry and Biophysics

2. Texas A&M University

3. College Station

4. USA

Abstract

CT-10 regulator of kinase (CRK) proteins play important roles in human cancer metastasis and invasion.

Funder

Texas A&M University

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/MD/C7MD00619E

Reference36 articles.

1. Small-Molecule Inhibitors of Protein-Protein Interactions: Progressing toward the Reality

2. Inhibiting fungal multidrug resistance by disrupting an activator–Mediator interaction

3. SH3 domain ligand binding: What's the consensus and where's the specificity?

4. SH3 Domains: Molecular ‘Velcro’

5. How SH3 domains recognize proline

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Crk1/2 and CrkL play critical roles in maintaining podocyte morphology and function;Experimental Cell Research;2020-09

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