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Deciphering Mode of Action of Functionally Important Regions in the Intrinsically Disordered Paxillin (Residues 1-313) Using Its Interaction with FAT (Focal Adhesion Targeting Domain of Focal Adhesion Kinase)

PloS one, 2016-02, Vol.11 (2), p.e0150153-e0150153

2016

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Drug design for protein kinases and phosphatases: flexible-receptor docking, binding affinity and specificity, and drug-binding kinetics

Current pharmaceutical design, 2013, Vol.19 (26), p.4739

2013

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Target-based drug discovery: Applications of fluorescence techniques in high throughput and fragment-based screening

Heliyon, 2024-01, Vol.10 (1), p.e23864-e23864, Article e23864

2024

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Deciphering Mode of Action of Functionally Important Regions in the Intrinsically Disordered Paxillin

PloS one, 2016-02, Vol.11 (2), p.e0150153

2016

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Target identification for small-molecule discovery in the FOXO3a tumor-suppressor pathway using a biodiverse peptide library

Cell chemical biology, 2021-11, Vol.28 (11), p.1602-1615.e9

2021

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Influence of kinetics of drug binding on EGFR signaling: A comparative study of three EGFR signaling pathway models

Proteins, structure, function, and bioinformatics, 2011-08, Vol.79 (8), p.2491-2504

2011

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Automation aided optimization of cloning, expression and purification of enzymes of the bacterial sialic acid catabolic and sialylation pathways enzymes for structural studies

Microbial biotechnology, 2018-03, Vol.11 (2), p.420-428

2018

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Deciphering Mode of Action of Functionally Important Regions in the Intrinsically Disordered Paxillin (Residues 1-313) Using Its Interaction with FAT (Focal Adhesion Targeting Domain of Focal Adhesion Kinase)

Drug design for protein kinases and phosphatases: flexible-receptor docking, binding affinity and specificity, and drug-binding kinetics

Target-based drug discovery: Applications of fluorescence techniques in high throughput and fragment-based screening

Deciphering Mode of Action of Functionally Important Regions in the Intrinsically Disordered Paxillin

Target identification for small-molecule discovery in the FOXO3a tumor-suppressor pathway using a biodiverse peptide library

Influence of kinetics of drug binding on EGFR signaling: A comparative study of three EGFR signaling pathway models

Automation aided optimization of cloning, expression and purification of enzymes of the bacterial sialic acid catabolic and sialylation pathways enzymes for structural studies

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