Protein-peptide interactions between P5 and Jun N-terminal kinase1.

<p>(a) Receptor protein is represented in green with cyan interacting residues. The peptide P5 is shown in magenta with its interacting residues. (b) Residual interactions between P5 and protein complex. Hydrogen bonds are represented in green color.</p>

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Bibliographic Details
Main Author:	Anas Bilal (11785200) (author)
Other Authors:	Ghulam Mustafa (458105) (author)
Published:	2025
Subjects:	Biophysics Biochemistry Genetics Molecular Biology Pharmacology Biotechnology Cancer Biological Sciences not elsewhere classified Chemical Sciences not elsewhere classified seven hydrogen bonds selected diabetic proteins regulate glucose absorption potential therapeutic candidates harmful side effects explored using peptide active packaging systems synthetic agents used hydrogen bond interactions computational study support xlink "> diabetes particular protein fragments develop hypoglycemic peptides protein docking particular peptides hypoglycemic peptides current study binding interactions antidiabetic agents target receptors taken orally simulation time silico </ plant sources physiological processes peptides p5 pancreatic alpha metabolic disease leading causes jun n human health haddock energy functional materials firmly bound extremely difficult different number diabetes mellitus data showing bioactive peptides binding patterns binding pattern binding energy beneficial impact affect people 4 kcal 3 kcal 100 ns 1 kcal &# 8722
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Protein-peptide interactions between P5 and Jun N-terminal kinase1.

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