<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Week 5: Protein Design II :: 2026a-sami-tanveer</title><link>https://pages.htgaa.org/2026a/sami-tanveer/homework/week-05-hw-protein-design-part-ii/index.html</link><description>Part A: SOD1 A4V Therapeutic Peptide Design 1. Project Overview &amp; Pharmacological Target This research targets the A4V mutation (Alanine-to-Valine at residue 4) in human Superoxide Dismutase 1 (SOD1). In Pharmaceutical Sciences, this is a critical target for Familial ALS. The mutation destabilizes the N-terminal “zipper” of the protein, leading to the exposure of hydrophobic residues and subsequent toxic aggregation. Our goal is to design a peptide binder that cap-stabilizes this region.</description><generator>Hugo</generator><language>en</language><atom:link href="https://pages.htgaa.org/2026a/sami-tanveer/homework/week-05-hw-protein-design-part-ii/index.xml" rel="self" type="application/rss+xml"/></channel></rss>