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Peptide: difference between revisions

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Revision 8 — 12:12, 16 Aug 2024
CDMO_Caradoc (talk)
expand §Peptides in research supply
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Revision 9 — 19:05, 30 Aug 2024
CRP_Cormac (talk)
clarify that the cake appearance is an indicator, not a specification
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19Side chains determine chemistry. Charged residues set the isoelectric point and therefore the pH of minimum solubility; hydrophobic residues drive [[Peptide aggregation|aggregation]]; asparagine, glutamine and methionine introduce the specific chemical liabilities discussed at [[Deamidation]] and [[Methionine oxidation]].19Side chains determine chemistry. Charged residues set the isoelectric point and therefore the pH of minimum solubility; hydrophobic residues drive [[Peptide aggregation|aggregation]]; asparagine, glutamine and methionine introduce the specific chemical liabilities discussed at [[Deamidation]] and [[Methionine oxidation]].
2020
+21== Nomenclature and notation ==
+22| Notation | Meaning |
+23|---|---|
+24| Three-letter code | Ala, Gly, Lys — used for readability |
+25| One-letter code | A, G, K — used for long sequences |
+26| Lower-case letter | D-amino acid, in some conventions |
+27| Aib | α-aminoisobutyric acid, a common non-proteinogenic residue |
+28| Numbering | From the N-terminus of the mature peptide unless stated |
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+30Numbering is a frequent source of confusion in the incretin literature, because GLP-1 is numbered from the N-terminus of proglucagon-derived GLP-1(1–37) while its active form begins at residue 7. The same substitution is therefore described as being at position 2 or position 8 depending on convention, which is why [[Semaglutide|semaglutide]] is described both as having Aib at position 8 and as having a substitution at the second residue of the active peptide.{{r|iupac}}
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21== References ==32== References ==
22{{reflist}}33{{reflist}}