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==Amylin==
==Amylin==
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Amylin is extremely conserved among species, in order to maintain proper structure and function. Some of the main <scene name='10/1038871/Conserved_residues/4'>conserved residues</scene> are Lysine 1, Cysteine 2, Alanine 5, Threonine 6, and Cysteine 7. All of the conserved residues exhibit extensive hydrogen bonding networks between either other residues or surrounding water molecules. There is also a [https://en.wikipedia.org/wiki/Disulfide disulfide bond] between <scene name='10/1038871/Disulfide/4'>C2 and C7</scene> that is conserved across almost every species.<ref name="Bower">PMID:27061187</ref>
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Amylin is extremely conserved among species, in order to maintain proper structure and function. Some of the main <scene name='10/1038871/Conserved_residues/5'>conserved residues</scene> are Lysine 1, Cysteine 2, Alanine 5, Threonine 6, and Cysteine 7. All of the conserved residues exhibit extensive hydrogen bonding networks between either other residues or surrounding water molecules. There is also a [https://en.wikipedia.org/wiki/Disulfide disulfide bond] between <scene name='10/1038871/Disulfide/4'>C2 and C7</scene> that is conserved across almost every species.<ref name="Bower">PMID:27061187</ref>

Revision as of 19:39, 16 April 2024

amylin images

Caption for this structure

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References

  1. 1.0 1.1 Bower RL, Hay DL. Amylin structure-function relationships and receptor pharmacology: implications for amylin mimetic drug development. Br J Pharmacol. 2016 Jun;173(12):1883-98. PMID:27061187 doi:10.1111/bph.13496
  2. Cao J, Belousoff MJ, Liang YL, Johnson RM, Josephs TM, Fletcher MM, Christopoulos A, Hay DL, Danev R, Wootten D, Sexton PM. A structural basis for amylin receptor phenotype. Science. 2022 Mar 25;375(6587):eabm9609. PMID:35324283 doi:10.1126/science.abm9609

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Emily Berkman

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