Journal:Protein Science:4

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<b>Molecular Tour</b><br>
<b>Molecular Tour</b><br>
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[[Image:2024_Lushchekina_Prot_Sci_x.jpg| thumb |left|150px|For a divalent cation, it is quite hard (takes significant energy) to unbind from structural motifs composed of four acidic residues (4A). However, it is much easier in motifs where three surrounding basic residues form ion pairs with three carboxylates (4A/3B). In contrast to the 4A motif, the 4A/3B motif does not undergo a conformational change upon binding or unbinding the divalent cation. For details, see: Joel Sussman et al., Protein Science, 2024, https://doi.org/10.1002/pro.5206]]''Torpedo californica'' acetylcholinesterase (''Tc''AChE) contains a unique 4D motif composed of four aspartate residues that can bind divalent metal cations (like Ca²⁺, Mg²⁺, Mn²⁺), significantly increasing the enzyme’s thermal stability. Despite the electrostatic repulsion expected between these aspartates, structural analysis shows that the enzyme's conformation remains stable
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[[Image:2024_Lushchekina_Prot_Sci_x.jpg| thumb |left|150px|For a divalent cation, it is quite hard to unbind from structural motifs composed of 4 acidic residues (4A). However, it is much easier in motifs where three surrounding basic residues form ion pairs with three carboxylates (4A/3B), and not undergo a conformational change upon binding or unbinding the divalent cation.]]''Torpedo californica'' acetylcholinesterase (''Tc''AChE) contains a unique 4D motif composed of four aspartate residues that can bind divalent metal cations (like Ca²⁺, Mg²⁺, Mn²⁺), significantly increasing the enzyme’s thermal stability. Despite the electrostatic repulsion expected between these aspartates, structural analysis shows that the enzyme's conformation remains stable
<scene name='10/1063617/009_fig_metal_tcache_lab_png/2'>with</scene> or <scene name='10/1063617/009_fig_apo_tcache_lab_png/2'>without</scene> bound cations as seen in an <scene name='10/1063617/009_fig_metal_apo_tcache_lab/2'>overlay</scene> the two states and an <jmol>
<scene name='10/1063617/009_fig_metal_tcache_lab_png/2'>with</scene> or <scene name='10/1063617/009_fig_apo_tcache_lab_png/2'>without</scene> bound cations as seen in an <scene name='10/1063617/009_fig_metal_apo_tcache_lab/2'>overlay</scene> the two states and an <jmol>
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Revision as of 17:43, 18 November 2024

Acetylcholinesterase highlighting the 4A/3B motif

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Proteopedia Page Contributors and Editors (what is this?)

Joel L. Sussman, Jaime Prilusky

This page complements a publication in scientific journals and is one of the Proteopedia's Interactive 3D Complement pages. For aditional details please see I3DC.
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