Journal:Protein Science:4
From Proteopedia
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<b>Molecular Tour</b><br> | <b>Molecular Tour</b><br> | ||
- | [[Image:2024_Lushchekina_Prot_Sci_x.jpg| thumb |left|150px|For a divalent cation, it is quite hard | + | [[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> | ||
<jmolButton> | <jmolButton> |
Revision as of 17:43, 18 November 2024
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