Journal:Protein Science:4
From Proteopedia
(Difference between revisions)

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<StructureSection load='' size='340' side='right' scene='10/1063617/009_figu_5b_png/3' caption='Acetylcholinesterase highlighting the 4A/3B motif'> | <StructureSection load='' size='340' side='right' scene='10/1063617/009_figu_5b_png/3' caption='Acetylcholinesterase highlighting the 4A/3B motif'> | ||
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===Why is binding of a divalent metal cation to a structural motif containing four carboxylate residues not accompanied by a conformational change?=== | ===Why is binding of a divalent metal cation to a structural motif containing four carboxylate residues not accompanied by a conformational change?=== | ||
- | <big>Lushchekina, Weiner, Ashani, Emrizal, Firdaus-Raih, Silman & Sussman</big><ref>PMID: 39548604</ref> | + | [[Image:2024_Lushchekina_Prot_Sci_x.jpg| thumb |left150px]]<br /><big>Lushchekina, Weiner, Ashani, Emrizal, Firdaus-Raih, Silman & Sussman</big><ref>PMID: 39548604</ref> |
<hr/> | <hr/> | ||
<b>Molecular Tour</b><br> | <b>Molecular Tour</b><br> |
Revision as of 17:36, 18 November 2024
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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.