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4b1c
From Proteopedia
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==New Aminoimidazoles as BACE-1 Inhibitors: From Rational Design to Ab- lowering in Brain== | ==New Aminoimidazoles as BACE-1 Inhibitors: From Rational Design to Ab- lowering in Brain== | ||
| - | <StructureSection load='4b1c' size='340' side='right' caption='[[4b1c]], [[Resolution|resolution]] 1.95Å' scene=''> | + | <StructureSection load='4b1c' size='340' side='right'caption='[[4b1c]], [[Resolution|resolution]] 1.95Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4b1c]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4b1c]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4B1C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4B1C FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=1B1:(2R)-2-CYCLOPROPYL-5-METHYL-2-[3-(5-PROP-1-YN-1-YLPYRIDIN-3-YL)PHENYL]-2H-IMIDAZOL-4-AMINE'>1B1</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=1B1:(2R)-2-CYCLOPROPYL-5-METHYL-2-[3-(5-PROP-1-YN-1-YLPYRIDIN-3-YL)PHENYL]-2H-IMIDAZOL-4-AMINE'>1B1</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene></td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1fkn|1fkn]], [[1m4h|1m4h]], [[1py1|1py1]], [[1sgz|1sgz]], [[1tqf|1tqf]], [[1ujj|1ujj]], [[1ujk|1ujk]], [[1w50|1w50]], [[1w51|1w51]], [[1xn2|1xn2]], [[1xn3|1xn3]], [[1xs7|1xs7]], [[1ym2|1ym2]], [[1ym4|1ym4]], [[2b8l|2b8l]], [[2b8v|2b8v]], [[2fdp|2fdp]], [[2va5|2va5]], [[2va6|2va6]], [[2va7|2va7]], [[2vie|2vie]], [[2vij|2vij]], [[2viy|2viy]], [[2viz|2viz]], [[2vj6|2vj6]], [[2vj7|2vj7]], [[2vj9|2vj9]], [[2vkm|2vkm]], [[2vnm|2vnm]], [[2vnn|2vnn]], [[2wez|2wez]], [[2wf0|2wf0]], [[2wf1|2wf1]], [[2wf2|2wf2]], [[2wf3|2wf3]], [[2wf4|2wf4]], [[2wjo|2wjo]], [[2xfi|2xfi]], [[2xfj|2xfj]], [[2xfk|2xfk]], [[4acu|4acu]], [[4acx|4acx]], [[4azy|4azy]], [[4b00|4b00]], [[4b05|4b05]], [[4b0q|4b0q]], [[4b1d|4b1d]], [[4b1e|4b1e]]</td></tr> | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1fkn|1fkn]], [[1m4h|1m4h]], [[1py1|1py1]], [[1sgz|1sgz]], [[1tqf|1tqf]], [[1ujj|1ujj]], [[1ujk|1ujk]], [[1w50|1w50]], [[1w51|1w51]], [[1xn2|1xn2]], [[1xn3|1xn3]], [[1xs7|1xs7]], [[1ym2|1ym2]], [[1ym4|1ym4]], [[2b8l|2b8l]], [[2b8v|2b8v]], [[2fdp|2fdp]], [[2va5|2va5]], [[2va6|2va6]], [[2va7|2va7]], [[2vie|2vie]], [[2vij|2vij]], [[2viy|2viy]], [[2viz|2viz]], [[2vj6|2vj6]], [[2vj7|2vj7]], [[2vj9|2vj9]], [[2vkm|2vkm]], [[2vnm|2vnm]], [[2vnn|2vnn]], [[2wez|2wez]], [[2wf0|2wf0]], [[2wf1|2wf1]], [[2wf2|2wf2]], [[2wf3|2wf3]], [[2wf4|2wf4]], [[2wjo|2wjo]], [[2xfi|2xfi]], [[2xfj|2xfj]], [[2xfk|2xfk]], [[4acu|4acu]], [[4acx|4acx]], [[4azy|4azy]], [[4b00|4b00]], [[4b05|4b05]], [[4b0q|4b0q]], [[4b1d|4b1d]], [[4b1e|4b1e]]</div></td></tr> |
| - | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Memapsin_2 Memapsin 2], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.46 3.4.23.46] </span></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4b1c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4b1c OCA], [https://pdbe.org/4b1c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4b1c RCSB], [https://www.ebi.ac.uk/pdbsum/4b1c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4b1c ProSAT]</span></td></tr> |
</table> | </table> | ||
== Function == | == Function == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/BACE1_HUMAN BACE1_HUMAN]] Responsible for the proteolytic processing of the amyloid precursor protein (APP). Cleaves at the N-terminus of the A-beta peptide sequence, between residues 671 and 672 of APP, leads to the generation and extracellular release of beta-cleaved soluble APP, and a corresponding cell-associated C-terminal fragment which is later released by gamma-secretase.<ref>PMID:10677483</ref> <ref>PMID:20354142</ref> |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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==See Also== | ==See Also== | ||
| - | *[[Beta secretase|Beta secretase]] | + | *[[Beta secretase 3D structures|Beta secretase 3D structures]] |
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Human]] | [[Category: Human]] | ||
| + | [[Category: Large Structures]] | ||
[[Category: Memapsin 2]] | [[Category: Memapsin 2]] | ||
| - | [[Category: Berg, S]] | + | [[Category: Berg, S von]] |
[[Category: Blid, J]] | [[Category: Blid, J]] | ||
[[Category: Eketjall, S]] | [[Category: Eketjall, S]] | ||
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[[Category: Johansson, P]] | [[Category: Johansson, P]] | ||
[[Category: Karlstrom, S]] | [[Category: Karlstrom, S]] | ||
| - | [[Category: Kieseritzky, F]] | + | [[Category: Kieseritzky, F von]] |
[[Category: Kihlstrom, J]] | [[Category: Kihlstrom, J]] | ||
[[Category: Kolmodin, K]] | [[Category: Kolmodin, K]] | ||
Current revision
New Aminoimidazoles as BACE-1 Inhibitors: From Rational Design to Ab- lowering in Brain
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Categories: Human | Large Structures | Memapsin 2 | Berg, S von | Blid, J | Eketjall, S | Falting, J | Ginman, T | Gravenfors, Y | Janson, J | Jeppsson, F | Johansson, P | Karlstrom, S | Kieseritzky, F von | Kihlstrom, J | Kolmodin, K | Lindstrom, J | Olsson, L | Rahm, F | Slivo, C | Stromberg, K | Swahn, B | Viklund, J | Hydrolase | Inhibitor | Lead generation | Structure-based drug design
