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4b1f
From Proteopedia
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==Design of Inhibitors of Helicobacter pylori Glutamate Racemase as Selective Antibacterial Agents: Incorporation of Imidazoles onto a Core Pyrazolopyrimidinedione Scaffold to Improve Bioavailabilty== | ==Design of Inhibitors of Helicobacter pylori Glutamate Racemase as Selective Antibacterial Agents: Incorporation of Imidazoles onto a Core Pyrazolopyrimidinedione Scaffold to Improve Bioavailabilty== | ||
| - | <StructureSection load='4b1f' size='340' side='right' caption='[[4b1f]], [[Resolution|resolution]] 2.05Å' scene=''> | + | <StructureSection load='4b1f' size='340' side='right'caption='[[4b1f]], [[Resolution|resolution]] 2.05Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4b1f]] is a 2 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4b1f]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Helicobacter_pylori Helicobacter pylori]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4B1F OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4B1F FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=DGL:D-GLUTAMIC+ACID'>DGL</scene>, <scene name='pdbligand=KRH:5-METHYL-3-(1-METHYL-1H-IMIDAZOL-5-YL)-7-(2-METHYLPROPYL)-2-(NAPHTHALEN-1-YLMETHYL)-2H-PYRAZOLO[3,4-D]PYRIMIDINE-4,6(5H,7H)-DIONE'>KRH</scene | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.05Å</td></tr> |
| - | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=DGL:D-GLUTAMIC+ACID'>DGL</scene>, <scene name='pdbligand=KRH:5-METHYL-3-(1-METHYL-1H-IMIDAZOL-5-YL)-7-(2-METHYLPROPYL)-2-(NAPHTHALEN-1-YLMETHYL)-2H-PYRAZOLO[3,4-D]PYRIMIDINE-4,6(5H,7H)-DIONE'>KRH</scene></td></tr> | |
| - | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4b1f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4b1f OCA], [https://pdbe.org/4b1f PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4b1f RCSB], [https://www.ebi.ac.uk/pdbsum/4b1f PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4b1f ProSAT]</span></td></tr> | |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
== Function == | == Function == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/MURI_HELPJ MURI_HELPJ] Provides the (R)-glutamate required for cell wall biosynthesis (By similarity). |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 4b1f" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 4b1f" style="background-color:#fffaf0;"></div> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Glutamate racemase 3D structures|Glutamate racemase 3D structures]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Helicobacter pylori]] |
| - | [[Category: | + | [[Category: Large Structures]] |
| - | [[Category: Basarab | + | [[Category: Basarab GS]] |
| - | [[Category: Eyermann | + | [[Category: Eyermann CJ]] |
| - | [[Category: Gowravaram | + | [[Category: Gowravaram M]] |
| - | [[Category: Hill | + | [[Category: Hill P]] |
| - | [[Category: Kack | + | [[Category: Kack H]] |
| - | [[Category: Osimoni | + | [[Category: Osimoni E]] |
| - | + | ||
| - | + | ||
Current revision
Design of Inhibitors of Helicobacter pylori Glutamate Racemase as Selective Antibacterial Agents: Incorporation of Imidazoles onto a Core Pyrazolopyrimidinedione Scaffold to Improve Bioavailabilty
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