7bm4
From Proteopedia
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<StructureSection load='7bm4' size='340' side='right'caption='[[7bm4]], [[Resolution|resolution]] 1.60Å' scene=''> | <StructureSection load='7bm4' size='340' side='right'caption='[[7bm4]], [[Resolution|resolution]] 1.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'> | + | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7BM4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7BM4 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=U3N:1-(4-fluorophenyl)-3-(4-sulfamoylphenyl)selenourea'>U3N</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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]] 1.6Å</td></tr> |
| - | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=U3N:1-(4-fluorophenyl)-3-(4-sulfamoylphenyl)selenourea'>U3N</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | |
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7bm4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bm4 OCA], [https://pdbe.org/7bm4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bm4 RCSB], [https://www.ebi.ac.uk/pdbsum/7bm4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bm4 ProSAT]</span></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=7bm4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bm4 OCA], [https://pdbe.org/7bm4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bm4 RCSB], [https://www.ebi.ac.uk/pdbsum/7bm4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bm4 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| - | == Function == | ||
| - | [[https://www.uniprot.org/uniprot/A0A3Q0KSG2_SCHMA A0A3Q0KSG2_SCHMA]] Reversible hydration of carbon dioxide.[RuleBase:RU367011] | ||
| - | <div style="background-color:#fffaf0;"> | ||
| - | == Publication Abstract from PubMed == | ||
| - | Tegumental carbonic anhydrase from the worm Schistosoma mansoni (SmCA) is considered a new anti-parasitic target because suppressing its expression interferes with schistosome metabolism and virulence. Here, we present the inhibition profiles of selenoureido compounds on recombinant SmCA and resolution of the first X-ray crystal structures of SmCA in adduct with a selection of such inhibitors. The key molecular features of such compounds in adduct with SmCA were obtained and compared to the human isoform hCA II, in order to understand the main structural factors responsible for enzymatic affinity and selectivity. Compounds that more specifically inhibited the schistosome versus human enzymes were identified. The results expand current knowledge in the field and pave the way for the development of more potent antiparasitic agents in the near future. | ||
| - | + | ==See Also== | |
| - | + | *[[Carbonic anhydrase 3D structures|Carbonic anhydrase 3D structures]] | |
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: Carbonate dehydratase]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Angeli | + | [[Category: Angeli A]] |
| - | [[Category: Ferraroni | + | [[Category: Ferraroni M]] |
| - | [[Category: Supuran | + | [[Category: Supuran CT]] |
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Current revision
Crystal structure of alpha Carbonic anhydrase from Schistosoma mansoni bound to 1-(4-fluorophenyl)-3-(4-sulphamoylphenyl)selenourea
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