6bur
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structures of cyanuric acid hydrolase from Moorella thermoacetica complexed with barbituric acid== | |
| - | + | <StructureSection load='6bur' size='340' side='right'caption='[[6bur]], [[Resolution|resolution]] 2.18Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6bur]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6BUR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6BUR FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BR8:BARBITURIC+ACID'>BR8</scene>, <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=MLI:MALONATE+ION'>MLI</scene></td></tr> | |
| - | [[Category: | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Cyanuric_acid_amidohydrolase Cyanuric acid amidohydrolase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.15 3.5.2.15] </span></td></tr> |
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6bur FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bur OCA], [http://pdbe.org/6bur PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6bur RCSB], [http://www.ebi.ac.uk/pdbsum/6bur PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6bur ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/CAH_MOOTA CAH_MOOTA]] Responsible for the hydrolysis of cyanuric acid, an intermediate formed during catabolism of s-triazine based compounds in herbicides such as atrazine and polymers such as melamine. Catalyzes the hydrolytic opening of the s-triazine ring of cyanuric acid (2,4,6-trihydroxy-s-triazine) to yield carbon dioxide and carboxybiuret, which spontaneously decarboxylates to biuret.[HAMAP-Rule:MF_01989]<ref>PMID:19767460</ref> <ref>PMID:28235873</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Cyanuric acid amidohydrolase]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Aihara, H]] | ||
| + | [[Category: Shi, K]] | ||
| + | [[Category: Cyanuric acid hydrolase]] | ||
| + | [[Category: Hydrolase]] | ||
Revision as of 05:28, 12 June 2019
Crystal structures of cyanuric acid hydrolase from Moorella thermoacetica complexed with barbituric acid
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