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1cml

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<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=1cml FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1cml OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1cml RCSB], [http://www.ebi.ac.uk/pdbsum/1cml PDBsum]</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=1cml FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1cml OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1cml RCSB], [http://www.ebi.ac.uk/pdbsum/1cml PDBsum]</span></td></tr>
</table>
</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/CHS2_MEDSA CHS2_MEDSA]] The primary product of this enzyme is 4,2',4',6'-tetrahydroxychalcone (also termed naringenin-chalcone or chalcone) which can under specific conditions spontaneously isomerize into naringenin.<ref>PMID:10653632</ref> <ref>PMID:11732902</ref> <ref>PMID:11959984</ref> <ref>PMID:15380179</ref>
== Evolutionary Conservation ==
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
[[Image:Consurf_key_small.gif|200px|right]]

Revision as of 14:12, 25 December 2014

CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH MALONYL-COA

1cml, resolution 1.69Å

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