1chw: Difference between revisions

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New page: left|200px<br /><applet load="1chw" size="450" color="white" frame="true" align="right" spinBox="true" caption="1chw, resolution 1.9Å" /> '''CHALCONE SYNTHASE FRO...
 
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[[Image:1chw.jpg|left|200px]]<br /><applet load="1chw" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1chw.jpg|left|200px]]<br /><applet load="1chw" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1chw, resolution 1.9&Aring;" />
caption="1chw, resolution 1.9&Aring;" />
'''CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH HEXANOYL-COA'''<br />
'''CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH HEXANOYL-COA'''<br />


==Overview==
==Overview==
Chalcone synthase (CHS) is pivotal for the biosynthesis of flavonoid, antimicrobial phytoalexins and anthocyanin pigments in plants. It produces, chalcone by condensing one p-coumaroyl- and three malonyl-coenzyme A, thioesters into a polyketide reaction intermediate that cyclizes. The, crystal structures of CHS alone and complexed with substrate and product, analogs reveal the active site architecture that defines the sequence and, chemistry of multiple decarboxylation and condensation reactions and, provides a molecular understanding of the cyclization reaction leading to, chalcone synthesis. The structure of CHS complexed with resveratrol also, suggests how stilbene synthase, a related enzyme, uses the same substrates, and an alternate cyclization pathway to form resveratrol. By using the, three-dimensional structure and the large database of CHS-like sequences, we can identify proteins likely to possess novel substrate and product, specificity. The structure elucidates the chemical basis of plant, polyketide biosynthesis and provides a framework for engineering CHS-like, enzymes to produce new products.
Chalcone synthase (CHS) is pivotal for the biosynthesis of flavonoid antimicrobial phytoalexins and anthocyanin pigments in plants. It produces chalcone by condensing one p-coumaroyl- and three malonyl-coenzyme A thioesters into a polyketide reaction intermediate that cyclizes. The crystal structures of CHS alone and complexed with substrate and product analogs reveal the active site architecture that defines the sequence and chemistry of multiple decarboxylation and condensation reactions and provides a molecular understanding of the cyclization reaction leading to chalcone synthesis. The structure of CHS complexed with resveratrol also suggests how stilbene synthase, a related enzyme, uses the same substrates and an alternate cyclization pathway to form resveratrol. By using the three-dimensional structure and the large database of CHS-like sequences, we can identify proteins likely to possess novel substrate and product specificity. The structure elucidates the chemical basis of plant polyketide biosynthesis and provides a framework for engineering CHS-like enzymes to produce new products.


==About this Structure==
==About this Structure==
1CHW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Medicago_sativa Medicago sativa] with HXC as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Naringenin-chalcone_synthase Naringenin-chalcone synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.74 2.3.1.74] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CHW OCA].  
1CHW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Medicago_sativa Medicago sativa] with <scene name='pdbligand=HXC:'>HXC</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Naringenin-chalcone_synthase Naringenin-chalcone synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.74 2.3.1.74] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CHW OCA].  


==Reference==
==Reference==
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[[Category: Naringenin-chalcone synthase]]
[[Category: Naringenin-chalcone synthase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Bowman, M.E.]]
[[Category: Bowman, M E.]]
[[Category: Dixon, R.]]
[[Category: Dixon, R.]]
[[Category: Ferrer, J.L.]]
[[Category: Ferrer, J L.]]
[[Category: Jez, J.]]
[[Category: Jez, J.]]
[[Category: Noel, J.P.]]
[[Category: Noel, J P.]]
[[Category: HXC]]
[[Category: HXC]]
[[Category: chalcone biosynthesis]]
[[Category: chalcone biosynthesis]]
[[Category: polyketide synthase]]
[[Category: polyketide synthase]]


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