|
|
| Line 12: |
Line 12: |
| == Structural highlights == | | == Structural highlights == |
|
| |
|
| CHS active site residues (Cys-His-Asn) and Phe interact with coenzyme A. The Cys residue is the catalytic nucleophile tethering the starting group and the growing polyketide chain<ref>PMID:10653632</ref>.
| | <scene name='87/873790/Cv/3'>CoA binding site</scene>. The Cys residue (3-sulfinoalanine is shown in this case) is the catalytic nucleophile tethering the starting group and the growing polyketide chain<ref>PMID:10653632</ref>. Water molecules are shown as red spheres. |
| | | |
| </StructureSection> | | </StructureSection> |
Revision as of 12:34, 1 February 2021
|
Function
Chalcone synthase (CHS) is essential for the biosynthesis of flavonoids and anthocyanin pigments in plants. CHS condenses p-coumaroyl-CoA and three malonyl-CoA to produce the polyketide naringenin
[1].
Relevance
The CHS biosynthesis product naringenin has inhibitory activity on a Cyt P450 isoform which can have carcinogenic effect [2] and has significant antioxidant properties.
Structural highlights
CoA binding site. The Cys residue (3-sulfinoalanine is shown in this case) is the catalytic nucleophile tethering the starting group and the growing polyketide chain[3]. Water molecules are shown as red spheres.
- ↑ Yu HN, Wang L, Sun B, Gao S, Cheng AX, Lou HX. Functional characterization of a chalcone synthase from the liverwort Plagiochasma appendiculatum. Plant Cell Rep. 2015 Feb;34(2):233-45. doi: 10.1007/s00299-014-1702-8. Epub 2014 , Nov 18. PMID:25404490 doi:https://dx.doi.org/10.1007/s00299-014-1702-8
- ↑ Kanno S, Tomizawa A, Hiura T, Osanai Y, Shouji A, Ujibe M, Ohtake T, Kimura K, Ishikawa M. Inhibitory effects of naringenin on tumor growth in human cancer cell lines and sarcoma S-180-implanted mice. Biol Pharm Bull. 2005 Mar;28(3):527-30. doi: 10.1248/bpb.28.527. PMID:15744083 doi:https://dx.doi.org/10.1248/bpb.28.527
- ↑ Jez JM, Ferrer JL, Bowman ME, Dixon RA, Noel JP. Dissection of malonyl-coenzyme A decarboxylation from polyketide formation in the reaction mechanism of a plant polyketide synthase. Biochemistry. 2000 Feb 8;39(5):890-902. PMID:10653632
|
Chalcone synthase
Updated on 01-February-2021
{"openlevels":0}
- Chalcone synthase
- 1bi5, 1u0v - alCHS 2 - alfalfa
- 1d6f, 1d6i, 1i86, 1i88, 1i89, 1i8b, 1jwx - alCHS 2 (mutant)
- 6dxb - AtCHS - Arabidopsis thaliana
- 6dxd, 6dxe - AtCHS (mutant)
- 4wum - CHS - freesia
- 6dxa - CHS - pine
- 6dx9 - CHS - horsetail
- 7bus - sbCHS - soybean
- 7dx7 - CHS - moss
- 5uc5 - CHS - apple
- 4yjy - CHS 1 - rice
- 6dx8, 6dxc, 6dxf - CHS - Selaginella moellendorffii
- 6cqb - CHS - kava
- Chalcone synthase complex
- 1cgk - alCHS + naringenin
- 1cgz - alCHS + resveratol
- 1u0w - alCHS 2 (mutant) + resveratol
- 1bq6 - alCHS + CoA
- 1d6h - alCHS (mutant) + CoA
- 1cml - alCHS + malonyl-CoA
- 1chw - alCHS (mutant) + hexanoyl-CoA
- 7bur - sbCHS + naringenin
References
