2009
DOI: 10.1107/s1744309109009555
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Cloning, expression, crystallization and preliminary X-ray crystallographic analysis of β-ketoacyl-ACP synthase III (FabH) fromXanthomonas oryzaepv.oryzae

Abstract: The bacterial beta-ketoacyl-ACP synthase III (KASIII) encoded by the gene fabH (Xoo4209) from Xanthomonas oryzae pv. oryzae, a plant pathogen, is an important enzyme in the elongation steps of fatty-acid biosynthesis. It is expected to be one of the enzymes responsible for bacterial blight (BB), a serious disease that results in huge production losses of rice. As it represents an important target for the development of new antibacterial drugs against BB, determination of the crystal structure of the KAS III en… Show more

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Cited by 3 publications
(3 citation statements)
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References 18 publications
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“…Little is known of the biosynthetic mechanisms of these fatty acids except that Xanthomonas oryzae pv. oryzae FabD, FabB, FabH and FabV have been expressed and crystallized 26 27 28 29 .…”
mentioning
confidence: 99%
“…Little is known of the biosynthetic mechanisms of these fatty acids except that Xanthomonas oryzae pv. oryzae FabD, FabB, FabH and FabV have been expressed and crystallized 26 27 28 29 .…”
mentioning
confidence: 99%
“…Although the fatty acid profiles of Xanthomonas have been investigated for taxonomic purposes 22 23 24 , and several fatty acid synthetic enzymes, including FabD, FabB, FabH, and FabV from Xanthomonas oryzae pv. oryzae 25 26 27 28 , have been expressed and crystallized, little is known about the fatty acid biosynthetic pathway in Xanthomonas .…”
mentioning
confidence: 99%
“…Docking Study. Molecular docking of isolated compounds into the 3D X-ray structure of XooFabH (PDB: 3FK5) 31 was conducted using Discovery Studio 3.5 using a graphical user interface DS-CDocker protocol. The 3D structures of compounds were drawn using ChemBioDraw Ultra 14.0 (Cambridge Soft corporation) with the mol format and were imported into Discovery Studio 3.5.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%