Strain Fitness in Escherichia coli ECRC102 around NIAGMN_24260

Experiment: D-Glucose

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Only strains with sufficient reads to estimate fitness are shown, but the strain fitness values are still rather noisy and may be biased towards zero. Strains near the edge of a gene are not shown as being associated with that gene (they are in grey). Strains in the central 10-90% of a gene are color coded by the insertion's strand. Usually, "+" means that the selectable marker is encoded on the forward strand, i.e., transcribed rightward.

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500 ntNIAGMN_24250 and fabG are separated by 12 nucleotidesfabG and acpP are separated by 210 nucleotidesacpP and fabF are separated by 87 nucleotides NIAGMN_24250: NIAGMN_24250 - ACP S-malonyltransferase, at 4,742,565 to 4,743,494 _24250 NIAGMN_24255: fabG - 3-oxoacyl-ACP reductase FabG, at 4,743,507 to 4,744,241 fabG NIAGMN_24260: acpP - acyl carrier protein, at 4,744,452 to 4,744,688 acpP NIAGMN_24265: fabF - beta-ketoacyl-ACP synthase II, at 4,744,776 to 4,746,017 fabF Position (kb) 4744 4745Strain fitness (log2 ratio) -1 0 1at 4743.492 kb on + strandat 4744.296 kb on + strandat 4744.296 kb on + strandat 4744.743 kb on + strandat 4744.792 kb on + strand

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Per-strain Table

Position Strand Gene LocusTag Fraction D-Glucose
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4,743,492 + +0.6
4,744,296 + +0.5
4,744,296 + -0.4
4,744,743 + +1.6
4,744,792 + -0.5

Or see this region's nucleotide sequence