Strain Fitness in Rhodospirillum rubrum S1H around Rru_A1773

Experiment: carbon source anaerobic Succinic Acid 31.25 mM

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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 ntRru_A1771 and Rru_A1772 are separated by 45 nucleotidesRru_A1772 and Rru_A1773 are separated by 76 nucleotidesRru_A1773 and Rru_A1774 are separated by 273 nucleotidesRru_A1774 and Rru_A1775 overlap by 4 nucleotides Rru_A1771: Rru_A1771 - Sec-independent periplasmic protein translocase (NCBI), at 2,063,647 to 2,064,618 _A1771 Rru_A1772: Rru_A1772 - Twin-arginine translocation protein TatB (NCBI), at 2,064,664 to 2,065,116 _A1772 Rru_A1773: Rru_A1773 - Twin-arginine translocation protein TatA/E (NCBI), at 2,065,193 to 2,065,483 _A1773 Rru_A1774: Rru_A1774 - Predicted transcriptional regulator (NCBI), at 2,065,757 to 2,066,476 _A1774 Rru_A1775: Rru_A1775 - chromosome segregation and condensation protein ScpA (NCBI), at 2,066,473 to 2,067,285 _A1775 Position (kb) 2065 2066Strain fitness (log2 ratio) -2 -1 0 1at 2065.563 kb on - strandat 2065.758 kb on + strandat 2065.865 kb on - strand, within Rru_A1774

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Per-strain Table

Position Strand Gene LocusTag Fraction carbon source anaerobic Succinic Acid 31.25 mM
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2,065,563 - -2.1
2,065,758 + -0.5
2,065,865 - Rru_A1774 0.15 +0.2

Or see this region's nucleotide sequence