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Protein
Homologs
Fitness for 5 genes in
Escherichia coli ECRC101
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Top 26 experiments (either direction), sorted by average fitness
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500 nt
MCAODC_25795 and MCAODC_25800 are separated by 183 nucleotides
MCAODC_25800 and MCAODC_25805 are separated by 474 nucleotides
MCAODC_25805 and MCAODC_25810 are separated by 211 nucleotides
MCAODC_25810 and ninG overlap by 4 nucleotides
MCAODC_25795: MCAODC_25795 - Membrane protein, at 1,879,763 to 1,880,506
_25795
MCAODC_25800: MCAODC_25800 - antitermination protein, at 1,880,690 to 1,881,379
_25800
MCAODC_25805: MCAODC_25805 - DUF2219 domain-containing protein, at 1,881,854 to 1,882,813
_25805
MCAODC_25810: MCAODC_25810 - Serine/threonine-protein phosphatase, at 1,883,025 to 1,883,690
_25810
MCAODC_25815: ninG - Protein ninG, at 1,883,687 to 1,884,307
ninG
Group
Condition
MCAODC
_25795
MCAODC
_25800
MCAODC
_25805
MCAODC
_25810
MCAODC
_25815
ninG
phage
Bas09
N.D.
-0.7
-0.3
N.D.
N.D.
phage
EV240
N.D.
-0.2
-0.4
N.D.
N.D.
phage
Bas14
N.D.
-0.3
-0.2
N.D.
N.D.
carbon source
D-Glucose
N.D.
-0.6
+0.1
N.D.
N.D.
phage
Bas14
N.D.
-0.7
+0.2
N.D.
N.D.
no phage control
Control_ECRC101_WM
N.D.
-0.1
-0.4
N.D.
N.D.
carbon source
Sodium-DL-Lactate
N.D.
-0.4
+0.0
N.D.
N.D.
phage
WM_TP9
N.D.
+0.0
-0.4
N.D.
N.D.
no phage control
Control_ECRC101_WM
N.D.
-0.1
-0.2
N.D.
N.D.
phage
Bas09
N.D.
-0.4
+0.1
N.D.
N.D.
phage
WM_Bas41
N.D.
-0.0
-0.2
N.D.
N.D.
carbon source
Casamino-acids
N.D.
-0.4
+0.1
N.D.
N.D.
phage
WM_Bas09
N.D.
+0.1
-0.2
N.D.
N.D.
phage
WM_Bas14
N.D.
-0.1
+0.0
N.D.
N.D.
phage
EV240
N.D.
-0.4
+0.3
N.D.
N.D.
phage
WM_RB68
N.D.
+0.1
-0.2
N.D.
N.D.
phage
WM_EV240
N.D.
+0.2
-0.2
N.D.
N.D.
carbon source
L-Arabinose
N.D.
+0.1
-0.0
N.D.
N.D.
phage
WM_TP9
N.D.
+0.2
-0.1
N.D.
N.D.
phage
WM_Bas09
N.D.
+0.1
-0.0
N.D.
N.D.
carbon source
D-Glucose
N.D.
-0.4
+0.5
N.D.
N.D.
carbon source
Casamino-acids
N.D.
+0.2
-0.0
N.D.
N.D.
phage
TP9
N.D.
-0.0
+0.2
N.D.
N.D.
carbon source
Sodium-DL-Lactate
N.D.
-0.2
+0.5
N.D.
N.D.
carbon source
L-Arabinose
N.D.
+0.2
+0.1
N.D.
N.D.
phage
WM_EV240
N.D.
+0.1
+0.2
N.D.
N.D.
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