SNP | p-value | score | G1P1 | G0P0 | G1P0 | G0P1 | Locus | Protein | Description | Essentiality Notes from Mycobrowser |
---|---|---|---|---|---|---|---|---|---|---|
147,873 | 0 | 1 | 4100 | 2250 | 9 | 3 | Â | Â | Intergenic, upstream of elongation factor G FusA2 (Rv0120c) | n/a |
184,727 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv0156 | PntAb | Probable NAD(P) transhydrogenase (subunit alpha) PntAb [second part; integral membrane protein] (pyridine nucleotide transhydrogenase subunit alpha) (nicotinamide nucleotide transhydrogenase subunit alpha) | n/a |
268,277 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv0224c | Â | Possible methyltransferase (methylase) | In vitro essential per multiple studies (Minato 2019; DeJesus 2017; Sassetti 2003; Griffin 2011) |
277,862 | 0 | 1 | 4100 | 2250 | 9 | 3 | Â | Â | Intergenic, downstream of FadE4 (Rv0231) and upstream of probable transcriptional regulatory protein (probably TetR/AcrR-family) (Rv0232) | n/a |
438,069 | 0 | 1 | 1 | 2260 | 0 | 4100 | Rv0359 | Â | Probable conserved integral membrane protein | n/a |
1,234,657 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv1108c | XseA | Probable exodeoxyribonuclease VII (large subunit) XseA (exonuclease VII large subunit) | n/a |
1,390,284 | 0 | -1 | 0 | 2260 | 2 | 4100 | Rv1248c | Â | Multifunctional alpha-ketoglutarate metabolic enzyme | In vitro essential per multiple studies (Minato 2019; Carvalho 2010; Sassetti 2003; Griffin 2011) |
1,478,312 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv1317c | AlkA | Probable bifunctional regulatory protein and DNA repair enzyme AlkA (regulatory protein of adaptative response) (methylphosphotriester-DNA–protein-cysteine S-methyltransferase) | n/a |
1,499,291 | 0 | 1 | 4100 | 2250 | 9 | 4 | Rv1330c | PncB1 | Nicotinic acid phosphoribosyltransferase PncB1 | n/a |
1,586,961 | 0 | 1 | 1 | 2260 | 0 | 4100 | Rv1410c | Â | Aminoglycosides/tetracycline-transport integral membrane protein | Essential in murine macrophages (Rengarajan 2005) and murine spleen (Sassetti and Rubin 2003) |
1,739,294 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv1536 | IleS | Isoleucyl-tRNA synthetase IleS | In vitro essential per multiple studies (Minato 2019; DeJesus 2017; Lamichhane 2003; Griffin 2011) |
1,763,524 | 0 | 1 | 1 | 2260 | 0 | 4100 | Rv1559 | IlvA | Probable threonine dehydratase IlvA | In vitro essential (DeJesus 2017; Griffin 2011), non-essential in rich media (Minato 2019) |
1,830,295 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv1628c | Â | Conserved protein | n/a |
2,314,425 | 0 | -1 | 0 | 2260 | 2 | 4100 | Rv2056c | RpsN2 | 30S ribosomal protein S14 RpsN2 | Disruption provides growth advantage (DeJesus 2017) |
2,475,888 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv2210c | IlvE | Branched-chain amino acid transaminase IlvE | In vitro essential (DeJesus 2017; Sassetti 2003; Griffin 2011), non-essential in rich media (Minato 2019) |
2,528,773 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv2254c | Â | Probable integral membrane protein | n/a |
2,658,676 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv2379c | MbtF | Peptide synthetase MbtF (peptide synthase) | n/a |
2,682,593 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv2388c | HemN | Probable oxygen-independent coproporphyrinogen III oxidase HemN (coproporphyrinogenase) (coprogen oxidase) | Essential in murine spleen (Sassetti and Rubin, 2003) |
2,912,516 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv2585c | Â | Possible conserved lipoprotein | n/a |
2,927,291 | 0 | 1 | 4080 | 2250 | 9 | 21 | Rv2598 | Â | Conserved hypothetical protein | n/a |
3,140,153 | 0 | 1 | 4100 | 2250 | 9 | 4 | Rv2833c | UgpB | Probable Sn-glycerol-3-phosphate-binding lipoprotein UgpB | Disruption provides growth advantage (DeJesus 2017) |
3,143,890 | 0 | -1 | 0 | 2260 | 2 | 4100 | Rv2837c | Â | Conserved protein | n/a |
3,235,485 | 0 | 1 | 1 | 2260 | 0 | 4100 | Rv2922c | Smc | Probable chromosome partition protein Smc | n/a |
3,371,365 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv3011c | GatA | Probable glutamyl-tRNA(GLN) amidotransferase (subunit A) GatA (Glu-ADT subunit A) | In vitro essential per multiple studies (Minato 2019; DeJesus 2017; Sassetti 2003; Griffin 2011) |
3,534,980 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv3166c | Â | Conserved hypothetical protein | n/a |
3,773,023 | 0 | -1 | 0 | 2260 | 2 | 4100 | Rv3361c | Â | Conserved protein | n/a |
3,877,256 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv3456c | RplQ | 50S ribosomal protein L17 RplQ | In vitro essential (Minato 2019; Griffin 2011), or mutant shows growth defect (DeJesus 2017) |
3,904,490 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv3484 | CpsA | Possible conserved protein CpsA | Essential in murine spleen (Sassetti and Rubin, 2003) |
3,922,919 | 0 | -1 | 0 | 2260 | 1 | 4100 | Rv3504 | fadE26 | Probable acyl-CoA dehydrogenase FadE26 | n/a |
4,157,578 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv3712 | Â | Possible ligase | In vitro essential per multiple studies (Minato 2019; DeJesus 2017; Sassetti 2003; Griffin 2011) |
4,171,113 | 0 | 1 | 4100 | 2250 | 9 | 3 | Rv3725 | Â | Possible oxidoreductase | Disruption provides growth advantage (DeJesus 2017) |
4,281,133 | 0 | -1 | 0 | 2260 | 2 | 4100 | Rv3816c | Â | Possible acyltransferase | n/a |