N each cluster co-evolved (results not shown). WhiJ paralogues in S. coelicolor vary considerably in their conservation in other organisms. One (SCO3421) was present in nearly all complex actinomycetes, and the adjacent gene encoding a likely antisigma factor nearly always contained a TTA codon in Streptomycineae (but in no other groups). Another present in all Streptomycineae (SCO4441) was also w
N each cluster co-evolved (results not shown). WhiJ paralogues in S. coelicolor vary considerably in their conservation in other organisms. One (SCO3421) was present in nearly all complex actinomycetes, and the adjacent gene encoding a likely antisigma factor nearly always contained a TTA codon in Streptomycineae (but in no other groups). Another present in all Streptomycineae (SCO4441) was also w
Stars); S. venezuelae (yellow squares)] and Thermobifida fusca (brown crosses). The tree represents a phylogenetic analysis using PHYLIP (Felsenstein, 1989, 2005).FEMS Microbiol Rev 38 (2014) 345??2013 The Author. FEMS Microbiology Reviews published by John Wiley Sons Ltd on behalf of the Federation of European Microbiological SocietiesG. Chandra K.F. Chater6003, 7615). TTA codons were not ass
Stars); S. venezuelae (yellow squares)] and Thermobifida fusca (brown crosses). The tree represents a phylogenetic analysis using PHYLIP (Felsenstein, 1989, 2005).FEMS Microbiol Rev 38 (2014) 345??2013 The Author. FEMS Microbiology Reviews published by John Wiley Sons Ltd on behalf of the Federation of European Microbiological SocietiesG. Chandra K.F. Chater6003, 7615). TTA codons were not ass
Actinobacterial bacteria. These genes are often clustered withone or both types of whiJ-associated genes. Most mycelial actinomycetes have two or three WhiJ paralogues, but K. setae has five, and all streptomycetes have more than 10, sometimes more than 20. Phylogenetic analysis of WhiJ paralogues from four well-studied streptomycetes is shown in Fig. 7. The branching pattern is consistent with un
Actinobacterial bacteria. These genes are often clustered withone or both types of whiJ-associated genes. Most mycelial actinomycetes have two or three WhiJ paralogues, but K. setae has five, and all streptomycetes have more than 10, sometimes more than 20. Phylogenetic analysis of WhiJ paralogues from four well-studied streptomycetes is shown in Fig. 7. The branching pattern is consistent with un
Factor (AbaA-like) Unknown Unknown SapB biosynthetic enzyme; regulator of SapB biosynthesis Possible phosphotransferase Component of conservon6/13; 7/14 9/11 6/10 8/13 8/12 9/14 8/14 3/11; 5/13 14/14 5/14 12/14 6/14 7/13 5/14 9/14 8/11 12/14 6/14 6/14 7/14 6/13 5/14 5/13 7/14 2/12; 7/12 10/12 9/(? (?(TTA) (? (TTA) (TTA) (??40040 (? 43220 (? ??49090 50850 (TTA) 51100 (TTA) 26520 19600 (? ???16190 3
Factor (AbaA-like) Unknown Unknown SapB biosynthetic enzyme; regulator of SapB biosynthesis Possible phosphotransferase Component of conservon6/13; 7/14 9/11 6/10 8/13 8/12 9/14 8/14 3/11; 5/13 14/14 5/14 12/14 6/14 7/13 5/14 9/14 8/11 12/14 6/14 6/14 7/14 6/13 5/14 5/13 7/14 2/12; 7/12 10/12 9/(? (?(TTA) (? (TTA) (TTA) (??40040 (? 43220 (? ??49090 50850 (TTA) 51100 (TTA) 26520 19600 (? ???16190 3