Factor type | Unique (DeoR family) |
---|---|
SWISS-PROT | ND |
SubtiList | ND |
Consensus seq. | WWRRACAR-Y |
Comment | A bi-functional transcription factor which regulates temporal expression of many genes in the mother cell as well as GerE |
Link to | Phylogenetic profile, Weight matrix & Motif alignment |
Operon | Regulated Gene | Sigma | Regulation | Absolute position | Location | Binding seq.(cis-element) | Experimental evidence |
---|---|---|---|---|---|---|---|
asnO | asnO | SigE | Positive | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
bofA | bofA | SigE | Negative | 29727..29756 | -17:+13 | TCTCATAAGCTTGTACTAGAACAAGCGAAG |
Ireton K & Grossman AD (1992): RG DB Halberg R, et al. (1994): FT RO Eichenberger P, et al. (2004): GS AR |
bofA | bofA | SigE | Negative | 29797..29817 | +54:+74 | TTATTTTAGGACTGGTTATTC |
Ireton K & Grossman AD (1992): RG DB Halberg R, et al. (1994): FT RO Eichenberger P, et al. (2004): GS AR |
cotA | cotA | SigK | Negative | ND | ND | ND |
Halberg R, et al. (1995): RO |
cotC | cotC | SigK | Negative | 1905237..1905307 | -86:-16 | TCTTTTTCTATCATTTGGACAGCCCTTTTTTCCTTCTATGATTTTAACTGTCCAAGCCGCAAAATCTACTC |
Ichikawa H, et al. (2000): GS FT |
cotD | cotD | SigK | Negative | 2333101..2333121 | -79:-59 | AAAGACAGCTTAATTGCACAC |
Halberg R, et al. (1994): FT RO |
cotD | cotD | SigK | Negative | 2333063..2333082 | -40:-21 | CATCAGAACATGTACCCCTT |
Halberg R, et al. (1994): FT RO |
cotD | cotD | SigK | Negative | 2332964..2332989 | +54:+79 | TGATGGCGCCAATTGTCCATCCTACT |
Halberg R, et al. (1994): FT RO |
cotF | cotF | SigK | Positive | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
cotJABC-yesJK | cotJA | SigE | Positive | 755829..755858 | -48:-19 | AAGTCGTGTTTTAGTCATAATCATGCCTCC |
Henriques AO, et al. (1995): DB RG |
cotT | cotT | SigK | Positive | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
cotVWX | cotX | SigK | Negative | 1251201..1251230 | -35:-7 | AGTCAAAATAAGAGGCTCGCTCATTTAATA |
Ichikawa H, et al. (2000): GS FT |
gerE | gerE | SigK | Positive | ND | ND | ND |
Halberg R, et al. (1995): RO |
gerM | gerM | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
spoIID | spoIID | SigE | Negative | 3777784..3777844 | -60:+1 | ATAAAGTTTCTGTCCAAAACGAGAGTCATATTAGCTTGTCCCTGCCCATAGACTAGACTAG |
Eichenberger P, et al. (2004): FT GS AR |
yqhV-spoIIIAABCDEFGH | spoIIIAA | SigE | Negative | 2537640..2537697 | -55:+3 | CATAAATAAAGAGAGGCTTGTCATAAAGTCTGCCTCACATCATACATTTTAAAGAAGC |
Eichenberger P, et al. (2004): FT AR |
yqhV-spoIIIAABCDEFGH | spoIIIAG | SigE | Negative | 2534009..2534062 | -40:+14 | AAATAGAAATACAAGCTTCCCAGCGCGCATATATTCTAGAAGAAATGGCTGTCC |
Guillot C, et al. (2007): DB,RG,PE,HM |
spoIVA | spoIVA | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
spoIVCA | spoIVCA | SigE | Positive | 2654997..2655030 | -47:-12 | TTAAAATCTCCTCATTTGGACAAACAGCTGTTAC |
Halberg R, et al. (1994): FT RO Eichenberger P, et al. (2004): GS AR |
spoIVCA | spoIVCA | SigE | Positive | 2654831..2654848 | +137:+154 | CGACCGAGGAACAAGCGA |
Halberg R, et al. (1994): FT RO Eichenberger P, et al. (2004): GS AR |
spoIVCB-spoIIIC | spoIVCB | SigE | Positive | 2652918..2652938 | -36:-16 | TACAGACACAGACAGCCTCCC |
Halberg R, et al. (1994): FT RO |
spoIVCB-spoIIIC | spoIVCB | SigE | Positive | 2653031..2653053 | +78:+100 | TAAAGAGCTTGTCTTTTTAGTAT |
Halberg R, et al. (1994): FT RO |
spoIVCB-spoIIIC | spoIVCB | SigE | Positive | 2653062..2653086 | +109:+133 | AAAAACAATGCCTTTCCACAACCGC |
Halberg R, et al. (1994): FT RO |
spoIVFAB | spoIVFA | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
spoVB | spoVB | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
spoVD | spoVD | SigE | Negative | 1584153..1584171 | -33:-21 | TTCTACCTGTCCAAATTCA |
Zhang B, et al. (1997): RO FT GS |
spoVD | spoVD | SigE | Negative | 1584177..1584193 | -9:+8 | AAAATGAAACAAGCCTA |
Zhang B, et al. (1997): RO FT GS |
murE-mraY-murD-spoVE-murG-murB-divIB-ylxWX-sbp | spoVE | SigE | Negative | 1590079..1590137 | -38:+21 | GGGAATACAACATGTCAAACGTGTCGATAATGTTGAACAAGCAGTATCTGCGGCGTTTG |
Eichenberger P, et al. (2004): FT AR |
murE-mraY-murD-spoVE-murG-murB-divIB-ylxWX-sbp | spoVE | SigE | Negative | 1590218..1590276 | -38:+21 | GGTGACATGTTTATAGATGCCGTGCATATGCTTAAGTAAGGGCTTGTCTTGAAGTAAAT |
Eichenberger P, et al. (2004): FT AR |
spoVK | spoVK | SigE | Positive | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
spoVM | spoVM | SigE | Positive | ND | ND | ND |
Levin PA, et al. (1993): DB RG |
yabMNOPQ-divIC-yabR | yabP | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
ybaN | ybaN | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
ycgFG | ycgF | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
yitE | yitE | SigE (?) | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
ykvUV | ykvU | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
ylbJ | ylbJ | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
ypjB | ypjB | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
yqfCD | yqfC | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
yqfZY | yqfZ | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
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