Factor type | Unique (DeoR family) |
---|---|
SWISS-PROT | P15281 |
SubtiList | BG10408 |
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 & Similar conserved hexameric motifs |
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 | 29725..29754 | -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 | 29795..29815 | +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 | 1904446..1904516 | -86:-16 | TCTTTTTCTATCATTTGGACAGCCCTTTTTTCCTTCTATGATTTTAACTGTCCAAGCCGCAAAATCTACTC |
Ichikawa H, et al. (2000): GS FT |
cotD | cotD | SigK | Negative | 2332298..2332318 | -79:-59 | AAAGACAGCTTAATTGCACAC |
Halberg R, et al. (1994): FT RO |
cotD | cotD | SigK | Negative | 2332260..2332279 | -40:-21 | CATCAGAACATGTACCCCTT |
Halberg R, et al. (1994): FT RO |
cotD | cotD | SigK | Negative | 2332161..2332186 | +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 | 755166..755195 | -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 | 1250513..1250542 | -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 | 3776807..3776867 | -60:+1 | ATAAAGTTTCTGTCCAAAACGAGAGTCATATTAGCTTGTCCCTGCCCATAGACTAGACTAG |
Eichenberger P, et al. (2004): FT GS AR |
yqhV-spoIIIAABCDEFGH | spoIIIAA | SigE | Negative | 2536875..2536929 | -54:+1 | CATAAATAAAGAGAGGCTTGTCATAAAGTCTGCCTCACATCATACATTTTAAAGA |
Eichenberger P, et al. (2004): FT AR |
spoIVA | spoIVA | SigE | Negative | ND | ND | ND |
Eichenberger P, et al. (2004): GS AR |
spoIVCA | spoIVCA | SigE | Positive | 2654223..2654256 | -47:-12 | TTAAAATCTCCTCATTTGGACAAACAGCTGTTAC |
Halberg R, et al. (1994): FT RO Eichenberger P, et al. (2004): GS AR |
spoIVCA | spoIVCA | SigE | Positive | 2654057..2654074 | +137:+154 | CGACCGAGGAACAAGCGA |
Halberg R, et al. (1994): FT RO Eichenberger P, et al. (2004): GS AR |
spoIVCB-spoIIIC | spoIVCB | SigE | Positive | 2652144..2652164 | -36:-16 | TACAGACACAGACAGCCTCCC |
Halberg R, et al. (1994): FT RO |
spoIVCB-spoIIIC | spoIVCB | SigE | Positive | 2652257..2652279 | +78:+100 | TAAAGAGCTTGTCTTTTTAGTAT |
Halberg R, et al. (1994): FT RO |
spoIVCB-spoIIIC | spoIVCB | SigE | Positive | 2652288..2652312 | +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 | 1583457..1583475 | -33:-21 | TTCTACCTGTCCAAATTCA |
Zhang B, et al. (1997): RO FT GS |
spoVD | spoVD | SigE | Negative | 1583481..1583497 | -9:+8 | AAAATGAAACAAGCCTA |
Zhang B, et al. (1997): RO FT GS |
murE-mraY-murD-spoVE-murG-murB-divIB-ylxWX-sbp | spoVE | SigE | Negative | 1589381..1589439 | -38:+21 | GGGAATACAACATGTCAAACGTGTCGATAATGTTGAACAAGCAGTATCTGCGGCGTTTG |
Eichenberger P, et al. (2004): FT AR |
murE-mraY-murD-spoVE-murG-murB-divIB-ylxWX-sbp | spoVE | SigE | Negative | 1589520..1589578 | -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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