Factor type | LuxR/UhpA |
---|---|
SWISS-PROT | ND |
SubtiList | ND |
Consensus seq. | TGTCGAA |
Comment | a key bi-functional regulator to control developmental transcription activities. Increases its affinity after phosphorylation (phosphorelay system). Spo0F is required for the phosphorylation. Two-domain structure. Binding consensus is called 0A box and can be located downstream of the initiation site. Often, two adjacent boxes are found. These listed sites might be viewed in its complementary strand. |
Link to | Phylogenetic profile, Weight matrix & Motif alignment |
Operon | Regulated Gene | Sigma | Regulation | Absolute position | Location | Binding seq.(cis-element) | Experimental evidence |
---|---|---|---|---|---|---|---|
metS | metS | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
rapA-phrA | rapA | SigA | Negative | ND | ND | ND |
Mueller JP & Sonenshein AL (1992): DB RG Molle V, et al. (2003): GS CH |
abrB | abrB | SigA | Negative | 45174..45201 | +7:+34 | ATTTTGTCGAATAATGACGAAGAAAAAT |
Perego M & Hoch J (1988): Genetics and Biotechnology of Bacilli, Vol. 2, pp. 129-134: RG DB Strauch M, et al. (1990): FT Fujita M, et al. (2005): RG GS Molle V, et al. (2003): GS CH |
dltABCDE | dltA | SigX | Positive | 3952071..3952091 | +1:+21 | ATGTGATTGTCGAAAAAACGG |
Perego M, et al. (1995): DB FT |
cdd-era | era | None | Positive | ND | ND | ND |
Minkovsky N, et al. (2002): DB RG |
kinA | kinA | SigH | Negative | 1469981..1470001 | +13:+33 | ATCTGTATATGTCGAAACACG |
Fujita M, et al. (1998): GS |
kinC | kinC | SigA | Positive | 1518277..1518306 | -30:-1 | ATTATTTGTCGAAGAATGGTACAATAAGTA |
Kobayashi K, et al. (1995): GS FT |
sinIR | sinI | SigA | Positive | 2552271..2552298 | -50:-26 | ACCATTCGACATCATTCTCGTTTTTTTT |
Shafikhani SH, et al. (2002): PE FT |
spo0A | spo0A | SigH | Positive | 2518876..2518889 | -18:-5 | TTTGTCGAATGTAA |
Strauch MA, et al. (1992): FT |
spo0A | spo0A | SigA | Negative | 2518953..2518987 | +38:+72 | AATTTCATTTTTAGTCGAAAAACAGAGAAAAACAT |
Strauch MA, et al. (1992): FT |
spo0A | spo0A | SigA | Negative | 2519005..2519029 | -5:+20 | AAAAGAAGATTTTTCGACAAATTCA |
Strauch MA, et al. (1992): FT |
spo0F | spo0F | SigH | Positive | 3810012..3810049 | -84:-51 | CAAAAGAGAAAATGCTCAGAAAATGTCGTAAAGTAGAC |
Strauch MA, et al. (1993): DP SDM FT |
spo0F | spo0F | SigH | Positive | 3809913..3809955 | +11:+53 | TTTGACGAAAATCATAATATTGGGGTGTAAAATGATGAATGAA |
Strauch MA, et al. (1993): DP SDM FT |
dacF-spoIIAAB-sigF | spoIIAA | SigH | Positive | 2445038..2445053 | -28:-13 | TCATTCCGTCGAAATC |
Baldus JM, et al. (1994): FT Fujita M, et al. (2005): OV RG GS |
dacF-spoIIAAB-sigF | spoIIAA | SigH | Positive | 2445058..2445076 | -51:-33 | TAGTTTTGTCACGGTGAAG |
Baldus JM, et al. (1994): FT Fujita M, et al. (2005): OV RG GS |
dacF-spoIIAAB-sigF | spoIIAA | SigH | Positive | 2445077..2445096 | -71:-52 | TAATTATGCCGAATGACCAC |
Baldus JM, et al. (1994): FT Fujita M, et al. (2005): OV RG GS |
dacF-spoIIAAB-sigF | spoIIAA | SigH | Positive | 2445091..2445122 | -66:-97 | CGATGGGAGACTGGACAAAATTTAAGTAATTA |
Baldus JM, et al. (1994): FT Fujita M, et al. (2005): OV RG GS |
spoIIE | spoIIE | SigA | Positive | 70375..70401 | -134:-108 | TTTTCATTTTTAGACAACATTCCGGAA |
York K, et al. (1992): SDM FT Fujita M, et al. (2005): GS |
spoIIE | spoIIE | SigA | Positive | 70406..70422 | -103:-87 | TTTTCATAAACGAATAT |
York K, et al. (1992): SDM FT Fujita M, et al. (2005): GS |
spoIIE | spoIIE | SigA | Positive | 70427..70443 | -82:-66 | GCAGAAACCGTCGAAGA |
York K, et al. (1992): SDM FT Fujita M, et al. (2005): GS |
spoIIE | spoIIE | SigA | Positive | 70461..70481 | -48:-28 | CCTTCTTTTGACAAAATCCTA |
York K, et al. (1992): SDM FT Fujita M, et al. (2005): GS |
spoIIGA-sigE-sigG | spoIIGA | SigA | Positive | 1603634..1603648 | -100:-86 | ATACTTCCTCGACAA |
Baldus JM, et al. (1994): SDM RO FT Fujita M, et al. (2005): RG OV GS |
spoIIGA-sigE-sigG | spoIIGA | SigA | Positive | 1603649..1603664 | -85:-70 | ATTAAGCAGATTTCCC |
Baldus JM, et al. (1994): SDM RO FT Fujita M, et al. (2005): RG OV GS |
spoIIGA-sigE-sigG | spoIIGA | SigA | Positive | 1603679..1603696 | -55:-38 | TTCCTCTCAACATTAATT |
Baldus JM, et al. (1994): SDM RO FT Fujita M, et al. (2005): RG OV GS |
spoIIGA-sigE-sigG | spoIIGA | SigA | Positive | 1603693..1603710 | -41:-24 | AATTGACAGACTTTCCCA |
Baldus JM, et al. (1994): SDM RO FT Fujita M, et al. (2005): RG OV GS |
skf | ybcO | SigA | Positive | 213824..213891 | -64:+4 | AATTTTTAGGATAATATACAAAATCCCCCTTACTTCGACAATTGCAATCTGGTATTATCGTATCGCAT |
Molle V, et al. (2003): GS CH Fujita M, et al. (2005): RG OV, gfp fusion, GS Chen G, et al. (2006): FT, binding site mutation |
yqxM-sipW-tasA | yqxM | SigH | Positive | ND | ND | ND |
Stover AG & Driks A (1999): Western blot Stover AG & Driks A (1999): RG |
yuxH | yuxH | SigA | Negative | 3259283..3259348 | -49:+17 | TTTTCATGTTTAGACAATTTTCGTCAAATTATTTGATATACTTAGGGGTGAAAGCCGCGCGTATTG |
Fujita M, et al. (2005): RG Molle V, et al. (2003): CH GS |
sdp | yvaW | None | Negative | ND | ND | ND |
Fujita M, et al. (2005): OV RG GS Molle V, et al. (2003): CH GS |
racA | ywkC | SigH | Positive | ND | ND | ND |
Ben-Yehuda S, et al. (2003): DB RG Wu LJ & Errington J (2003): DB Western blot Molle V, et al. (2003): GS CH Fujita M, et al. (2005): RG OV |
yxbCD | yxbC | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yppDE | yppD | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yppF | yppF | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yttP | yttP | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yocH | yocH | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yneEF | yneE | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yfmIJ | yfmI | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yusED | yusE | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ycgMN | ycgM | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yqcGF | yqcG | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yqxIJ | yqxI | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yerBC | yerB | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
accDA | accD | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ykuJK-ykzF-ykuL-ccpC | ykzF | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ykuJK-ykzF-ykuL-ccpC | ykuL | None | Positive | ND | ND | ND |
Molle V, et al. (2003): GS CH |
tkt | tkt | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yqzDC | yqzD | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
med-comZ | med | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yrrL | yrrL | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ftsEX | ftsE | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
fla-che | flgB | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
lytE | lytE | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ykaA-pit | ykaA | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
fruRKA | fruR | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
cotD | cotD | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
divIVA | divIVA | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
rocDEF | rocD | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yvyE-yvhJ | yvyE | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
nfrA-ywcH | nfrA | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
nfrA-ywcH | ywcH | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
soj-spo0J | soj | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
rok | rok | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
dnaAN | dnaA | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yqxD-dnaG-sigA | dnaG | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yaaDE | yaaD | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ylmDEFGH | ylmD | None | Negative | ND | ND | ND |
Molle V, et al. (2003): GS CH |
comK | comK | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yvyD | yvyD | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
spoIID | spoIID | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
veg | veg | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ygaO | ygaO | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
yjcPQ | yjcP | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
rocG | rocG | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
ywqCD | ywqC | None | None | ND | ND | ND |
Molle V, et al. (2003): GS CH |
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