Transcription factor: |
Spo0A |
Factor type | LuxR/UhpA |
---|---|
SWISS-PROT | P06534 |
SubtiList | BG10765 |
Consensus seq. | TGNCGGAA |
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 which can be located downstream of the initiation site two adjacent boxes are often found these listed sites might be viewed in its complementary strand |
Promoter | Sigma | Regulation | Location | Binding seq.(cis-element) | Exp. | Author | Year |
---|---|---|---|---|---|---|---|
abrB-P2 | ND | Negative | +7:+34 | ATTTTGTCGAATAATGACGAAGAAAAAT | FT | Strauch M, et al. | 1990 |
spoIIG | sigA | positive | -86:-100 | TTGTCGAGGAAGTAT | SDM RO FT | Baldus JM, et al. | 1994 |
spoIIG | sigA | positive | -70:-85 | GGGAAATCTGCTTAAT | SDM RO FT | Baldus JM, et al. | 1994 |
spoIIA | sigH | positive | -72:-87 | CTTAAATTTTGTCCAG | FT | Baldus JM, et al. | 1994 |
spoIIA | sigH | positive | -28:-13 | TCATTCCGTCGAAATC | FT | Baldus JM, et al. | 1994 |
spo0F-P2 | sigH | Positive | -84:-51 | CAAAAGAGAAAATGCTCAGAAAATGTCGTAAAGTAGAC | DP SDM FT | Strauch MA, et al. | 1993 |
spo0F-P2 | sigH | Positive | +11:+53 | TTTGACGAAAATCATAATATTGGGGTGTAAAATGATGAATGAA | DP SDM FT | Strauch MA, et al. | 1993 |
spoIIE | sigA | Positive | -124:-118 | TAGACAA | SDM FT | York K, et al. | 1992 |
spoIIE | sigA | Positive | -103:-87 | TTTTCATAAACGAATAT | SDM FT | York K, et al. | 1992 |
spoIIE | sigA | Positive | -82:-66 | GCAGAAACCGTCGAAGA | SDM FT | York K, et al. | 1992 |
spoIIE | sigA | Positive | -48:-28 | CCTTCTTTTGACAAAATCCTA | SDM FT | York K, et al. | 1992 |
spo0A-Ps | sigH | Positive | -14:+1 | TTTGTCGAATGTAA | FT | Strauch MA, et al. | 1992 |
spo0A-Pv | ND | Negative | +38:+72 | AATTTCATTTTTAGTCGAAAAACAGAGAAAAACAT | FT | Strauch MA, et al. | 1992 |
spo0A-Pv | ND | Negative | +6:+20 | TTTTCGACAAATTCA | FT | Strauch MA, et al. | 1992 |
kinC | sigA | Positive | -30:-13 | ATTATTTGTCGAAGAATG | GS FT | Kobayashi K, et al. | 1995 |
kinC | sigA | Negative | -12:-1 | GTACAATAAGTA | GS FT | Kobayashi K, et al. | 1995 |
abrB-P2 | ND | Negative | +7:+34 | ATTTTGTCGAATAATGACGAAGAAAAAT | FT | Strauch M, et al. | 1990 |
spoIIG | sigA | positive | -24:-41 | TGGGAAAGTCTGTCAATT | SDM RO FT | Baldus JM, et al. | 1994 |
spoIIG | sigA | positive | -42:-53 | AATGTTGAGAGG | SDM RO FT | Baldus JM, et al. | 1994 |
spoIIA | sigH | positive | -71:-52 | TAATTATGCCGAATGACCAC | FT | Baldus JM, et al. | 1994 |
spoIIA | sigH | positive | -51:-33 | TAGTTTTGTCACGGTGAAG | FT | Baldus JM, et al. | 1994 |
dltA | sigA | Positive | ND | TTGTCGAAAAAACGGGAAGGGAATTT | DB FT | Perego M, et al. | 1995 |
kinA | ND | Negative | Hoch Two-component signal transduction ASM Press p129-144 | 1995 |