Transcription factor: |
CcpA |
Factor type | LacI family |
---|---|
SWISS-PROT | P25144 |
SubtiList | BG10376 |
Consensus seq. | WTGNAANCGNWNNCW |
Comment | also called AlsA common repressor in catabolite repression (CR) but may act as a positive regulator of genes involved in excretion of excess carbon its binding site is called CRE CR is reviewed in Saier, M.H., et al, 1996 (97086502) and Hueck, C.J. and Hillen, W., 1995 (95302950) it binds to fructose-1,6-bisphosphate and HPr |
Promoter | Sigma | Regulation | Location | Binding seq.(cis-element) | Exp. | Author | Year |
---|---|---|---|---|---|---|---|
acuA | ND | Negative | -33:-20 | TGAAAACGCTTTAT | DB SDM | Grundy FJ, et al. | 1994 |
acsA | ND | Negative | +38:+51 | TGAAAGCGTTACCA | DB SDM | Grundy FJ, et al. | 1994 |
mmgA | sigE | Negative | +15:+28 | TGTAAGCGCTGTCT | SDM DB | Bryan EM, et al. | 1996 |
amyE | ND | Negative | -7:+17 | TAAATGTAAGCGTTAACAAAATTC | GS FT | Kim JH, et al. | 1995 |
hutP | ND | Negative | +2:+15 | GTTAATAGTTATCA | SDM DP | Wray LV Jr, et al. | 1994 |
hutP | ND | Negative | +203:+216 | TGAAACCGCTTCCA | SDM DP | Wray LV Jr, et al. | 1994 |
gntR | ND | Negative | +142:+155 | TGAAAGCGGTACCA | SDM S1 HB | Miwa Y, et al. | 1993 |
xylA | ND | Negative | +134:+147 | TGGAAGCGTAAACA | SDM | Kraus A,et al. | 1994 |
licS | ND | Negative | No data | AGAAAACGCTTTCA | SDM DB | Kruger S, et al. | 1993 |
ackA | ND | Positive | -124:-110 | TGTAAGCGTTCATCA | DB DP | Grundy FJ, et al. | 1993 |
ackA | ND | Positive | -64:-51 | TGTAAGCGTTATCA | DB DP | Grundy FJ, et al. | 1993 |
bglP | ND | Negative | -43:-30 | TGAAAGCGTTGACA | RO DP | Kruger S, et al. | 1996 |
rbsR | sigA | Negative | -1:+13 | TGTAAACGGTTACA | PE | Woodson K, et al. | 1994 |
levD | sigL | Negative | -50:-36 | TGAAAACGCTTAACA | SDM DB | Martin-Verstraete I, et al. | 1995 |
licB | ND | Negative | -29:-16 | TGAAAGCGATTTCA | HM | Tobisch S, et al. | 1997 |
xynC | ND | Negative | No data | TGTTTGATC-AACA | DB HB HM | Lindner C, et al. | 1994 |
alsS | ND | Positive? | No data | unknown | DB | Renna MC, et al. | 1993 |
msmX | ND | Negative | -24:+38 | TATAAGAAAGCGTTTACAATAAC | beta-gal | Miwa Y et al. | 2000 |
yxkJ | ND | Negative | -29:+45 | CAATTGCAAACGGATACAATTCA | beta-gal | Miwa Y et al. | 2000 |
iolB | ND | Negative | -22:+34 | GAAATGAAAACGTTGTCATCGTT | beta-gal | Miwa Y et al. | 2000 |
ydbH | ND | Negative | -30:+48 | TGTATGAAAACGCTATCATTCTA | beta-gal | Miwa Y et al. | 2000 |
galT | ND | Negative | -36:+50 | CGAATGGAAGCGGATACAGATAC | beta-gal | Miwa Y et al. | 2000 |
citM | ND | Negative | -22:+49 | AAAATGTAAGCGGATTCATTTAA | beta-gal | Miwa Y et al. | 2000 |
yjmA | ND | Negative | -21:+38 | CAAATGAAAGCGTTATCAAATGT | beta-gal | Miwa Y et al. | 2000 |
ydhO | ND | Negative | -35:+41 | GACTTGGAAGCGGTATCATTCCA | beta-gal | Miwa Y et al. | 2000 |
acoA | ND | Negative | -36:+47 | AAAATGTAAGCGTTTGCTTTTTC | beta-gal | Miwa Y et al. | 2000 |
araB | ND | Negative | -36:+50 | TCAATGAAAACGATTACAAAGGA | beta-gal | Miwa Y et al. | 2000 |
lcfA | ND | Negative | -32:+58 | AAAATGAAAACGTTATCAATAGT | beta-gal | Miwa Y et al. | 2000 |
dra | ND | Negative | -31:+43 | GCTTTGAAACCGCATACACAAAA | beta-gal | Miwa Y et al. | 2000 |
kdgA | ND | Negative | -21:+37 | ATTATGGAAGCGCTGACATTCGG | beta-gal | Miwa Y et al. | 2000 |
yobO | ND | Negative | -33:+45 | TTAATGTAAGCGGATTCACAGCG | beta-gal | Miwa Y et al. | 2000 |
treP | ND | Negative | -22:+46 | GCTGTGAAAACGCTTGCAGATAT | beta-gal | Miwa Y et al. | 2000 |
gntR | ND | Negative | -31:+50 | TGATTGAAAGCGGTACCATTTTA | beta-gal | Miwa Y et al. | 2000 |
yxjC | ND | Negative | -19:+35 | TTTTTGTAAACGCTTTCTAGTTC | beta-gal | Miwa Y et al. | 2000 |