DNA Binding Motif
Accessions: | SigA_2 (DBTBS 1.0) |
Names: | SigA_2 |
Organisms: | Bacillus subtilis |
Libraries: | DBTBS 1.0 1 1 Sierro N, Makita Y, de Hoon M, Nakai K. DBTBS: a database of transcriptional regulation in Bacillus subtilis containing upstream intergenic conservation information. Nucleic acids research 36:D93-6 (2008). [Pubmed] |
Length: | 6 |
Consensus: | TAtAAT |
Weblogo: | |
PSSM: | P0 A C G T 01 0 0.08 0 0.92 T 02 0.95 0 0 0.05 A 03 0.08 0.24 0 0.67 t 04 0.82 0 0.14 0.04 A 05 0.74 0.22 0.04 0 A 06 0.05 0 0.01 0.94 T |
Binding TFs: | SigA (Sigma-70 factor, region 1.2, Sigma-70 factor, region 1.1, Sigma-70 region 3, Sigma-70 region 2 , Sigma-70, region 4) |
Binding Sites: | abnA_2 abrB_2 abrB_3 ackA_3 acsA_2 acuA_2 adaA_1 addB_3 ahpC_2 ald alkA_2 alsS_1 amhX amyE_2 ansA_1 antE aprE_7 aprX_2 araA_4 araE_4 araR_2 arfM_2 argC_4 arsR_2 asd_1 bglC bglP_3 bglS_3 blt_3 bmr_3 bsrB ccdA ccpC_3 cdd_1 cggR_2 citA_1 citB_4 citG_1 citG_2 citM_4 citR citZ_4 clpE_6 clpE_7 clpP_2 clpX_1 codV comA comC_3 comEA_3 comFA_3 comGA_3 comK_6 comQ csbA_1 cspB_2 cssR_2 cssR_3 ctaA_3 ctsR_2 cydA_3 cymR cysH cysK_1 dctP_2 degQ_2 degS des_2 dhbA_2 divIB dnaA_10 dnaJ dppA_3 dra_3 drm_1 drm_2 ezrA_1 ezrA_2 fabHA_1 fabL_1 fabL_2 fapR_1 fbp feuA_2 flgB_1 fnr_2 ftsA_3 ftsA_4 ftsH fur_2 gabP_1 gabP_2 gabR_1 gabT_1 galE gapB_2 gcaD ggaA glnR_3 glpD_2 glpF_3 glpQ_2 glpT_2 gltA_4 gltC_2 gltR_3 gltX glyA_2 gntR_3 gntZ_1 groES_2 gtaB_1 guaA guaD_2 gudB gutB_2 gyrA hbs_2 hbs_3 hemA_3 hemZ_1 hmp_2 hrcA_2 htpG_1 htrA_2 hutP_5 icd ilvB_3 infC_2 iolR_3 ispA_1 kdgR_1 kinB_2 kinC_1 ldh_1 lepA liaG licB_2 licR lmrA_2 lonA_1 lonA_2 lrpC_2 lysC lytA_1 lytE_2 lytR_1 maeN_1 malA_2 mecA med_1 med_2 menB menE menF mmsA_4 mrgA_2 mta_2 mtrA nadB_1 nadE_1 narG_2 narK_2 nasA_2 nasB_2 nfrA_1 nifS_1 nrgA_1 nusA odhA ogt opuAA_1 opuAA_2 opuBA opuE_1 pabB pbpD pbpF pckA_2 pdhA pdhC perR_3 pgk pheS_1 phoA_2 phoB_3 phoD_2 phoP_6 phoP_7 phoP_8 phrE_1 phrI_1 pmi ppiB pssA_1 pssA_2 pstS_2 pta_3 ptsG_1 ptsH pucA_1 pucH_2 pucJ_2 purA_2 purE_2 purT pyrG pyrR_3 qcrA_1 rapA_2 rapB rapC_2 rapD_1 rapG_2 rapH_4 rbsR_4 recA_6 resA_2 resD_2 rocR_2 rpmH_1 rpmH_2 rpoB rpoE rpsD rrnA-16S_1 rrnA-16S_2 rrnB-16S_1 rrnB-16S_2 rrnD-16S_1 rrnD-16S_2 rrnO-16S_1 rrnO-16S_2 rsbR sacB_3 sacP_3 sacX_4 sboA_1 scr sda_3 sdhC secA sigD sigH_2 sigM_1 sigX_1 sinI_4 sinI_5 sinR sipS_2 speD speE spo0A_1 spo0A_2 spo0B spo0E_2 spo0F_1 spoIIE_1 spoIIGA_1 spoIIIE spoIIIJ srfAA_5 ssuB_1 tagA_4 tagD_4 tetL thrS_1 thrZ_1 treP_2 trnD-Asn trnD-Leu2 trpE_1 trxA_1 tuaA_2 tyrS_1 ureA_4 uxaC_3 valS_1 veg wapA_3 xpt_2 xsa_3 xylA_2 xynA xynP_2 yaaA yaaB yaaJ ybcO_1 ybgJ_2 yccC_1 ycdH_1 yceC_1 yciA_1 yciC_1 yczA_1 ydfJ_2 ydfK_1 ydjK_2 yfkJ_1 yflG yfmP yhaG_1 yhcL_1 yhcY_1 yhfL_2 yhjL_1 yjbD_2 yjcI yklA_2 ykoL_2 ykrT ykrU ykrV ykrW_1 ykrW_2 ykuF_2 ykuN_3 ykvW_2 ylaC_1 ylxM ymaA_2 yneI yneJ yocH_1 ypuE yqdB yqxD_1 yqxD_2 yqxM_1 yrrT_1 ysiA_2 ytkD_1 ytlI_2 ytlI_3 ytmI_3 ytrA_1 yurH_2 yusL_2 yuxH_1 yvbA_1 yveK_1 yvgR_2 yvqI_2 ywbI ywcJ_1 ywfK_2 ywjF_2 ywkA_1 ywoE_2 yxeK_1 yydF |
Publications: | Huang X, Helmann J.D. Identification of target promoters for the Bacillus subtilis sigma X factor using a consensus-directed search. Journal of molecular biology 279:165-73 (1998). [Pubmed] Raposo M.P, Inácio J.M, Mota L.J, de Sá-Nogueira I. Transcriptional regulation of genes encoding arabinan-degrading enzymes in Bacillus subtilis. Journal of bacteriology 186:1287-96 (2004). [Pubmed] Perego M, Spiegelman G.B, Hoch J.A. Structure of the gene for the transition state regulator, abrB: regulator synthesis is controlled by the spo0A sporulation gene in Bacillus subtilis. Molecular microbiology 2:689-99 (1988). [Pubmed] Grundy F.J, Waters D.A, Allen S.H, Henkin T.M. Regulation of the Bacillus subtilis acetate kinase gene by CcpA. Journal of bacteriology 175:7348-55 (1993). [Pubmed] Grundy F.J, Turinsky A.J, Henkin T.M. Catabolite regulation of Bacillus subtilis acetate and acetoin utilization genes by CcpA. Journal of bacteriology 176:4527-33 (1994). [Pubmed] Morohoshi F, Hayashi K, Munkata N. Bacillus subtilis alkA gene encoding inducible 3-methyladenine DNA glycosylase is adjacent to the ada operon. Journal of bacteriology 175:6010-7 (1993). [Pubmed] Haijema B.J, Hamoen L.W, Kooistra J, Venema G, van Sinderen D. Expression of the ATP-dependent deoxyribonuclease of Bacillus subtilis is under competence-mediated control. Molecular microbiology 15:203-11 (1995). [Pubmed] Antelmann H, Engelmann S, Schmid R, Hecker M. General and oxidative stress responses in Bacillus subtilis: cloning, expression, and mutation of the alkyl hydroperoxide reductase operon. Journal of bacteriology 178:6571-8 (1996). [Pubmed] Siranosian K.J, Ireton K, Grossman A.D. Alanine dehydrogenase (ald) is required for normal sporulation in Bacillus subtilis. Journal of bacteriology 175:6789-96 (1993). [Pubmed] Renna M.C, Najimudin N, Winik L.R, Zahler S.A. Regulation of the Bacillus subtilis alsS, alsD, and alsR genes involved in post-exponential-phase production of acetoin. Journal of bacteriology 175:3863-75 (1993). [Pubmed] Reents H, Münch R, Dammeyer T, Jahn D, Härtig E. The Fnr regulon of Bacillus subtilis. Journal of bacteriology 188:1103-12 (2006). [Pubmed] Kempf B, Bremer E. A novel amidohydrolase gene from Bacillus subtilis cloning: DNA-sequence analysis and map position of amhX. FEMS microbiology letters 141:129-37 (1996). [Pubmed] Nicholson W.L, Park Y.K, Henkin T.M, Won M, Weickert M.J, Gaskell J.A, Chambliss G.H. Catabolite repression-resistant mutations of the Bacillus subtilis alpha-amylase promoter affect transcription levels and are in an operator-like sequence. Journal of molecular biology 198:609-18 (1987). [Pubmed] Sun D.X, Setlow P. Cloning, nucleotide sequence, and expression of the Bacillus subtilis ans operon, which codes for L-asparaginase and L-aspartase. Journal of bacteriology 173:3831-45 (1991). [Pubmed] Wang L.F, Park S.S, Doi R.H. A novel Bacillus subtilis gene, antE, temporally regulated and convergent to and overlapping dnaE. Journal of bacteriology 181:353-6 (1999). [Pubmed] Henner D.J, Ferrari E, Perego M, Hoch J.A. Location of the targets of the hpr-97, sacU32(Hy), and sacQ36(Hy) mutations in upstream regions of the subtilisin promoter. Journal of bacteriology 170:296-300 (1988). [Pubmed] Ferrari E, Henner D.J, Perego M, Hoch J.A. Transcription of Bacillus subtilis subtilisin and expression of subtilisin in sporulation mutants. Journal of bacteriology 170:289-95 (1988). [Pubmed] Park S.S, Wong S.L, Wang L.F, Doi R.H. Bacillus subtilis subtilisin gene (aprE) is expressed from a sigma A (sigma 43) promoter in vitro and in vivo. Journal of bacteriology 171:2657-65 (1989). [Pubmed] Valbuzzi A, Ferrari E, Albertini A.M. A novel member of the subtilisin-like protease family from Bacillus subtilis. Microbiology (Reading, England) 145 ( Pt 11):3121-7 (1999). [Pubmed] Sá-Nogueira I, Nogueira T.V, Soares S, de Lencastre H. The Bacillus subtilis L-arabinose (ara) operon: nucleotide sequence, genetic organization and expression. Microbiology (Reading, England) 143 ( Pt 3):957-69 (1997). [Pubmed] Sá-Nogueira I, Ramos S.S. Cloning, functional analysis, and transcriptional regulation of the Bacillus subtilis araE gene involved in L-arabinose utilization. Journal of bacteriology 179:7705-11 (1997). [Pubmed] Marino M, Ramos H.C, Hoffmann T, Glaser P, Jahn D. Modulation of anaerobic energy metabolism of Bacillus subtilis by arfM (ywiD). Journal of bacteriology 183:6815-21 (2001). [Pubmed] Cruz Ramos H, Boursier L, Moszer I, Kunst F, Danchin A, Glaser P. Anaerobic transcription activation in Bacillus subtilis: identification of distinct FNR-dependent and -independent regulatory mechanisms. The EMBO journal 14:5984-94 (1995). [Pubmed] Smith M.C, Mountain A, Baumberg S. Sequence analysis of the Bacillus subtilis argC promoter region. Gene 49:53-60 (1986). [Pubmed] O'Reilly M, Woodson K, Dowds B.C, Devine K.M. The citrulline biosynthetic operon, argC-F, and a ribose transport operon, rbs, from Bacillus subtilis are negatively regulated by Spo0A. Molecular microbiology 11:87-98 (1994). [Pubmed] Sato T, Kobayashi Y. The ars operon in the skin element of Bacillus subtilis confers resistance to arsenate and arsenite. Journal of bacteriology 180:1655-61 (1998). [Pubmed] Chen N.Y, Jiang S.Q, Klein D.A, Paulus H. Organization and nucleotide sequence of the Bacillus subtilis diaminopimelate operon, a cluster of genes encoding the first three enzymes of diaminopimelate synthesis and dipicolinate synthase. The Journal of biological chemistry 268:9448-65 (1993). [Pubmed] Robson L.M, Chambliss G.H. Endo-beta-1,4-glucanase gene of Bacillus subtilis DLG. Journal of bacteriology 169:2017-25 (1987). [Pubmed] Le Coq D, Lindner C, Krüger S, Steinmetz M, Stülke J. New beta-glucoside (bgl) genes in Bacillus subtilis: the bglP gene product has both transport and regulatory functions similar to those of BglF, its Escherichia coli homolog. Journal of bacteriology 177:1527-35 (1995). [Pubmed] Steinmetz M, Aymerich S. [Genetic analysis of sacR, a cis-regulator of levan-saccharase synthesis of Bacillus subtilis]. Annales de l'Institut Pasteur. Microbiologie 137A:3-14 (). [Pubmed] Schnetz K, Stülke J, Gertz S, Krüger S, Krieg M, Hecker M, Rak B. LicT, a Bacillus subtilis transcriptional antiterminator protein of the BglG family. Journal of bacteriology 178:1971-9 (1996). [Pubmed] Baranova N.N, Danchin A, Neyfakh A.A. Mta, a global MerR-type regulator of the Bacillus subtilis multidrug-efflux transporters. Molecular microbiology 31:1549-59 (1999). [Pubmed] Ando Y, Asari S, Suzuma S, Yamane K, Nakamura K. Expression of a small RNA, BS203 RNA, from the yocI-yocJ intergenic region of Bacillus subtilis genome. FEMS microbiology letters 207:29-33 (2002). [Pubmed] Schiött T, Hederstedt L. Efficient spore synthesis in Bacillus subtilis depends on the CcdA protein. Journal of bacteriology 182:2845-54 (2000). [Pubmed] Kim H.J, Jourlin-Castelli C, Kim S.I, Sonenshein A.L. Regulation of the bacillus subtilis ccpC gene by ccpA and ccpC. Molecular microbiology 43:399-410 (2002). [Pubmed] Wang P.Z, Doi R.H. Overlapping promoters transcribed by bacillus subtilis sigma 55 and sigma 37 RNA polymerase holoenzymes during growth and stationary phases. The Journal of biological chemistry 259:8619-25 (1984). [Pubmed] Song B.H, Neuhard J. Chromosomal location, cloning and nucleotide sequence of the Bacillus subtilis cdd gene encoding cytidine/deoxycytidine deaminase. Molecular & general genetics : MGG 216:462-8 (1989). [Pubmed] Ludwig H, Homuth G, Schmalisch M, Dyka F.M, Hecker M, Stülke J. Transcription of glycolytic genes and operons in Bacillus subtilis: evidence for the presence of multiple levels of control of the gapA operon. Molecular microbiology 41:409-22 (2001). [Pubmed] Jin S, Sonenshein A.L. Transcriptional regulation of Bacillus subtilis citrate synthase genes. Journal of bacteriology 176:4680-90 (1994). [Pubmed] Whipple F.W, Sonenshein A.L. Mechanism of initiation of transcription by Bacillus subtilis RNA polymerase at several promoters. Journal of molecular biology 223:399-414 (1992). [Pubmed] Feavers I.M, Price V, Moir A. The regulation of the fumarase (citG) gene of Bacillus subtilis 168. Molecular & general genetics : MGG 211:465-71 (1988). [Pubmed] Tatti K.M, Carter H.L, Moir A, Moran C.P. Sigma H-directed transcription of citG in Bacillus subtilis. Journal of bacteriology 171:5928-32 (1989). [Pubmed] Price V.A, Feavers I.M, Moir A. Role of sigma H in expression of the fumarase gene (citG) in vegetative cells of Bacillus subtilis 168. Journal of bacteriology 171:5933-9 (1989). [Pubmed] Yamamoto H, Murata M, Sekiguchi J. The CitST two-component system regulates the expression of the Mg-citrate transporter in Bacillus subtilis. Molecular microbiology 37:898-912 (2000). [Pubmed] Derré I, Rapoport G, Devine K, Rose M, Msadek T. ClpE, a novel type of HSP100 ATPase, is part of the CtsR heat shock regulon of Bacillus subtilis. Molecular microbiology 32:581-93 (1999). [Pubmed] Gerth U, Krüger E, Derré I, Msadek T, Hecker M. Stress induction of the Bacillus subtilis clpP gene encoding a homologue of the proteolytic component of the Clp protease and the involvement of ClpP and ClpX in stress tolerance. Molecular microbiology 28:787-802 (1998). [Pubmed] Gerth U, Wipat A, Harwood C.R, Carter N, Emmerson P.T, Hecker M. Sequence and transcriptional analysis of clpX, a class-III heat-shock gene of Bacillus subtilis. Gene 181:77-83 (1996). [Pubmed] Slack F.J, Serror P, Joyce E, Sonenshein A.L. A gene required for nutritional repression of the Bacillus subtilis dipeptide permease operon. Molecular microbiology 15:689-702 (1995). [Pubmed] Weinrauch Y, Guillen N, Dubnau D.A. Sequence and transcription mapping of Bacillus subtilis competence genes comB and comA, one of which is related to a family of bacterial regulatory determinants. Journal of bacteriology 171:5362-75 (1989). [Pubmed] van Sinderen D, ten Berge A, Hayema B.J, Hamoen L, Venema G. Molecular cloning and sequence of comK, a gene required for genetic competence in Bacillus subtilis. Molecular microbiology 11:695-703 (1994). [Pubmed] Mohan S, Dubnau D. Transcriptional regulation of comC: evidence for a competence-specific transcription factor in Bacillus subtilis. Journal of bacteriology 172:4064-71 (1990). [Pubmed] Hahn J, Inamine G, Kozlov Y, Dubnau D. Characterization of comE, a late competence operon of Bacillus subtilis required for the binding and uptake of transforming DNA. Molecular microbiology 10:99-111 (1993). [Pubmed] Londoño-Vallejo J.A, Dubnau D. comF, a Bacillus subtilis late competence locus, encodes a protein similar to ATP-dependent RNA/DNA helicases. Molecular microbiology 9:119-31 (1993). [Pubmed] Kong L, Siranosian K.J, Grossman A.D, Dubnau D. Sequence and properties of mecA, a negative regulator of genetic competence in Bacillus subtilis. Molecular microbiology 9:365-73 (1993). [Pubmed] Albano M, Breitling R, Dubnau D.A. Nucleotide sequence and genetic organization of the Bacillus subtilis comG operon. Journal of bacteriology 171:5386-404 (1989). [Pubmed] Weinrauch Y, Msadek T, Kunst F, Dubnau D. Sequence and properties of comQ, a new competence regulatory gene of Bacillus subtilis. Journal of bacteriology 173:5685-93 (1991). [Pubmed] Boylan S.A, Thomas M.D, Price C.W. Genetic method to identify regulons controlled by nonessential elements: isolation of a gene dependent on alternate transcription factor sigma B of Bacillus subtilis. Journal of bacteriology 173:7856-66 (1991). [Pubmed] Willimsky G, Bang H, Fischer G, Marahiel M.A. Characterization of cspB, a Bacillus subtilis inducible cold shock gene affecting cell viability at low temperatures. Journal of bacteriology 174:6326-35 (1992). [Pubmed] Darmon E, Noone D, Masson A, Bron S, Kuipers O.P, Devine K.M, van Dijl J.M. A novel class of heat and secretion stress-responsive genes is controlled by the autoregulated CssRS two-component system of Bacillus subtilis. Journal of bacteriology 184:5661-71 (2002). [Pubmed] Paul S, Zhang X, Hulett F.M. Two ResD-controlled promoters regulate ctaA expression in Bacillus subtilis. Journal of bacteriology 183:3237-46 (2001). [Pubmed] Sun G, Sharkova E, Chesnut R, Birkey S, Duggan M.F, Sorokin A, Pujic P, Ehrlich S.D, Hulett F.M. Regulators of aerobic and anaerobic respiration in Bacillus subtilis. Journal of bacteriology 178:1374-85 (1996). [Pubmed] Krüger E, Msadek T, Hecker M. Alternate promoters direct stress-induced transcription of the Bacillus subtilis clpC operon. Molecular microbiology 20:713-23 (1996). [Pubmed] Winstedt L, Yoshida K, Fujita Y, von Wachenfeldt C. Cytochrome bd biosynthesis in Bacillus subtilis: characterization of the cydABCD operon. Journal of bacteriology 180:6571-80 (1998). [Pubmed] Choi S.Y, Reyes D, Leelakriangsak M, Zuber P. The global regulator Spx functions in the control of organosulfur metabolism in Bacillus subtilis. Journal of bacteriology 188:5741-51 (2006). [Pubmed] Mansilla M.C, Albanesi D, de Mendoza D. Transcriptional control of the sulfur-regulated cysH operon, containing genes involved in L-cysteine biosynthesis in Bacillus subtilis. Journal of bacteriology 182:5885-92 (2000). [Pubmed] van der Ploeg J.R, Barone M, Leisinger T. Functional analysis of the Bacillus subtilis cysK and cysJI genes. FEMS microbiology letters 201:29-35 (2001). [Pubmed] Even S, Burguière P, Auger S, Soutourina O, Danchin A, Martin-Verstraete I. Global control of cysteine metabolism by CymR in Bacillus subtilis. Journal of bacteriology 188:2184-97 (2006). [Pubmed] Asai K, Baik S.H, Kasahara Y, Moriya S, Ogasawara N. Regulation of the transport system for C4-dicarboxylic acids in Bacillus subtilis. Microbiology (Reading, England) 146 ( Pt 2):263-71 (2000). [Pubmed] Yang M, Ferrari E, Chen E, Henner D.J. Identification of the pleiotropic sacQ gene of Bacillus subtilis. Journal of bacteriology 166:113-9 (1986). [Pubmed] Msadek T, Kunst F, Henner D, Klier A, Rapoport G, Dedonder R. Signal transduction pathway controlling synthesis of a class of degradative enzymes in Bacillus subtilis: expression of the regulatory genes and analysis of mutations in degS and degU. Journal of bacteriology 172:824-34 (1990). [Pubmed] Aguilar P.S, Lopez P, de Mendoza D. Transcriptional control of the low-temperature-inducible des gene, encoding the delta5 desaturase of Bacillus subtilis. Journal of bacteriology 181:7028-33 (1999). [Pubmed] Baichoo N, Wang T, Ye R, Helmann J.D. Global analysis of the Bacillus subtilis Fur regulon and the iron starvation stimulon. Molecular microbiology 45:1613-29 (2002). [Pubmed] Rowland B.M, Taber H.W. Duplicate isochorismate synthase genes of Bacillus subtilis: regulation and involvement in the biosyntheses of menaquinone and 2,3-dihydroxybenzoate. Journal of bacteriology 178:854-61 (1996). [Pubmed] Harry E.J, Rowland S.L, Malo M.S, Wake R.G. Expression of divIB of Bacillus subtilis during vegetative growth. Journal of bacteriology 176:1172-9 (1994). [Pubmed] Cao M, Helmann J.D. The Bacillus subtilis extracytoplasmic-function sigmaX factor regulates modification of the cell envelope and resistance to cationic antimicrobial peptides. Journal of bacteriology 186:1136-46 (2004). [Pubmed] Moriya S, Fukuoka T, Ogasawara N, Yoshikawa H. Regulation of initiation of the chromosomal replication by DnaA-boxes in the origin region of the Bacillus subtilis chromosome. The EMBO journal 7:2911-7 (1988). [Pubmed] Ogasawara N, Moriya S, Yoshikawa H. Structure and function of the region of the replication origin of the Bacillus subtilis chromosome. IV. Transcription of the oriC region and expression of DNA gyrase genes and other open reading frames. Nucleic acids research 13:2267-79 (1985). [Pubmed] Homuth G, Masuda S, Mogk A, Kobayashi Y, Schumann W. The dnaK operon of Bacillus subtilis is heptacistronic. Journal of bacteriology 179:1153-64 (1997). [Pubmed] Slack F.J, Mueller J.P, Strauch M.A, Mathiopoulos C, Sonenshein A.L. Transcriptional regulation of a Bacillus subtilis dipeptide transport operon. Molecular microbiology 5:1915-25 (1991). [Pubmed] Saxild H.H, Andersen L.N, Hammer K. Dra-nupC-pdp operon of Bacillus subtilis: nucleotide sequence, induction by deoxyribonucleosides, and transcriptional regulation by the deoR-encoded DeoR repressor protein. Journal of bacteriology 178:424-34 (1996). [Pubmed] Schuch R, Garibian A, Saxild H.H, Piggot P.J, Nygaard P. Nucleosides as a carbon source in Bacillus subtilis: characterization of the drm-pupG operon. Microbiology (Reading, England) 145 ( Pt 10):2957-66 (1999). [Pubmed] Chung K.M, Hsu H.H, Govindan S, Chang B.Y. Transcription regulation of ezrA and its effect on cell division of Bacillus subtilis. Journal of bacteriology 186:5926-32 (2004). [Pubmed] Schujman G.E, Paoletti L, Grossman A.D, de Mendoza D. FapR, a bacterial transcription factor involved in global regulation of membrane lipid biosynthesis. Developmental cell 4:663-72 (2003). [Pubmed] Yamamoto H, Mori M, Sekiguchi J. Transcription of genes near the sspE locus of the Bacillus subtilis genome. Microbiology (Reading, England) 145 ( Pt 8):2171-80 (1999). [Pubmed] Schujman G.E, Guerin M, Buschiazzo A, Schaeffer F, Llarrull L.I, Reh G, Vila A.J, Alzari P.M, de Mendoza D. Structural basis of lipid biosynthesis regulation in Gram-positive bacteria. The EMBO journal 25:4074-83 (2006). [Pubmed] Fujita Y, Yoshida K, Miwa Y, Yanai N, Nagakawa E, Kasahara Y. Identification and expression of the Bacillus subtilis fructose-1, 6-bisphosphatase gene (fbp). Journal of bacteriology 180:4309-13 (1998). [Pubmed] Fuangthong M, Helmann J.D. Recognition of DNA by three ferric uptake regulator (Fur) homologs in Bacillus subtilis. Journal of bacteriology 185:6348-57 (2003). [Pubmed] West J.T, Estacio W, Márquez-Magaña L. Relative roles of the fla/che P(A), P(D-3), and P(sigD) promoters in regulating motility and sigD expression in Bacillus subtilis. Journal of bacteriology 182:4841-8 (2000). [Pubmed] Estacio W, Anna-Arriola S.S, Adedipe M, Márquez-Magaña L.M. Dual promoters are responsible for transcription initiation of the fla/che operon in Bacillus subtilis. Journal of bacteriology 180:3548-55 (1998). [Pubmed] Gonzy-Tréboul G, Karmazyn-Campelli C, Stragier P. Developmental regulation of transcription of the Bacillus subtilis ftsAZ operon. Journal of molecular biology 224:967-79 (1992). [Pubmed] Fukuchi K, Kasahara Y, Asai K, Kobayashi K, Moriya S, Ogasawara N. The essential two-component regulatory system encoded by yycF and yycG modulates expression of the ftsAZ operon in Bacillus subtilis. Microbiology (Reading, England) 146 ( Pt 7):1573-83 (2000). [Pubmed] Howell A, Dubrac S, Andersen K.K, Noone D, Fert J, Msadek T, Devine K. Genes controlled by the essential YycG/YycF two-component system of Bacillus subtilis revealed through a novel hybrid regulator approach. Molecular microbiology 49:1639-55 (2003). [Pubmed] Deuerling E, Paeslack B, Schumann W. 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