| 99777 |
cd06170 |
LuxR_C_like |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-helix motif and binds DNA. Proteins belonging to this group are response regulators; some act as transcriptional activators, others as transcriptional repressors. Many are active as homodimers. Many are two domain proteins in which the DNA binding property of the C-terminal DNA binding domain is modulated by modifications of the N-terminal domain. For example in the case of Lux R which participates in the regulation of gene expression in response to fluctuations in cell-population density (quorum-sensing), a signaling molecule, the pheromone Acyl HSL (N-acyl derivatives of homoserine lactone), binds to the N-terminal domain and leads to LuxR dimerization. For others phophorylation of the N-terminal domain leads to multimerization, for example Escherichia coli NarL and Sinorhizobium melilot FixJ. NarL controls gene expression of many respiratory-related operons when environmental nitrate or nitrite is present under anerobic conditions. FixJ is involved in the transcriptional activation of nitrogen fixation genes. The group also includes small proteins which lack an N-terminal signaling domain, such as Bacillus subtilis GerE. GerE is dimeric and acts in conjunction with sigmaK as an activator or a repressor modulating the expression of various genes in particular those encoding the spore-coat. These LuxR family regulators may share a similar organization of their target binding sites. For example the LuxR dimer binds the lux box, a 20bp inverted repeat, GerE dimers bind two 12bp consensus sequences in inverted orientation having the central four bases overlap, and the NarL dimer binds two 7bp inverted repeats separated by 2 bp. |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-... |
true |
false |
true |
57 |
2e-15 |
79.50 |
100.00 |
1,459,0,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAID 516
cd06170 1 LTPREREVLRLLAEGKTNKEIADILGISEKTVKTHLRNIMRKLGVKSRTQLVAYAIR 57
|
|
cl10457 |
142561 |
LuxR_C_like |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-helix motif and binds DNA. Proteins belonging to this group are response regulators; some act as transcriptional activators, others as transcriptional repressors. Many are active as homodimers. Many are two domain proteins in which the DNA binding property of the C-terminal DNA binding domain is modulated by modifications of the N-terminal domain. For example in the case of Lux R which participates in the regulation of gene expression in response to fluctuations in cell-population density (quorum-sensing), a signaling molecule, the pheromone Acyl HSL (N-acyl derivatives of homoserine lactone), binds to the N-terminal domain and leads to LuxR dimerization. For others phophorylation of the N-terminal domain leads to multimerization, for example Escherichia coli NarL and Sinorhizobium melilot FixJ. NarL controls gene expression of many respiratory-related operons when environmental nitrate or nitrite is present under anerobic conditions. FixJ is involved in the transcriptional activation of nitrogen fixation genes. The group also includes small proteins which lack an N-terminal signaling domain, such as Bacillus subtilis GerE. GerE is dimeric and acts in conjunction with sigmaK as an activator or a repressor modulating the expression of various genes in particular those encoding the spore-coat. These LuxR family regulators may share a similar organization of their target binding sites. For example the LuxR dimer binds the lux box, a 20bp inverted repeat, GerE dimers bind two 12bp consensus sequences in inverted orientation having the central four bases overlap, and the NarL dimer binds two 7bp inverted repeats separated by 2 bp. |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-... |
0 |
| 28958 |
cd00077 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
true |
false |
true |
145 |
4e-09 |
58.17 |
90.34 |
1,281,0,131 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 282 PFTLGHSRGVANLVAGAARHLGMSPSDITHLYRAGLVHSLGKMGVSNQIWEKKGPLTTTEWERVRMYPDLTGRILSRVNG 361
cd00077 1 EHRFEHSLRVAQLARRLAEELGLSEEDIELLRLAALLHDIGKPGTPDAITEEESELEKDHAIVGAEILRELLLEEVIKLI 80
|
90 100 110 120 130
....*....|....*....|....*....|....*....|....*....|.
gi 111023879 362 LESVVSVAMKHRERIDGSGFPRGIAGAELTAKDRLLAAADAYQRLLEPRPH 412
cd00077 81 DELILAVDASHHERLDGLGYPDGLKGEEITLEARIVKLADRLDALRRDSRE 131
|
|
cl00076 |
140417 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
2 |
| 128698 |
smart00421 |
HTH_LUXR |
helix_turn_helix, Lux Regulon |
helix_turn_helix, Lux Regulon |
false |
false |
false |
58 |
1e-16 |
82.96 |
93.10 |
1,456,0,54 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 111023879 457 PAGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQA 510
smart00421 1 LASLTPREREVLRLLAEGLTNKEIAERLGISEKTVKTHLSNIMRKLGVRSRTQA 54
|
|
cl10457 |
142561 |
LuxR_C_like |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-helix motif and binds DNA. Proteins belonging to this group are response regulators; some act as transcriptional activators, others as transcriptional repressors. Many are active as homodimers. Many are two domain proteins in which the DNA binding property of the C-terminal DNA binding domain is modulated by modifications of the N-terminal domain. For example in the case of Lux R which participates in the regulation of gene expression in response to fluctuations in cell-population density (quorum-sensing), a signaling molecule, the pheromone Acyl HSL (N-acyl derivatives of homoserine lactone), binds to the N-terminal domain and leads to LuxR dimerization. For others phophorylation of the N-terminal domain leads to multimerization, for example Escherichia coli NarL and Sinorhizobium melilot FixJ. NarL controls gene expression of many respiratory-related operons when environmental nitrate or nitrite is present under anerobic conditions. FixJ is involved in the transcriptional activation of nitrogen fixation genes. The group also includes small proteins which lack an N-terminal signaling domain, such as Bacillus subtilis GerE. GerE is dimeric and acts in conjunction with sigmaK as an activator or a repressor modulating the expression of various genes in particular those encoding the spore-coat. These LuxR family regulators may share a similar organization of their target binding sites. For example the LuxR dimer binds the lux box, a 20bp inverted repeat, GerE dimers bind two 12bp consensus sequences in inverted orientation having the central four bases overlap, and the NarL dimer binds two 7bp inverted repeats separated by 2 bp. |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-... |
-1 |
| 109261 |
pfam00196 |
GerE |
Bacterial regulatory proteins, luxR family |
Bacterial regulatory proteins, luxR family |
false |
false |
false |
58 |
3e-14 |
75.29 |
87.93 |
1,459,3,51 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|.
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQA 510
pfam00196 4 LSPREREVLRLLAAGKSNKEIADILGISEKTVKVHRSNIMRKLNVHSRVEL 54
|
|
cl10457 |
142561 |
LuxR_C_like |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-helix motif and binds DNA. Proteins belonging to this group are response regulators; some act as transcriptional activators, others as transcriptional repressors. Many are active as homodimers. Many are two domain proteins in which the DNA binding property of the C-terminal DNA binding domain is modulated by modifications of the N-terminal domain. For example in the case of Lux R which participates in the regulation of gene expression in response to fluctuations in cell-population density (quorum-sensing), a signaling molecule, the pheromone Acyl HSL (N-acyl derivatives of homoserine lactone), binds to the N-terminal domain and leads to LuxR dimerization. For others phophorylation of the N-terminal domain leads to multimerization, for example Escherichia coli NarL and Sinorhizobium melilot FixJ. NarL controls gene expression of many respiratory-related operons when environmental nitrate or nitrite is present under anerobic conditions. FixJ is involved in the transcriptional activation of nitrogen fixation genes. The group also includes small proteins which lack an N-terminal signaling domain, such as Bacillus subtilis GerE. GerE is dimeric and acts in conjunction with sigmaK as an activator or a repressor modulating the expression of various genes in particular those encoding the spore-coat. These LuxR family regulators may share a similar organization of their target binding sites. For example the LuxR dimer binds the lux box, a 20bp inverted repeat, GerE dimers bind two 12bp consensus sequences in inverted orientation having the central four bases overlap, and the NarL dimer binds two 7bp inverted repeats separated by 2 bp. |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-... |
-1 |
| 32632 |
COG2771 |
CsgD |
DNA-binding HTH domain-containing proteins [Transcription] |
DNA-binding HTH domain-containing proteins [Transcription] |
false |
false |
false |
65 |
1e-12 |
70.01 |
98.46 |
1,456,1,64 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....
gi 111023879 457 PAGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAIDRGLV 520
COG2771 2 TADLTPREREILRLVAQGKSNKEIARILGISEETVKTHLRNIYRKLGVKNRVELVALALRLGLI 65
|
|
cl10457 |
142561 |
LuxR_C_like |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-helix motif and binds DNA. Proteins belonging to this group are response regulators; some act as transcriptional activators, others as transcriptional repressors. Many are active as homodimers. Many are two domain proteins in which the DNA binding property of the C-terminal DNA binding domain is modulated by modifications of the N-terminal domain. For example in the case of Lux R which participates in the regulation of gene expression in response to fluctuations in cell-population density (quorum-sensing), a signaling molecule, the pheromone Acyl HSL (N-acyl derivatives of homoserine lactone), binds to the N-terminal domain and leads to LuxR dimerization. For others phophorylation of the N-terminal domain leads to multimerization, for example Escherichia coli NarL and Sinorhizobium melilot FixJ. NarL controls gene expression of many respiratory-related operons when environmental nitrate or nitrite is present under anerobic conditions. FixJ is involved in the transcriptional activation of nitrogen fixation genes. The group also includes small proteins which lack an N-terminal signaling domain, such as Bacillus subtilis GerE. GerE is dimeric and acts in conjunction with sigmaK as an activator or a repressor modulating the expression of various genes in particular those encoding the spore-coat. These LuxR family regulators may share a similar organization of their target binding sites. For example the LuxR dimer binds the lux box, a 20bp inverted repeat, GerE dimers bind two 12bp consensus sequences in inverted orientation having the central four bases overlap, and the NarL dimer binds two 7bp inverted repeats separated by 2 bp. |
C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-... |
-1 |
| 110919 |
pfam01966 |
HD |
HD domain |
HD domain |
false |
false |
false |
108 |
6e-04 |
41.07 |
100.00 |
5,283,0,21,307,21,20,334,41,37,371,79,10,387,89,19 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 284 TLGHSRGVANLVAGAARHLGMspsDITHLYRAGLVHSLGKMGVSnqiwekkGPLTTTEWERVRMYPDLTGRILSRVNGLE 363
pfam01966 1 VLEHSLRVALLARELAEELGL---DPELLLLAALLHDIGKDPFG-------FLEKLEDFGIFKSHSVVGAEILRELEKRL 70
|
90 100 110 120
....*....|....*....|....*....|....*....|....
gi 111023879 364 SVVSVAMK-HRERIDGSGFprgiagAELTAKDRLLAAADAYQRL 406
pfam01966 71 GVDLELILeHHESWEGAGY------EPISLEARIVKLADRLDAL 108
|
|
cl00076 |
140417 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
-1 |
| 128747 |
smart00471 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif. |
Metal dependent phosphohydrolases with conserved 'HD' motif. |
false |
false |
false |
124 |
0.001 |
39.97 |
95.16 |
5,283,4,20,305,24,42,350,66,9,361,75,13,379,88,34 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 284 TLGHSRGVANLVAGAARHLGmsPSDITHLYRAGLVHSLGKMGVSNQIWEKKGPLTTTEWERVRMypdLTGRILSRVngLE 363
smart00471 5 VFEHSLRVAQLAAALAEELG--LLDIELLLLAALLHDIGKPGTPDSFLVKTSVLEDHHFIGAEI---LLEEEEPRI--LE 77
|
90 100 110 120 130
....*....|....*....|....*....|....*....|....*....|
gi 111023879 364 SVVSVAMKHREridgsGFPRGIAGAELTAKDRLLAAADAYQRLLEPRPHR 413
smart00471 78 EILATAILSHH-----ERPDGLRGEPITLEARIVKVADRLDALRRDRRYR 122
|
|
cl00076 |
140417 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
-1 |
| 32388 |
COG2206 |
COG2206 |
c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms] |
c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms] |
false |
true |
false |
344 |
7e-33 |
137.19 |
44.77 |
2,276,141,86,362,228,67 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 277 VDLKSPFTLGHSRGVANLVAGAARHLGMSPSDITHLYRAGLVHSLGKMGVSNQIWEKKGPLTTTEWERVRMYPDLTGRIL 356
COG2206 142 IKAKDDYTYGHSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIGKIGIPDSILNKPGKLTEEEFEIIKKHPIYGYDIL 221
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....
gi 111023879 357 SRVNGL-ESVVSVAMKHRERIDGSGFPRGIAGAELTAKDRLLAAADAYQRLLEPRPHRLALDPRGAADRLKEEA 429
COG2206 222 KDLPEFlESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDALTSDRPYKKAKSPEEALEELRKNS 295
|
|
|
|
|
|
|
-1 |
| 33243 |
COG3437 |
COG3437 |
Response regulator containing a CheY-like receiver domain and an HD-GYP domain [Transcription / Signal transduction mechanisms] |
Response regulator containing a CheY-like receiver domain and an HD-GYP domain [... |
false |
true |
false |
360 |
2e-25 |
112.31 |
48.89 |
2,256,158,105,361,264,70 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 257 RDRTLTAEESDELLGAMADFVDLKSPFTLGHSRGVANLVAGAARHLGMSPSDITHLYRAGLVHSLGKMGVSNQIWEKKGP 336
COG3437 159 EELAQIEDNLDETLEELAALLEVRDYETGDHLERVAQYSELLAELLGLSEEEVDLIKKAAPLHDIGKVAIPDSILLKPGK 238
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 337 LTTTEWERVRMYPDLTGRILSRVNG-LESVVSVAMKHRERIDGSGFPRGIAGAELTAKDRLLAAADAYQRLLEPRPHRLA 415
COG3437 239 LTSEEFEIMKGHPILGAEILKSSERlMQVAAEIARHHHERWDGSGYPDGLKGDEIPLSARIVAIADVFDALVSGRPYKEA 318
|
170
....*....|....*.
gi 111023879 416 LDPRGAADRLKEEART 431
COG3437 319 MSTEEALEIIRAQSGR 334
|
|
|
|
|
|
|
-1 |
| 32379 |
COG2197 |
CitB |
Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription] |
Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain... |
false |
true |
false |
211 |
5e-17 |
84.24 |
34.60 |
1,447,136,73 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|...
gi 111023879 448 QRVSRRTPWPAGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAIDRGLV 520
COG2197 137 PSSSAEAPLAELLTPRELEVLRLLAEGLSNKEIAEELNLSEKTVKTHVSNILRKLGVRNRTEAAIRALRLGLI 209
|
|
|
|
|
|
|
-1 |
| 32733 |
COG2909 |
MalT |
ATP-dependent transcriptional regulator [Transcription] |
ATP-dependent transcriptional regulator [Transcription] |
false |
true |
false |
894 |
1e-11 |
66.10 |
6.82 |
1,458,830,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 111023879 459 GLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAIDRGL 519
COG2909 831 PLSQRELEVLGLIAQGLSNEEIAQELFISLTTVKTHIRNIYQKLGVANRTQAVQRAKELGL 891
|
|
|
|
|
|
|
-1 |
| 132065 |
TIGR03020 |
EpsA |
transcriptional regulator EpsA |
transcriptional regulator EpsA |
false |
true |
false |
247 |
3e-10 |
62.11 |
23.89 |
2,446,182,7,458,189,52 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....
gi 111023879 447 GQRVSRRtpwpaGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQA 510
TIGR03020 183 GERHSAG-----LITAREAEILAWVRDGKTNEEIAAILGISSLTVKNHLQHIFKKLDVRNRAQA 241
|
|
|
|
|
|
|
-1 |
| 137688 |
PRK10100 |
PRK10100 |
DNA-binding transcriptional regulator CsgD; Provisional |
DNA-binding transcriptional regulator CsgD; Provisional |
false |
true |
false |
216 |
2e-09 |
59.19 |
24.54 |
1,457,153,53 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|...
gi 111023879 458 AGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQA 510
PRK10100 154 ALLTHREKEILNKLRIGASNNEIARSLFISENTVKTHLYNLFKKIAVKNRTQA 206
|
|
|
|
|
|
|
-1 |
| 138058 |
PRK10651 |
PRK10651 |
transcriptional regulator NarL; Provisional |
transcriptional regulator NarL; Provisional |
false |
true |
false |
216 |
8e-09 |
57.38 |
25.00 |
1,457,153,54 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 111023879 458 AGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQAS 511
PRK10651 154 NQLTPRERDILKLIAQGLSNKMIARRLDITESTVKVHVKHMLKKMKLKSRVEAA 207
|
|
|
|
|
|
|
-1 |
| 33243 |
COG3437 |
COG3437 |
Response regulator containing a CheY-like receiver domain and an HD-GYP domain [Transcription / Signal transduction mechanisms] |
Response regulator containing a CheY-like receiver domain and an HD-GYP domain [... |
true |
true |
false |
360 |
4e-08 |
54.92 |
24.72 |
3,158,265,10,168,276,31,199,313,41 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 159 QVGKALAYVF-ERWDGRGLPNGCRGEGIPIEIHISHVADVVE------VHLRTGGLGHAKEVLRSRRGSQFSPAVVEVFE 231
COG3437 266 QVAAEIARHHhERWDGSGYPDGLKGDEIPLSARIVAIADVFDalvsgrPYKEAMSTEEALEIIRAQSGRLFDPKLVEAFI 345
|
....*....
gi 111023879 232 RDAAAIVDG 240
COG3437 346 QVEDEIIDI 354
|
|
|
|
|
|
|
-1 |
| 32388 |
COG2206 |
COG2206 |
c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms] |
c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms] |
false |
true |
false |
344 |
1e-07 |
53.22 |
45.93 |
7,36,151,36,98,187,11,116,198,3,119,205,4,139,209,4,143,214,56,199,276,33 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 37 HMLRSSLIATRIAERMGLDPEQQATVYYANLVGWIGchadshelsalfgddiafradtyavdMTGLPFLRLMTshvgrgl 116
COG2206 152 HSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIG--------------------------KIGIPDSILNK------- 198
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 111023879 117 PGW----ERGIraavflvaargrvatlIHSH-CSSAGVLSDRMGLDGQVGKALAYVFERWDGRGLPNGCRGEGIPIEIHI 191
COG2206 199 PGKlteeEFEI----------------IKKHpIYGYDILKDLPEFLESVRAVALRHHERWDGTGYPRGLKGEEIPLEARI 262
|
170 180 190 200
....*....|....*....|....*....|....*....|....*..
gi 111023879 192 SHVADVVE------VHLRTGGLGHAKEVLRSRRGSQFSPAVVEVFER 232
COG2206 263 IAVADVYDaltsdrPYKKAKSPEEALEELRKNSGGKFDPKVVDAFLK 309
|
|
|
|
|
|
|
-1 |
| 135188 |
PRK04841 |
PRK04841 |
transcriptional regulator MalT; Provisional |
transcriptional regulator MalT; Provisional |
false |
true |
false |
903 |
3e-07 |
51.91 |
6.09 |
2,451,834,4,459,838,51 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*....
gi 111023879 452 RRTPwpagLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQA 510
PRK04841 835 RTSP----LTQREWQVLGLIYSGYSNEQIAGELDVAATTIKTHIRNLYQKLGIAHRQEA 889
|
|
|
|
|
|
|
-1 |
| 137598 |
PRK09935 |
PRK09935 |
transcriptional regulator FimZ; Provisional |
transcriptional regulator FimZ; Provisional |
false |
true |
false |
210 |
4e-07 |
51.43 |
22.38 |
1,459,149,47 |
10 20 30 40
....*....|....*....|....*....|....*....|....*..
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNN 506
PRK09935 150 LSNREVTVLRYLANGLSNKEIAEQLLLSNKTISAHKSNIYGKLGLHS 196
|
|
|
|
|
|
|
-1 |
| 137869 |
PRK10403 |
PRK10403 |
transcriptional regulator NarP; Provisional |
transcriptional regulator NarP; Provisional |
false |
true |
false |
215 |
3e-06 |
48.70 |
24.65 |
1,459,153,53 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|...
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASL 512
PRK10403 154 LTERELDVLHELAQGLSNKQIASVLNISEQTVKVHIRNLLRKLNVRSRVAATI 206
|
|
|
|
|
|
|
-1 |
| 132580 |
TIGR03541 |
reg_near_HchA |
LuxR family transcriptional regulatory, chaperone HchA-associated |
LuxR family transcriptional regulatory, chaperone HchA-associated |
false |
true |
false |
232 |
3e-06 |
48.63 |
25.43 |
1,459,171,59 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*....
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAIDRG 518
TIGR03541 172 LSEREREVLAWTALGRRQADIAAILGISERTVENHLRSARRKLGVATTAQAIAIALRKG 230
|
|
|
|
|
|
|
-1 |
| 34204 |
COG4566 |
TtrR |
Response regulator [Signal transduction mechanisms] |
Response regulator [Signal transduction mechanisms] |
false |
true |
false |
202 |
6e-06 |
47.54 |
24.26 |
1,457,140,49 |
10 20 30 40
....*....|....*....|....*....|....*....|....*....
gi 111023879 458 AGLTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNN 506
COG4566 141 ATLTPRERQVLDLVVRGLMNKQIAFDLGISERTVELHRANVMEKMQARS 189
|
|
|
|
|
|
|
-1 |
| 137737 |
PRK10188 |
PRK10188 |
DNA-binding transcriptional activator SdiA; Provisional |
DNA-binding transcriptional activator SdiA; Provisional |
false |
true |
false |
240 |
2e-04 |
42.88 |
25.42 |
1,459,179,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAIDRGLV 520
PRK10188 180 FSKREKEILKWTAEGKTSAEIAMILSISENTVNFHQKNMQKKFNAPNKTQIACYAAATGLI 240
|
|
|
|
|
|
|
-1 |
| 136118 |
PRK06930 |
PRK06930 |
positive control sigma-like factor; Validated |
positive control sigma-like factor; Validated |
false |
true |
false |
170 |
0.005 |
37.78 |
31.18 |
3,459,114,11,470,126,27,499,153,14 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 111023879 460 LTDREVEILRL-VAQGRSNREIAADLFIAEKTARNHVERvyAKLGVNNRTQASLA 513
PRK06930 115 LTEREKEVYLMhRGYGLSYSEIAAYLNIKKSTVQSMIER--AEKKIAKQINESLF 167
|
|
|
|
|
|
|
-1 |
| 137846 |
PRK10360 |
PRK10360 |
DNA-binding transcriptional activator UhpA; Provisional |
DNA-binding transcriptional activator UhpA; Provisional |
false |
true |
false |
196 |
0.006 |
37.70 |
29.08 |
1,459,137,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 111023879 460 LTDREVEILRLVAQGRSNREIAADLFIAEKTARNHVERVYAKLGVNNRTQASLAAID 516
PRK10360 138 LTKRERQVAEKLAQGMAVKEIAAELGLSPKTVHVHRANLMEKLGVSNDVELARRMFD 194
|
|
|
|
|
|
|
-1 |