| 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 |
5e-13 |
71.03 |
98.25 |
1,462,1,56 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*.
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALE 518
cd06170 2 TPREREVLRLLAEGKTNKEIADILGISEKTVKTHLRNIMRKLGVKSRTQLVAYAIR 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 |
| 128698 |
smart00421 |
HTH_LUXR |
helix_turn_helix, Lux Regulon |
helix_turn_helix, Lux Regulon |
false |
false |
false |
58 |
1e-13 |
73.33 |
93.10 |
1,462,4,54 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYA 516
smart00421 5 TPREREVLRLLAEGLTNKEIAERLGISEKTVKTHLSNIMRKLGVRSRTQAVRLA 58
|
|
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 |
7e-12 |
67.20 |
93.10 |
1,462,4,54 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYA 516
pfam00196 5 SPREREVLRLLAAGKSNKEIADILGISEKTVKVHRSNIMRKLNVHSRVELIRLA 58
|
|
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 |
6e-11 |
64.24 |
92.31 |
1,462,5,60 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEHGLL 522
COG2771 6 TPREREILRLVAQGKSNKEIARILGISEETVKTHLRNIYRKLGVKNRVELVALALRLGLI 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 |
| 28958 |
cd00077 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
true |
false |
true |
145 |
1e-04 |
43.53 |
60.00 |
3,313,29,23,343,52,24,367,83,33 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 314 LTRRAGHVHDIGRIGVSNQVWSKgsalstaEFERVRLHPYLTERILRQVPGLAQ-------VAAVASNHHERLDGTGYPR 386
cd00077 30 LLRLAALLHDIGKPGTPDAITEE-------ESELEKDHAIVGAEILRELLLEEViklidelILAVDASHHERLDGLGYPD 102
|
90
....*....|....
gi 119866977 387 GLSARELTMPDRVL 400
cd00077 103 GLKGEEITLEARIV 116
|
|
cl00076 |
140417 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
2 |
| 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 |
8e-24 |
106.76 |
41.28 |
2,279,141,86,365,228,55 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 280 VDLKCPFTAGHSRAVAALAADAATALGLDGEAVALTRRAGHVHDIGRIGVSNQVWSKGSALSTAEFERVRLHPYLTERIL 359
COG2206 142 IKAKDDYTYGHSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIGKIGIPDSILNKPGKLTEEEFEIIKKHPIYGYDIL 221
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|..
gi 119866977 360 RQVPGL-AQVAAVASNHHERLDGTGYPRGLSARELTMPDRVLAAAVAFQAACEPRPYRAQMT 420
COG2206 222 KDLPEFlESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDALTSDRPYKKAKS 283
|
|
|
|
|
|
|
-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-16 |
82.27 |
43.33 |
2,265,164,105,370,270,50 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 266 ASGLDALLIALGDFVDLKCPFTAGHSRAVAALAADAATALGLDGEAVALTRRAGHVHDIGRIGVSNQVWSKGSALSTAEF 345
COG3437 165 EDNLDETLEELAALLEVRDYETGDHLERVAQYSELLAELLGLSEEEVDLIKKAAPLHDIGKVAIPDSILLKPGKLTSEEF 244
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 119866977 346 ERVRLHPYLTERILRQVPGLAQVAA-VASNHHERLDGTGYPRGLSARELTMPDRVLAAAVAFQAACEPRPYRAQMT 420
COG3437 245 EIMKGHPILGAEILKSSERLMQVAAeIARHHHERWDGSGYPDGLKGDEIPLSARIVAIADVFDALVSGRPYKEAMS 320
|
|
|
|
|
|
|
-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 |
3e-14 |
75.38 |
28.44 |
1,462,149,60 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEHGLL 522
COG2197 150 TPRELEVLRLLAEGLSNKEIAEELNLSEKTVKTHVSNILRKLGVRNRTEAAIRALRLGLI 209
|
|
|
|
|
|
|
-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] |
true |
true |
false |
344 |
8e-10 |
60.54 |
29.36 |
3,142,207,6,148,214,56,204,276,32 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 143 RLIHSH-CASAAMLAERIGLDDDVRRALGFTFERFDGGGLPEGASGDAIPIEMRVAQFADLLE------VHHRGYGVEGA 215
COG2206 208 EIIKKHpIYGYDILKDLPEFLESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDaltsdrPYKKAKSPEEA 287
|
90 100
....*....|....*....|.
gi 119866977 216 VAMARNRRGGQFDPAVVDAFV 236
COG2206 288 LEELRKNSGGKFDPKVVDAFL 308
|
|
|
|
|
|
|
-1 |
| 32733 |
COG2909 |
MalT |
ATP-dependent transcriptional regulator [Transcription] |
ATP-dependent transcriptional regulator [Transcription] |
false |
true |
false |
894 |
2e-09 |
58.78 |
6.94 |
1,462,832,62 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|..
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEHGLLGR 524
COG2909 833 SQRELEVLGLIAQGLSNEEIAQELFISLTTVKTHIRNIYQKLGVANRTQAVQRAKELGLLMG 894
|
|
|
|
|
|
|
-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-08 |
56.07 |
50.83 |
7,22,169,41,69,210,6,97,216,25,122,242,24,154,266,10,173,276,31,204,313,39 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 23 EVLAALSVAIDLGLGQPAEHMLRSALIATRLADRLGLTRAQrdcvyyATLIMWigchadsheyarwfgddiavrrASYLV 102
COG3437 170 ETLEELAALLEVRDYETGDHLERVAQYSELLAELLGLSEEE------VDLIKK----------------------AAPLH 221
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119866977 103 DWSGLPYQRFLLANIAHGEP-LLQRLRTATALYADARGNISRLIHshcasaamLAERIGLDDDvrralgftfERFDGGGL 181
COG3437 222 DIGKVAIPDSILLKPGKLTSeEFEIMKGHPILGAEILKSSERLMQ--------VAAEIARHHH---------ERWDGSGY 284
|
170 180 190 200 210 220
....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 119866977 182 PEGASGDAIPIEMRVAQFADLLE------VHHRGYGVEGAVAMARNRRGGQFDPAVVDAFVTDPDALL 243
COG3437 285 PDGLKGDEIPLSARIVAIADVFDalvsgrPYKEAMSTEEALEIIRAQSGRLFDPKLVEAFIQVEDEII 352
|
|
|
|
|
|
|
-1 |
| 138058 |
PRK10651 |
PRK10651 |
transcriptional regulator NarL; Provisional |
transcriptional regulator NarL; Provisional |
false |
true |
false |
216 |
2e-07 |
52.37 |
26.39 |
1,462,156,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEH 519
PRK10651 157 TPRERDILKLIAQGLSNKMIARRLDITESTVKVHVKHMLKKMKLKSRVEAAVWVHQE 213
|
|
|
|
|
|
|
-1 |
| 137869 |
PRK10403 |
PRK10403 |
transcriptional regulator NarP; Provisional |
transcriptional regulator NarP; Provisional |
false |
true |
false |
215 |
4e-07 |
51.40 |
26.51 |
1,462,154,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEH 519
PRK10403 155 TERELDVLHELAQGLSNKQIASVLNISEQTVKVHIRNLLRKLNVRSRVAATILFLQQ 211
|
|
|
|
|
|
|
-1 |
| 137688 |
PRK10100 |
PRK10100 |
DNA-binding transcriptional regulator CsgD; Provisional |
DNA-binding transcriptional regulator CsgD; Provisional |
false |
true |
false |
216 |
5e-07 |
51.10 |
26.39 |
1,462,156,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEH 519
PRK10100 157 THREKEILNKLRIGASNNEIARSLFISENTVKTHLYNLFKKIAVKNRTQAVSWANDN 213
|
|
|
|
|
|
|
-1 |
| 132065 |
TIGR03020 |
EpsA |
transcriptional regulator EpsA |
transcriptional regulator EpsA |
false |
true |
false |
247 |
9e-07 |
50.55 |
20.24 |
1,462,191,50 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAA 512
TIGR03020 192 TAREAEILAWVRDGKTNEEIAAILGISSLTVKNHLQHIFKKLDVRNRAQA 241
|
|
|
|
|
|
|
-1 |
| 137598 |
PRK09935 |
PRK09935 |
transcriptional regulator FimZ; Provisional |
transcriptional regulator FimZ; Provisional |
false |
true |
false |
210 |
2e-06 |
49.12 |
27.62 |
1,464,152,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 119866977 465 REAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEHGLL 522
PRK09935 153 REVTVLRYLANGLSNKEIAEQLLLSNKTISAHKSNIYGKLGLHSIVELIDYAKSHELL 210
|
|
|
|
|
|
|
-1 |
| 135188 |
PRK04841 |
PRK04841 |
transcriptional regulator MalT; Provisional |
transcriptional regulator MalT; Provisional |
false |
true |
false |
903 |
7e-05 |
44.20 |
5.98 |
1,462,839,54 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYA 516
PRK04841 840 TQREWQVLGLIYSGYSNEQIAGELDVAATTIKTHIRNLYQKLGIAHRQEAVQLA 893
|
|
|
|
|
|
|
-1 |
| 34204 |
COG4566 |
TtrR |
Response regulator [Signal transduction mechanisms] |
Response regulator [Signal transduction mechanisms] |
false |
true |
false |
202 |
6e-04 |
40.99 |
22.77 |
1,462,143,46 |
10 20 30 40
....*....|....*....|....*....|....*....|....*.
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSN 508
COG4566 144 TPRERQVLDLVVRGLMNKQIAFDLGISERTVELHRANVMEKMQARS 189
|
|
|
|
|
|
|
-1 |
| 132580 |
TIGR03541 |
reg_near_HchA |
LuxR family transcriptional regulatory, chaperone HchA-associated |
LuxR family transcriptional regulatory, chaperone HchA-associated |
false |
true |
false |
232 |
0.001 |
40.15 |
25.00 |
1,462,172,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEHG 520
TIGR03541 173 SEREREVLAWTALGRRQADIAAILGISERTVENHLRSARRKLGVATTAQAIAIALRKG 230
|
|
|
|
|
|
|
-1 |
| 137737 |
PRK10188 |
PRK10188 |
DNA-binding transcriptional activator SdiA; Provisional |
DNA-binding transcriptional activator SdiA; Provisional |
false |
true |
false |
240 |
0.002 |
39.41 |
24.17 |
1,464,182,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 119866977 465 REAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRVAASLYALEHGLL 522
PRK10188 183 REKEILKWTAEGKTSAEIAMILSISENTVNFHQKNMQKKFNAPNKTQIACYAAATGLI 240
|
|
|
|
|
|
|
-1 |
| 137846 |
PRK10360 |
PRK10360 |
DNA-binding transcriptional activator UhpA; Provisional |
DNA-binding transcriptional activator UhpA; Provisional |
false |
true |
false |
196 |
0.005 |
38.08 |
24.49 |
1,462,138,48 |
10 20 30 40
....*....|....*....|....*....|....*....|....*...
gi 119866977 463 TAREAEVLCLVAQGATNKEIAARLVISEKTARNHVERTYAKIGVSNRV 510
PRK10360 139 TKRERQVAEKLAQGMAVKEIAAELGLSPKTVHVHRANLMEKLGVSNDV 186
|
|
|
|
|
|
|
-1 |
| 136118 |
PRK06930 |
PRK06930 |
positive control sigma-like factor; Validated |
positive control sigma-like factor; Validated |
false |
true |
false |
170 |
0.009 |
37.01 |
31.76 |
3,462,115,10,472,126,33,507,159,10 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*.
gi 119866977 463 TAREAEVLCL-VAQGATNKEIAARLVISEKTARNHVERTYAKIGvsNRVAASLYAL 517
PRK06930 116 TEREKEVYLMhRGYGLSYSEIAAYLNIKKSTVQSMIERAEKKIA--KQINESLFCM 169
|
|
|
|
|
|
|
-1 |