| 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 |
6e-13 |
71.03 |
100.00 |
1,455,0,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 41409450 456 LTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQ 512
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 |
| 128698 |
smart00421 |
HTH_LUXR |
helix_turn_helix, Lux Regulon |
helix_turn_helix, Lux Regulon |
false |
false |
false |
58 |
4e-14 |
74.87 |
100.00 |
1,452,0,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 41409450 453 PDGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYA 510
smart00421 1 LASLTPREREVLRLLAEGLTNKEIAERLGISEKTVKTHLSNIMRKLGVRSRTQAVRLA 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 |
4e-12 |
67.98 |
98.28 |
1,453,1,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 41409450 454 DGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYA 510
pfam00196 2 DSLSPREREVLRLLAAGKSNKEIADILGISEKTVKVHRSNIMRKLNVHSRVELIRLA 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 |
7e-11 |
63.85 |
100.00 |
1,451,0,65 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 41409450 452 RPDGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQHGLV 516
COG2771 1 RTADLTPREREILRLVAQGKSNKEIARILGISEETVKTHLRNIYRKLGVKNRVELVALALRLGLI 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 |
43.14 |
78.62 |
4,305,29,23,335,52,27,362,86,33,395,120,23 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 306 LTRRAGHVHDLGRIGVSNQIWSRpgplsgsQFERVRLHPYLTVRILDQVPGLRRLAE-------VAGNHHECLDGSGYPR 378
cd00077 30 LLRLAALLHDIGKPGTPDAITEE-------ESELEKDHAIVGAEILRELLLEEVIKLidelilaVDASHHERLDGLGYPD 102
|
90 100 110 120
....*....|....*....|....*....|....*....|.
gi 41409450 379 GLAGPALGMPDRILAAA-VCYQSGREPRPYREQLSEAEAAR 418
cd00077 103 GLKGEEITLEARIVKLAdRLDALRRDSREKRRRIAEEDLEE 143
|
|
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 |
1e-27 |
119.86 |
56.10 |
5,255,124,16,271,141,86,357,228,64,422,292,14,436,307,10 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 256 VDEQSLDAALVALGDF-VDLKCPFTLGHSRAVARLAGQAARAAGLDADAVALTRRAGHVHDLGRIGVSNQIWSRPGPLSG 334
COG2206 125 VAREIVKKALVALARGdIKAKDDYTYGHSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIGKIGIPDSILNKPGKLTE 204
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 335 SQFERVRLHPYLTVRILDQVPGL-RRLAEVAGNHHECLDGSGYPRGLAGPALGMPDRILAAAVCYQSGREPRPYREQLSE 413
COG2206 205 EEFEIIKKHPIYGYDILKDLPEFlESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDALTSDRPYKKAKSP 284
|
170 180 190
....*....|....*....|....*....|....
gi 41409450 414 AEAARRLRgRVRCGELDPVAAEA-VLHAAGQPVG 446
COG2206 285 EEALEELR-KNSGGKFDPKVVDAfLKALSKYPIG 317
|
|
|
|
|
|
|
-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-18 |
89.20 |
46.11 |
2,257,164,104,361,269,61 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 258 EQSLDAALVALGDFVDLKCPFTLGHSRAVARLAGQAARAAGLDADAVALTRRAGHVHDLGRIGVSNQIWSRPGPLSGSQF 337
COG3437 165 EDNLDETLEELAALLEVRDYETGDHLERVAQYSELLAELLGLSEEEVDLIKKAAPLHDIGKVAIPDSILLKPGKLTSEEF 244
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 338 ERVRLHPYLTVRILDQVPGLRRLA-EVAGNHHECLDGSGYPRGLAGPALGMPDRILAAAVCYQSGREPRPYREQLSEAEA 416
COG3437 245 EIMKGHPILGAEILKSSERLMQVAaEIARHHHERWDGSGYPDGLKGDEIPLSARIVAIADVFDALVSGRPYKEAMSTEEA 324
|
....*.
gi 41409450 417 ARRLRG 422
COG3437 325 LEIIRA 330
|
|
|
|
|
|
|
-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 |
6e-17 |
84.24 |
41.23 |
2,427,122,17,446,139,70 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 428 ELDPVAAEAVLHAAGQPvgPRPNPRPDGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGAS 507
COG2197 123 YLPPDIARKLAGLLPSS--SAEAPLAELLTPRELEVLRLLAEGLSNKEIAEELNLSEKTVKTHVSNILRKLGVRNRTEAA 200
|
....*....
gi 41409450 508 MYALQHGLV 516
COG2197 201 IRALRLGLI 209
|
|
|
|
|
|
|
-1 |
| 32733 |
COG2909 |
MalT |
ATP-dependent transcriptional regulator [Transcription] |
ATP-dependent transcriptional regulator [Transcription] |
false |
true |
false |
894 |
5e-09 |
58.01 |
11.63 |
2,398,787,40,451,827,64 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 399 QSGREPRPYREQLSEAEAARRLRGRVRCGELDPVAAEAVLhaagqpvgprpnpRPDGLTPREIEVLGHVARGASNKEIAA 478
COG2909 788 LLGELPELERHRLQRILREILQTQRQKFIHLDEEFVEGLL-------------NELPLSQRELEVLGLIAQGLSNEEIAQ 854
|
90 100 110
....*....|....*....|....*....|....*..
gi 41409450 479 ALVISEKTARNHVERTYAKIGVSNRIGASMYALQHGL 515
COG2909 855 ELFISLTTVKTHIRNIYQKLGVANRTQAVQRAKELGL 891
|
|
|
|
|
|
|
-1 |
| 137869 |
PRK10403 |
PRK10403 |
transcriptional regulator NarP; Provisional |
transcriptional regulator NarP; Provisional |
false |
true |
false |
215 |
8e-09 |
57.18 |
32.56 |
2,442,141,12,455,153,58 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|.
gi 41409450 443 QPVGPRPNPRPDgLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQH 513
PRK10403 142 EMFGAEEDPFSV-LTERELDVLHELAQGLSNKQIASVLNISEQTVKVHIRNLLRKLNVRSRVAATILFLQQ 211
|
|
|
|
|
|
|
-1 |
| 138058 |
PRK10651 |
PRK10651 |
transcriptional regulator NarL; Provisional |
transcriptional regulator NarL; Provisional |
false |
true |
false |
216 |
1e-08 |
56.61 |
32.87 |
2,447,142,6,453,153,60 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|.
gi 41409450 448 RPNPRP-----DGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQH 513
PRK10651 143 RANRATterdvNQLTPRERDILKLIAQGLSNKMIARRLDITESTVKVHVKHMLKKMKLKSRVEAAVWVHQE 213
|
|
|
|
|
|
|
-1 |
| 132065 |
TIGR03020 |
EpsA |
transcriptional regulator EpsA |
transcriptional regulator EpsA |
false |
true |
false |
247 |
1e-08 |
56.33 |
29.96 |
2,436,173,16,454,189,58 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 41409450 437 VLHAAGQPVGPRPNPRpdGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQ 512
TIGR03020 174 PNQHRTRPLGERHSAG--LITAREAEILAWVRDGKTNEEIAAILGISSLTVKNHLQHIFKKLDVRNRAQAVAKAIA 247
|
|
|
|
|
|
|
-1 |
| 137688 |
PRK10100 |
PRK10100 |
DNA-binding transcriptional regulator CsgD; Provisional |
DNA-binding transcriptional regulator CsgD; Provisional |
false |
true |
false |
216 |
4e-08 |
54.57 |
26.85 |
1,455,155,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 41409450 456 LTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQH 513
PRK10100 156 LTHREKEILNKLRIGASNNEIARSLFISENTVKTHLYNLFKKIAVKNRTQAVSWANDN 213
|
|
|
|
|
|
|
-1 |
| 137598 |
PRK09935 |
PRK09935 |
transcriptional regulator FimZ; Provisional |
transcriptional regulator FimZ; Provisional |
false |
true |
false |
210 |
4e-07 |
51.43 |
29.05 |
1,455,149,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 41409450 456 LTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQHGLV 516
PRK09935 150 LSNREVTVLRYLANGLSNKEIAEQLLLSNKTISAHKSNIYGKLGLHSIVELIDYAKSHELL 210
|
|
|
|
|
|
|
-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 |
3e-06 |
48.60 |
29.65 |
4,133,207,6,139,214,56,195,272,6,201,282,27 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 41409450 134 RLIHSH-CASAALLADRIGLGPNVQAALAYTFERYDGGGLPTGARGEDIPIQMRIAQLADMVE--VHHRSY----GVAGA 206
COG2206 208 EIIKKHpIYGYDILKDLPEFLESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDalTSDRPYkkakSPEEA 287
|
90 100
....*....|....*....|..
gi 41409450 207 VAMVGARRGGQFDPGIADVFLR 228
COG2206 288 LEELRKNSGGKFDPKVVDAFLK 309
|
|
|
|
|
|
|
-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 |
6e-06 |
47.60 |
21.67 |
3,164,276,31,195,309,22,217,335,19 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 41409450 165 ERYDGGGLPTGARGEDIPIQMRIAQLADMVE--VHHRSYGVAGAVAMVGARRGGQ----FDPGIADVFLRDADAILAG 236
COG3437 277 ERWDGSGYPDGLKGDEIPLSARIVAIADVFDalVSGRPYKEAMSTEEALEIIRAQsgrlFDPKLVEAFIQVEDEIIDI 354
|
|
|
|
|
|
|
-1 |
| 34204 |
COG4566 |
TtrR |
Response regulator [Signal transduction mechanisms] |
Response regulator [Signal transduction mechanisms] |
false |
true |
false |
202 |
2e-05 |
46.00 |
25.25 |
1,451,138,51 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|.
gi 41409450 452 RPDGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSN 502
COG4566 139 RLATLTPRERQVLDLVVRGLMNKQIAFDLGISERTVELHRANVMEKMQARS 189
|
|
|
|
|
|
|
-1 |
| 135188 |
PRK04841 |
PRK04841 |
transcriptional regulator MalT; Provisional |
transcriptional regulator MalT; Provisional |
false |
true |
false |
903 |
2e-05 |
45.75 |
6.09 |
1,455,838,55 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 41409450 456 LTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYA 510
PRK04841 839 LTQREWQVLGLIYSGYSNEQIAGELDVAATTIKTHIRNLYQKLGIAHRQEAVQLA 893
|
|
|
|
|
|
|
-1 |
| 132580 |
TIGR03541 |
reg_near_HchA |
LuxR family transcriptional regulatory, chaperone HchA-associated |
LuxR family transcriptional regulatory, chaperone HchA-associated |
false |
true |
false |
232 |
2e-04 |
42.85 |
25.43 |
1,455,171,59 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*....
gi 41409450 456 LTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQHG 514
TIGR03541 172 LSEREREVLAWTALGRRQADIAAILGISERTVENHLRSARRKLGVATTAQAIAIALRKG 230
|
|
|
|
|
|
|
-1 |
| 139792 |
PRK13719 |
PRK13719 |
conjugal transfer transcriptional regulator TraJ; Provisional |
conjugal transfer transcriptional regulator TraJ; Provisional |
false |
true |
false |
220 |
7e-04 |
40.89 |
20.00 |
1,459,149,44 |
10 20 30 40
....*....|....*....|....*....|....*....|....
gi 41409450 460 EIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNR 503
PRK13719 150 QYDVFILYSFGFSHNSIASLLNITNGSSKNKISEILKFFGISSR 193
|
|
|
|
|
|
|
-1 |
| 137846 |
PRK10360 |
PRK10360 |
DNA-binding transcriptional activator UhpA; Provisional |
DNA-binding transcriptional activator UhpA; Provisional |
false |
true |
false |
196 |
0.002 |
39.24 |
27.04 |
1,451,133,53 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|...
gi 41409450 452 RPDGLTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRI 504
PRK10360 134 RQDPLTKRERQVAEKLAQGMAVKEIAAELGLSPKTVHVHRANLMEKLGVSNDV 186
|
|
|
|
|
|
|
-1 |
| 136118 |
PRK06930 |
PRK06930 |
positive control sigma-like factor; Validated |
positive control sigma-like factor; Validated |
false |
true |
false |
170 |
0.004 |
38.16 |
32.35 |
3,455,114,8,463,123,36,501,159,10 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 41409450 456 LTPREIEV-LGHVARGASNKEIAAALVISEKTARNHVERTYAKIGvsNRIGASMYAL 511
PRK06930 115 LTEREKEVyLMHRGYGLSYSEIAAYLNIKKSTVQSMIERAEKKIA--KQINESLFCM 169
|
|
|
|
|
|
|
-1 |
| 137737 |
PRK10188 |
PRK10188 |
DNA-binding transcriptional activator SdiA; Provisional |
DNA-binding transcriptional activator SdiA; Provisional |
false |
true |
false |
240 |
0.007 |
37.49 |
25.42 |
1,455,179,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 41409450 456 LTPREIEVLGHVARGASNKEIAAALVISEKTARNHVERTYAKIGVSNRIGASMYALQHGLV 516
PRK10188 180 FSKREKEILKWTAEGKTSAEIAMILSISENTVNFHQKNMQKKFNAPNKTQIACYAAATGLI 240
|
|
|
|
|
|
|
-1 |