| 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 |
71.41 |
100.00 |
1,457,0,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 120403052 458 LTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALN 514
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 |
8e-14 |
73.71 |
93.10 |
1,454,0,54 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 120403052 455 PGGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGA 508
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 |
4e-11 |
64.89 |
94.83 |
1,457,3,55 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 120403052 458 LTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFA 512
pfam00196 4 LSPREREVLRLLAAGKSNKEIADILGISEKTVKVHRSNIMRKLNVHSRVELIRLA 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 |
4e-11 |
65.01 |
100.00 |
1,453,0,65 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 120403052 454 RPGGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNHGLV 518
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 |
2e-04 |
42.37 |
60.69 |
3,310,31,18,335,49,25,360,81,38 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 311 RRAGHLHDLGRIGVSNQIwskpsslTARELERVRLHPYLTVRILSQVGGL-------DAVAQVAGNHHEYLDGSGYPRGL 383
cd00077 32 RLAALLHDIGKPGTPDAI-------TEEESELEKDHAIVGAEILRELLLEeviklidELILAVDASHHERLDGLGYPDGL 104
|
90
....*....|....*
gi 120403052 384 PAAALSLPDRLLAAA 398
cd00077 105 KGEEITLEARIVKLA 119
|
|
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] |
true |
true |
false |
344 |
1e-28 |
122.94 |
51.16 |
3,274,141,86,360,228,65,426,293,24 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 275 VDLKCPFTLGHSRAVAELAAGAAAVVGLDADTVTVVRRAGHLHDLGRIGVSNQIWSKPSSLTARELERVRLHPYLTVRIL 354
COG2206 142 IKAKDDYTYGHSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIGKIGIPDSILNKPGKLTEEEFEIIKKHPIYGYDIL 221
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 355 SQVGGL-DAVAQVAGNHHEYLDGSGYPRGLPAAALSLPDRLLAAAVAYQSALEPRPYRDPLPATSAAARLRErVREGRLD 433
COG2206 222 KDLPEFlESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDALTSDRPYKKAKSPEEALEELRK-NSGGKFD 300
|
170
....*....|....*..
gi 120403052 434 EVAVEAVLQAAGHRARG 450
COG2206 301 PKVVDAFLKALSKYPIG 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 |
88.82 |
36.11 |
4,312,216,45,357,262,68,427,330,5,432,336,10 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 313 AGHLHDLGRIGVSNQIWSKPSSLTARELERVRLHPYLTVRILSQV-GGLDAVAQVAGNHHEYLDGSGYPRGLPAAALSLP 391
COG3437 217 AAPLHDIGKVAIPDSILLKPGKLTSEEFEIMKGHPILGAEILKSSeRLMQVAAEIARHHHERWDGSGYPDGLKGDEIPLS 296
|
90 100 110 120 130
....*....|....*....|....*....|....*....|....*....|..
gi 120403052 392 DRLLAAAVAYQSALEPRPYRDPLPATSAAARLRErvREGRL-DEVAVEAVLQ 442
COG3437 297 ARIVAIADVFDALVSGRPYKEAMSTEEALEIIRA--QSGRLfDPKLVEAFIQ 346
|
|
|
|
|
|
|
-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 |
2e-15 |
78.84 |
39.81 |
1,436,127,84 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 437 VEAVLQAAGHRARGHSPRPGGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNHG 516
COG2197 128 IARKLAGLLPSSSAEAPLAELLTPRELEVLRLLAEGLSNKEIAEELNLSEKTVKTHVSNILRKLGVRNRTEAAIRALRLG 207
|
....
gi 120403052 517 LVAP 520
COG2197 208 LIEA 211
|
|
|
|
|
|
|
-1 |
| 132065 |
TIGR03020 |
EpsA |
transcriptional regulator EpsA |
transcriptional regulator EpsA |
false |
true |
false |
247 |
6e-08 |
54.40 |
30.77 |
2,439,165,16,455,188,53 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 120403052 440 VLQAAGHRARGHSPRP-------GGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGA 508
TIGR03020 166 ALRRVLFLPNQHRTRPlgerhsaGLITAREAEILAWVRDGKTNEEIAAILGISSLTVKNHLQHIFKKLDVRNRAQA 241
|
|
|
|
|
|
|
-1 |
| 138058 |
PRK10651 |
PRK10651 |
transcriptional regulator NarL; Provisional |
transcriptional regulator NarL; Provisional |
false |
true |
false |
216 |
5e-07 |
51.22 |
27.31 |
1,456,154,59 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*....
gi 120403052 457 GLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNH 515
PRK10651 155 QLTPRERDILKLIAQGLSNKMIARRLDITESTVKVHVKHMLKKMKLKSRVEAAVWVHQE 213
|
|
|
|
|
|
|
-1 |
| 32733 |
COG2909 |
MalT |
ATP-dependent transcriptional regulator [Transcription] |
ATP-dependent transcriptional regulator [Transcription] |
false |
true |
false |
894 |
6e-07 |
50.69 |
5.82 |
1,456,830,52 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|..
gi 120403052 457 GLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGA 508
COG2909 831 PLSQRELEVLGLIAQGLSNEEIAQELFISLTTVKTHIRNIYQKLGVANRTQA 882
|
|
|
|
|
|
|
-1 |
| 34204 |
COG4566 |
TtrR |
Response regulator [Signal transduction mechanisms] |
Response regulator [Signal transduction mechanisms] |
false |
true |
false |
202 |
2e-06 |
49.08 |
34.65 |
1,434,119,70 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 435 VAVEAVLQAAGHRARGHSPRPGGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATN 504
COG4566 120 LARDASRRAEADRQAAIRARLATLTPRERQVLDLVVRGLMNKQIAFDLGISERTVELHRANVMEKMQARS 189
|
|
|
|
|
|
|
-1 |
| 137869 |
PRK10403 |
PRK10403 |
transcriptional regulator NarP; Provisional |
transcriptional regulator NarP; Provisional |
false |
true |
false |
215 |
5e-06 |
47.93 |
46.98 |
4,417,110,13,430,124,19,449,144,6,455,151,60 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 120403052 418 SAAARLRERVREG-RLDEVAVEAVLQAAGHRAR-GHSPRP-GGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVE 494
PRK10403 111 SDPEVLLEAIRAGaKGSKVFSERVNQYLREREMfGAEEDPfSVLTERELDVLHELAQGLSNKQIASVLNISEQTVKVHIR 190
|
90 100
....*....|....*....|.
gi 120403052 495 RTYAKIGATNRIGASMFALNH 515
PRK10403 191 NLLRKLNVRSRVAATILFLQQ 211
|
|
|
|
|
|
|
-1 |
| 135188 |
PRK04841 |
PRK04841 |
transcriptional regulator MalT; Provisional |
transcriptional regulator MalT; Provisional |
false |
true |
false |
903 |
2e-05 |
46.13 |
5.65 |
2,450,835,3,457,838,48 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 120403052 451 HSPrpggLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNR 505
PRK04841 836 TSP----LTQREWQVLGLIYSGYSNEQIAGELDVAATTIKTHIRNLYQKLGIAHR 886
|
|
|
|
|
|
|
-1 |
| 137598 |
PRK09935 |
PRK09935 |
transcriptional regulator FimZ; Provisional |
transcriptional regulator FimZ; Provisional |
false |
true |
false |
210 |
3e-05 |
45.65 |
29.05 |
1,457,149,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 120403052 458 LTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNHGLV 518
PRK09935 150 LSNREVTVLRYLANGLSNKEIAEQLLLSNKTISAHKSNIYGKLGLHSIVELIDYAKSHELL 210
|
|
|
|
|
|
|
-1 |
| 137688 |
PRK10100 |
PRK10100 |
DNA-binding transcriptional regulator CsgD; Provisional |
DNA-binding transcriptional regulator CsgD; Provisional |
false |
true |
false |
216 |
5e-05 |
44.55 |
26.85 |
1,457,155,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 120403052 458 LTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNH 515
PRK10100 156 LTHREKEILNKLRIGASNNEIARSLFISENTVKTHLYNLFKKIAVKNRTQAVSWANDN 213
|
|
|
|
|
|
|
-1 |
| 132580 |
TIGR03541 |
reg_near_HchA |
LuxR family transcriptional regulatory, chaperone HchA-associated |
LuxR family transcriptional regulatory, chaperone HchA-associated |
false |
true |
false |
232 |
6e-05 |
44.39 |
27.16 |
1,453,167,63 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|...
gi 120403052 454 RPGGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNHG 516
TIGR03541 168 EAGVLSEREREVLAWTALGRRQADIAAILGISERTVENHLRSARRKLGVATTAQAIAIALRKG 230
|
|
|
|
|
|
|
-1 |
| 139792 |
PRK13719 |
PRK13719 |
conjugal transfer transcriptional regulator TraJ; Provisional |
conjugal transfer transcriptional regulator TraJ; Provisional |
false |
true |
false |
220 |
3e-04 |
42.05 |
26.82 |
1,461,149,59 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*....
gi 120403052 462 EIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRIGASMFALNHGLVAP 520
PRK13719 150 QYDVFILYSFGFSHNSIASLLNITNGSSKNKISEILKFFGISSRDELLIILHTSEMISP 208
|
|
|
|
|
|
|
-1 |
| 136118 |
PRK06930 |
PRK06930 |
positive control sigma-like factor; Validated |
positive control sigma-like factor; Validated |
false |
true |
false |
170 |
0.002 |
39.32 |
32.35 |
3,457,114,11,468,126,33,503,159,10 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 120403052 458 LTPREIEVLCL-VARGASNKEIAATLGISGKTARNHVERTYAKIGatNRIGASMFAL 513
PRK06930 115 LTEREKEVYLMhRGYGLSYSEIAAYLNIKKSTVQSMIERAEKKIA--KQINESLFCM 169
|
|
|
|
|
|
|
-1 |
| 137244 |
PRK09390 |
fixJ |
response regulator FixJ; Provisional |
response regulator FixJ; Provisional |
false |
true |
false |
202 |
0.005 |
38.08 |
37.13 |
2,435,113,17,452,136,52 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 120403052 436 AVEAVLQAAGHRARGHS------PRPGGLTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATN 504
PRK09390 114 AIERALAQAPAAAKSEAvaadirARIASLSERERQVMDGLVAGLSNKVIARDLDISPRTVEVYRANVMTKMQAGS 188
|
|
|
|
|
|
|
-1 |
| 132030 |
TIGR02985 |
Sig70_bacteroi1 |
RNA polymerase sigma-70 factor, Bacteroides expansion family 1 |
RNA polymerase sigma-70 factor, Bacteroides expansion family 1 |
false |
true |
false |
161 |
0.006 |
37.56 |
24.22 |
2,460,118,9,470,127,30 |
10 20 30 40
....*....|....*....|....*....|....*....|
gi 120403052 461 REIEVLCLVaRGASNKEIAATLGISGKTARNHVERTYAKI 500
TIGR02985 119 RKIFILSRF-EGKSYKEIAEELGISVKTVEYHISKALKEL 157
|
|
|
|
|
|
|
-1 |
| 137846 |
PRK10360 |
PRK10360 |
DNA-binding transcriptional activator UhpA; Provisional |
DNA-binding transcriptional activator UhpA; Provisional |
false |
true |
false |
196 |
0.008 |
37.31 |
25.00 |
1,457,137,49 |
10 20 30 40
....*....|....*....|....*....|....*....|....*....
gi 120403052 458 LTPREIEVLCLVARGASNKEIAATLGISGKTARNHVERTYAKIGATNRI 506
PRK10360 138 LTKRERQVAEKLAQGMAVKEIAAELGLSPKTVHVHRANLMEKLGVSNDV 186
|
|
|
|
|
|
|
-1 |