| 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 |
1e-12 |
70.26 |
100.00 |
1,453,0,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119714219 454 LSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAME 510
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 |
8e-11 |
63.56 |
87.59 |
1,275,1,127 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 276 YTLGHSSGTSELAELAGRAIGLDDPAVGNLRRAALLHDLGRVGVSSGIWDKPGALTRSELEQVRLHPYHTERILACSPVL 355
cd00077 2 HRFEHSLRVAQLARRLAEELGLSEEDIELLRLAALLHDIGKPGTPDAITEEESELEKDHAIVGAEILRELLLEEVIKLID 81
|
90 100 110 120
....*....|....*....|....*....|....*....|....*..
gi 119714219 356 APLGRIAGLHHERLDGSGYHHGLAAAAIPIEARVLAAADTFQTLTQD 402
cd00077 82 ELILAVDASHHERLDGLGYPDGLKGEEITLEARIVKLADRLDALRRD 128
|
|
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-13 |
73.33 |
100.00 |
1,450,0,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 119714219 451 PSGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYA 508
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 |
2e-10 |
62.58 |
94.83 |
1,453,3,55 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 119714219 454 LSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYA 508
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 |
8e-10 |
60.38 |
98.46 |
1,450,1,64 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....
gi 119714219 451 PSGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAMEHDLL 514
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 |
| 128747 |
smart00471 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif. |
Metal dependent phosphohydrolases with conserved 'HD' motif. |
false |
false |
false |
124 |
1e-06 |
49.98 |
92.74 |
5,275,3,27,304,30,26,338,56,16,354,76,22,382,98,20 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 276 YTLGHSSGTSELAELAGRAIGLDDPAVgnLRRAALLHDLGRVGVSSGIWDKPGALtrseleqvRLHPYHTERILACSPV- 354
smart00471 4 HVFEHSLRVAQLAAALAEELGLLDIEL--LLLAALLHDIGKPGTPDSFLVKTSVL--------EDHHFIGAEILLEEEEp 73
|
90 100 110 120 130
....*....|....*....|....*....|....*....|....*....|.
gi 119714219 355 ---LAPLGRIAGLHHERLDGSGYHHglaaaaIPIEARVLAAADTFQTLTQD 402
smart00471 74 rilEEILATAILSHHERPDGLRGEP------ITLEARIVKVADRLDALRRD 118
|
|
cl00076 |
140417 |
HDc |
Metal dependent phosphohydrolases with conserved 'HD' motif |
Metal dependent phosphohydrolases with conserved 'HD' motif |
-1 |
| 110919 |
pfam01966 |
HD |
HD domain |
HD domain |
false |
false |
false |
108 |
6e-06 |
47.62 |
100.00 |
5,276,0,22,301,22,18,326,40,33,359,74,15,380,89,19 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 277 TLGHSSGTSELAELAGRAIGLDdpaVGNLRRAALLHDLGRVGVssgiwdkPGALTRSELEQVRLHPYHTERILACSPVLA 356
pfam01966 1 VLEHSLRVALLARELAEELGLD---PELLLLAALLHDIGKDPF-------GFLEKLEDFGIFKSHSVVGAEILRELEKRL 70
|
90 100 110 120
....*....|....*....|....*....|....*....|....
gi 119714219 357 PLG-RIAGLHHERLDGSGYhhglaaAAIPIEARVLAAADTFQTL 399
pfam01966 71 GVDlELILEHHESWEGAGY------EPISLEARIVKLADRLDAL 108
|
|
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 |
2e-34 |
141.81 |
50.87 |
3,268,140,81,349,222,53,403,275,40 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 269 MVDLKSTYTLGHSSGTSELAELAGRAIGLDDPAVGNLRRAALLHDLGRVGVSSGIWDKPGALTRSELEQVRLHPYHTERI 348
COG2206 141 DIKAKDDYTYGHSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIGKIGIPDSILNKPGKLTEEEFEIIKKHPIYGYDI 220
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 349 L-ACSPVLAPLGRIAGLHHERLDGSGYHHGLAAAAIPIEARVLAAADTFQTLTQDrPHRAAHPPERAAERLAEEARAGRF 427
COG2206 221 LkDLPEFLESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDALTSD-RPYKKAKSPEEALEELRKNSGGKF 299
|
170
....*....|....*.
gi 119714219 428 DTDSVRAVVEAAGEQP 443
COG2206 300 DPKVVDAFLKALSKYP 315
|
|
|
|
|
|
|
-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 |
7e-24 |
106.92 |
46.39 |
4,240,143,13,254,156,12,266,175,86,352,262,48 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 241 QEVLEVEPAPVRRiRSGELDRVARCF-------ADMVDLKSTYTLGHSSGTSELAELAGRAIGLDDPAVGNLRRAALLHD 313
COG3437 144 DQNLYLELQELRR-RTEELAQIEDNLdetleelAALLEVRDYETGDHLERVAQYSELLAELLGLSEEEVDLIKKAAPLHD 222
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 314 LGRVGVSSGIWDKPGALTRSELEQVRLHPYHTERILACS-PVLAPLGRIAGLHHERLDGSGYHHGLAAAAIPIEARVLAA 392
COG3437 223 IGKVAIPDSILLKPGKLTSEEFEIMKGHPILGAEILKSSeRLMQVAAEIARHHHERWDGSGYPDGLKGDEIPLSARIVAI 302
|
....*...
gi 119714219 393 ADTFQTLT 400
COG3437 303 ADVFDALV 310
|
|
|
|
|
|
|
-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-13 |
72.29 |
41.71 |
2,426,123,22,450,145,66 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 427 FDTDSVRAVVEAAGEQPAPVRGnwPSGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAAL 506
COG2197 124 LPPDIARKLAGLLPSSSAEAPL--AELLTPRELEVLRLLAEGLSNKEIAEELNLSEKTVKTHVSNILRKLGVRNRTEAAI 201
|
90
....*....|
gi 119714219 507 YAMEHDLLRP 516
COG2197 202 RALRLGLIEA 211
|
|
|
|
|
|
|
-1 |
| 137598 |
PRK09935 |
PRK09935 |
transcriptional regulator FimZ; Provisional |
transcriptional regulator FimZ; Provisional |
false |
true |
false |
210 |
4e-10 |
61.45 |
29.05 |
1,453,149,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 119714219 454 LSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAMEHDLL 514
PRK09935 150 LSNREVTVLRYLANGLSNKEIAEQLLLSNKTISAHKSNIYGKLGLHSIVELIDYAKSHELL 210
|
|
|
|
|
|
|
-1 |
| 32733 |
COG2909 |
MalT |
ATP-dependent transcriptional regulator [Transcription] |
ATP-dependent transcriptional regulator [Transcription] |
false |
true |
false |
894 |
2e-08 |
56.08 |
7.05 |
1,452,830,63 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|...
gi 119714219 453 GLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAMEHDLLR 515
COG2909 831 PLSQRELEVLGLIAQGLSNEEIAQELFISLTTVKTHIRNIYQKLGVANRTQAVQRAKELGLLM 893
|
|
|
|
|
|
|
-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 |
2e-08 |
55.69 |
22.78 |
3,156,271,33,189,309,9,198,319,34 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 157 IAQQFERWDGTGGPGGLAGVEITLAARVSEVAT-----QALLVHQEA-GVDAVMSMLRDRSGSWFDPSVVEACARHGADL 230
COG3437 272 ARHHHERWDGSGYPDGLKGDEIPLSARIVAIADvfdalVSGRPYKEAmSTEEALEIIRAQSGRLFDPKLVEAFIQVEDEI 351
|
..
gi 119714219 231 LR 232
COG3437 352 ID 353
|
|
|
|
|
|
|
-1 |
| 132065 |
TIGR03020 |
EpsA |
transcriptional regulator EpsA |
transcriptional regulator EpsA |
false |
true |
false |
247 |
6e-08 |
54.40 |
23.08 |
1,452,189,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119714219 453 GLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAM 509
TIGR03020 190 LITAREAEILAWVRDGKTNEEIAAILGISSLTVKNHLQHIFKKLDVRNRAQAVAKAI 246
|
|
|
|
|
|
|
-1 |
| 138058 |
PRK10651 |
PRK10651 |
transcriptional regulator NarL; Provisional |
transcriptional regulator NarL; Provisional |
false |
true |
false |
216 |
9e-08 |
53.53 |
28.70 |
1,451,153,62 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|..
gi 119714219 452 SGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAMEHDL 513
PRK10651 154 NQLTPRERDILKLIAQGLSNKMIARRLDITESTVKVHVKHMLKKMKLKSRVEAAVWVHQERI 215
|
|
|
|
|
|
|
-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 |
22.09 |
4,156,234,33,189,269,4,193,276,5,198,282,28 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 119714219 157 IAQQFERWDGTGGPGGLAGVEITLAARVSEVAT--QALL---VHQEA-GVDAVMSMLRDRSGSWFDPSVVEACARH 226
COG2206 235 ALRHHERWDGTGYPRGLKGEEIPLEARIIAVADvyDALTsdrPYKKAkSPEEALEELRKNSGGKFDPKVVDAFLKA 310
|
|
|
|
|
|
|
-1 |
| 137869 |
PRK10403 |
PRK10403 |
transcriptional regulator NarP; Provisional |
transcriptional regulator NarP; Provisional |
false |
true |
false |
215 |
2e-06 |
49.47 |
32.56 |
2,436,141,10,451,151,60 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 119714219 437 EAAGEQPAPVrgnwpSGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAMEH 511
PRK10403 142 EMFGAEEDPF-----SVLTERELDVLHELAQGLSNKQIASVLNISEQTVKVHIRNLLRKLNVRSRVAATILFLQQ 211
|
|
|
|
|
|
|
-1 |
| 137688 |
PRK10100 |
PRK10100 |
DNA-binding transcriptional regulator CsgD; Provisional |
DNA-binding transcriptional regulator CsgD; Provisional |
false |
true |
false |
216 |
4e-05 |
44.55 |
26.85 |
1,453,155,58 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*...
gi 119714219 454 LSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYAMEH 511
PRK10100 156 LTHREKEILNKLRIGASNNEIARSLFISENTVKTHLYNLFKKIAVKNRTQAVSWANDN 213
|
|
|
|
|
|
|
-1 |
| 135188 |
PRK04841 |
PRK04841 |
transcriptional regulator MalT; Provisional |
transcriptional regulator MalT; Provisional |
false |
true |
false |
903 |
7e-05 |
43.82 |
6.31 |
1,451,836,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119714219 452 SGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAAALYA 508
PRK04841 837 SPLTQREWQVLGLIYSGYSNEQIAGELDVAATTIKTHIRNLYQKLGIAHRQEAVQLA 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 |
8e-05 |
44.00 |
25.86 |
1,444,162,60 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|
gi 119714219 445 PVRGNWPSGLSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAAA 504
TIGR03541 163 APLLREAGVLSEREREVLAWTALGRRQADIAAILGISERTVENHLRSARRKLGVATTAQA 222
|
|
|
|
|
|
|
-1 |
| 34204 |
COG4566 |
TtrR |
Response regulator [Signal transduction mechanisms] |
Response regulator [Signal transduction mechanisms] |
false |
true |
false |
202 |
2e-04 |
42.15 |
24.75 |
1,453,142,50 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|
gi 119714219 454 LSDREVEVLRLVAKGLSNQEVAQTLVISRRTAEHHVQHVYAKIGTSTRAA 503
COG4566 143 LTPRERQVLDLVVRGLMNKQIAFDLGISERTVELHRANVMEKMQARSLAE 192
|
|
|
|
|
|
|
-1 |