| 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-11 |
65.63 |
100.00 |
1,446,0,57 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*..
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFALR 503
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-08 |
55.08 |
99.31 |
3,268,0,49,324,49,25,349,81,63 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 269 PNRAGHSSGVAELAGSAASCLGLPAVDVAASRRAGYLHDIGLHGVPSTIldkpgalSATEWERVRVSSYYTERVLAQPAP 348
cd00077 1 EHRFEHSLRVAQLARRLAEELGLSEEDIELLRLAALLHDIGKPGTPDAI-------TEEESELEKDHAIVGAEILRELLL 73
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|.
gi 119717534 349 L-------ARIGAIASYTNERMDGSGYHRGASGASIPMAGRVLAAACALRTLTEPRVGRPPKSVKDAATEL 412
cd00077 74 EeviklidELILAVDASHHERLDGLGYPDGLKGEEITLEARIVKLADRLDALRRDSREKRRRIAEEDLEEL 144
|
|
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 |
6e-11 |
64.08 |
94.83 |
1,446,3,55 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFA 501
smart00421 4 LTPREREVLRLLAEGLTNKEIAERLGISEKTVKTHLSNIMRKLGVRSRTQAVRLA 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 |
1e-09 |
59.61 |
93.85 |
1,446,4,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFALRNGLL 507
COG2771 5 LTPREREILRLVAQGKSNKEIARILGISEETVKTHLRNIYRKLGVKNRVELVALALRLGLI 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 |
| 109261 |
pfam00196 |
GerE |
Bacterial regulatory proteins, luxR family |
Bacterial regulatory proteins, luxR family |
false |
false |
false |
58 |
1e-08 |
56.42 |
94.83 |
1,446,3,55 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFA 501
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 |
| 129378 |
TIGR00277 |
HDIG |
uncharacterized domain HDIG |
uncharacterized domain HDIG |
false |
false |
false |
80 |
0.002 |
39.62 |
41.25 |
2,273,7,17,293,24,16 |
10 20 30
....*....|....*....|....*....|....*.
gi 119717534 274 HSSGVAELAGSAASCLGlpaVDVAASRRAGYLHDIG 309
TIGR00277 8 HSLEVAKLAEALARELG---LDVELARRGALLHDIG 40
|
|
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 |
8e-31 |
130.26 |
48.26 |
3,264,142,81,345,224,68,414,292,16 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 265 DLRSPNRAGHSSGVAELAGSAASCLGLPAVDVAASRRAGYLHDIGLHGVPSTILDKPGALSATEWERVRVSSYYTERVLA 344
COG2206 143 KAKDDYTYGHSVRVAELAEAIAKKLGLSEEKIEELALAGLLHDIGKIGIPDSILNKPGKLTEEEFEIIKKHPIYGYDILK 222
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 345 Q-PAPLARIGAIASYTNERMDGSGYHRGASGASIPMAGRVLAAACALRTLTEPRVGRPPKSVKDAATELRsEVRAGRLDV 423
COG2206 223 DlPEFLESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDALTSDRPYKKAKSPEEALEELR-KNSGGKFDP 301
|
....*..
gi 119717534 424 DATDAVL 430
COG2206 302 KVVDAFL 308
|
|
|
|
|
|
|
-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 |
1e-22 |
102.68 |
43.33 |
3,264,179,90,354,270,61,417,331,4 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 265 DLRSPNRAGHSSGVAELAGSAASCLGLPAVDVAASRRAGYLHDIGLHGVPSTILDKPGALSATEWERVRVSSYYTERVLA 344
COG3437 180 EVRDYETGDHLERVAQYSELLAELLGLSEEEVDLIKKAAPLHDIGKVAIPDSILLKPGKLTSEEFEIMKGHPILGAEILK 259
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 119717534 345 QPAPLARIGA-IASYTNERMDGSGYHRGASGASIPMAGRVLAAACALRTLTEPRVGRPPKSVKDAATELRSEvrAGRL 421
COG3437 260 SSERLMQVAAeIARHHHERWDGSGYPDGLKGDEIPLSARIVAIADVFDALVSGRPYKEAMSTEEALEIIRAQ--SGRL 335
|
|
|
|
|
|
|
-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-12 |
67.67 |
29.86 |
1,446,148,63 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|...
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFALRNGLLDP 509
COG2197 149 LTPRELEVLRLLAEGLSNKEIAEELNLSEKTVKTHVSNILRKLGVRNRTEAAIRALRLGLIEA 211
|
|
|
|
|
|
|
-1 |
| 32733 |
COG2909 |
MalT |
ATP-dependent transcriptional regulator [Transcription] |
ATP-dependent transcriptional regulator [Transcription] |
false |
true |
false |
894 |
5e-07 |
51.07 |
6.82 |
1,446,831,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFALRNGLL 507
COG2909 832 LSQRELEVLGLIAQGLSNEEIAQELFISLTTVKTHIRNIYQKLGVANRTQAVQRAKELGLL 892
|
|
|
|
|
|
|
-1 |
| 139165 |
PRK12704 |
PRK12704 |
phosphodiesterase; Provisional |
phosphodiesterase; Provisional |
false |
true |
false |
455 |
3e-05 |
45.22 |
12.09 |
3,269,269,22,294,291,16,312,307,17 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 270 NRAGHSSGVAELAGSAASCLGLpavDVAASRRAGYLHDIGLhgVPSTILDKPGALSATEW 329
PRK12704 270 NVLQHSREVAHLAGLMAAELGL---DEKLAKRAGLLHDIGK--ALDHEVEGSHVELGVEL 324
|
|
|
|
|
|
|
-1 |
| 135188 |
PRK04841 |
PRK04841 |
transcriptional regulator MalT; Provisional |
transcriptional regulator MalT; Provisional |
false |
true |
false |
903 |
3e-05 |
45.36 |
5.65 |
1,446,838,51 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|.
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTA 497
PRK04841 839 LTQREWQVLGLIYSGYSNEQIAGELDVAATTIKTHIRNLYQKLGIAHRQEA 889
|
|
|
|
|
|
|
-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 |
7e-05 |
43.97 |
28.49 |
3,126,209,16,142,226,44,186,276,31 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 127 IQAHCLITSTLAERLG-LDDAVSAAVRQFFARWDGQGVPPHVGGEDLSPWVRLFHVGDITE------VYHRNGGVEAAVR 199
COG2206 210 IKKHPIYGYDILKDLPeFLESVRAVALRHHERWDGTGYPRGLKGEEIPLEARIIAVADVYDaltsdrPYKKAKSPEEALE 289
|
90
....*....|....*...
gi 119717534 200 VARERRGRQFDPALADAF 217
COG2206 290 ELRKNSGGKFDPKVVDAF 307
|
|
|
|
|
|
|
-1 |
| 132362 |
TIGR03319 |
YmdA_YtgF |
conserved hypothetical protein YmdA/YtgF |
conserved hypothetical protein YmdA/YtgF |
false |
true |
false |
514 |
1e-04 |
43.38 |
6.42 |
2,273,332,18,294,350,15 |
10 20 30
....*....|....*....|....*....|....*.
gi 119717534 274 HSSGVAELAGSAASCLGLpavDVAASRRAGYLHDIG 309
TIGR03319 333 HSIEVAHLAGIMAAELGE---DVKLAKRAGLLHDIG 365
|
|
|
|
|
|
|
-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 |
1,446,171,59 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*....
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFALRNG 505
TIGR03541 172 LSEREREVLAWTALGRRQADIAAILGISERTVENHLRSARRKLGVATTAQAIAIALRKG 230
|
|
|
|
|
|
|
-1 |
| 137324 |
PRK09483 |
PRK09483 |
response regulator; Provisional |
response regulator; Provisional |
false |
true |
false |
216 |
3e-04 |
41.63 |
29.17 |
1,446,148,63 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|...
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFALRNGLLDP 509
PRK09483 149 LSERELQIMLMITKGQKVNEISEQLNLSPKTVNSYRYRMFSKLNISGDVELTHLAIRHGLLNA 211
|
|
|
|
|
|
|
-1 |
| 137598 |
PRK09935 |
PRK09935 |
transcriptional regulator FimZ; Provisional |
transcriptional regulator FimZ; Provisional |
false |
true |
false |
210 |
4e-04 |
41.42 |
22.38 |
1,446,149,47 |
10 20 30 40
....*....|....*....|....*....|....*....|....*..
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACS 493
PRK09935 150 LSNREVTVLRYLANGLSNKEIAEQLLLSNKTISAHKSNIYGKLGLHS 196
|
|
|
|
|
|
|
-1 |
| 139166 |
PRK12705 |
PRK12705 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
485 |
5e-04 |
41.24 |
6.80 |
2,273,302,18,294,320,15 |
10 20 30
....*....|....*....|....*....|....*.
gi 119717534 274 HSSGVAELAGSAASCLGLpavDVAASRRAGYLHDIG 309
PRK12705 303 HSLEVAFLAAILAALIGL---DPALAKKAGLLHDIG 335
|
|
|
|
|
|
|
-1 |
| 137869 |
PRK10403 |
PRK10403 |
transcriptional regulator NarP; Provisional |
transcriptional regulator NarP; Provisional |
false |
true |
false |
215 |
9e-04 |
40.23 |
26.05 |
1,446,153,56 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....*.
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACSRSTATLFAL 502
PRK10403 154 LTERELDVLHELAQGLSNKQIASVLNISEQTVKVHIRNLLRKLNVRSRVAATILFL 209
|
|
|
|
|
|
|
-1 |
| 138058 |
PRK10651 |
PRK10651 |
transcriptional regulator NarL; Provisional |
transcriptional regulator NarL; Provisional |
false |
true |
false |
216 |
0.001 |
40.05 |
34.72 |
2,408,138,16,445,154,59 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 119717534 409 ATELRSEVRAGRLDVDatdavlsaagaggrrrvagpaGLTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAK 488
PRK10651 139 AASLRANRATTERDVN---------------------QLTPRERDILKLIAQGLSNKMIARRLDITESTVKVHVKHMLKK 197
|
90
....*....|....*.
gi 119717534 489 TGACSRSTATLFALRN 504
PRK10651 198 MKLKSRVEAAVWVHQE 213
|
|
|
|
|
|
|
-1 |
| 134107 |
PRK00106 |
PRK00106 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
535 |
0.003 |
38.72 |
6.17 |
2,273,353,17,293,370,16 |
10 20 30
....*....|....*....|....*....|....*.
gi 119717534 274 HSSGVAELAGSAASCLGlpaVDVAASRRAGYLHDIG 309
PRK00106 354 HSVEVGKLAGILAGELG---ENVALARRAGFLHDMG 386
|
|
|
|
|
|
|
-1 |
| 34204 |
COG4566 |
TtrR |
Response regulator [Signal transduction mechanisms] |
Response regulator [Signal transduction mechanisms] |
false |
true |
false |
202 |
0.005 |
37.91 |
23.27 |
1,446,142,47 |
10 20 30 40
....*....|....*....|....*....|....*....|....*..
gi 119717534 447 LTQREVEVLVLIARGVATNEVAARLGVSRKTAATHIERIYAKTGACS 493
COG4566 143 LTPRERQVLDLVVRGLMNKQIAFDLGISERTVELHRANVMEKMQARS 189
|
|
|
|
|
|
|
-1 |
| 31608 |
COG1418 |
COG1418 |
Predicted HD superfamily hydrolase [General function prediction only] |
Predicted HD superfamily hydrolase [General function prediction only] |
false |
true |
false |
222 |
0.010 |
36.97 |
17.57 |
2,267,33,23,293,56,16 |
10 20 30 40
....*....|....*....|....*....|....*....|..
gi 119717534 268 SPNRAGHSSGVAELAGSAASCLGlpaVDVAASRRAGYLHDIG 309
COG1418 34 GQHVLEHSLRVAYLAYRIAEEEG---VDPDLALRAALLHDIG 72
|
|
|
|
|
|
|
-1 |