| 28956 |
cd00075 |
HATPase_c |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for example: histidine kinase, DNA gyrase B, topoisomerases, heat shock protein HSP90, phytochrome-like ATPases and DNA mismatch repair proteins |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for... |
true |
false |
true |
103 |
1e-11 |
66.50 |
91.26 |
3,365,9,10,375,20,37,414,57,46 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 366 DNARKYTPES-GYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFyrVDKARSRGEGGAGLGLSLAKWIAGQHKTEI 444
cd00075 10 SNAIKHTPEGgGRITISVERDGDHLEIRVEDNGPGIPEEDLERIFERF--SDGSRSRKGGGTGLGLSIVKKLVELHGGRI 87
|
90
....*....|....*.
gi 94967341 445 HVESTPGAGSTFSFRL 460
cd00075 88 EVESEPGGGTTFTITL 103
|
|
cl00075 |
140416 |
HATPase_c |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for example: histidine kinase, DNA gyrase B, topoisomerases, heat shock protein HSP90, phytochrome-like ATPases and DNA mismatch repair proteins |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for... |
0 |
| 119399 |
cd00082 |
HisKA |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are formed through parallel association of 2 domains creating 4-helix bundles; usually these domains contain a conserved His residue and are activated via trans-autophosphorylation by the catalytic domain of the histidine kinase. They subsequently transfer the phosphoryl group to the Asp acceptor residue of a response regulator protein. Two-component signalling systems, consisting of a histidine protein kinase that senses a signal input and a response regulator that mediates the output, are ancient and evolutionarily conserved signaling mechanisms in prokaryotes and eukaryotes. |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are... |
true |
false |
true |
65 |
1e-11 |
66.08 |
93.85 |
1,241,4,61 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|.
gi 94967341 242 RQFTADASHELRTPLSLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLAR 302
cd00082 5 GEFLANVSHELRTPLTAIRGALELLEEELLDDEEQREYLERIREEAERLLRLINDLLDLSR 65
|
|
cl00080 |
140419 |
HisKA |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are formed through parallel association of 2 domains creating 4-helix bundles; usually these domains contain a conserved His residue and are activated via trans-autophosphorylation by the catalytic domain of the histidine kinase. They subsequently transfer the phosphoryl group to the Asp acceptor residue of a response regulator protein. Two-component signalling systems, consisting of a histidine protein kinase that senses a signal input and a response regulator that mediates the output, are ancient and evolutionarily conserved signaling mechanisms in prokaryotes and eukaryotes. |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are... |
3 |
| 128669 |
smart00387 |
HATPase_c |
Histidine kinase-like ATPases |
Histidine kinase-like ATPases |
false |
false |
false |
111 |
3e-17 |
85.01 |
84.68 |
2,365,14,69,435,83,25 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 366 DNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKwIAGQHKTEIH 445
smart00387 15 DNAIKYTPEGGRITVTLERDGDHLEITVEDNGPGIPPEDLEKIFEPFFRTDGRSRKIGGTGLGLSIVKK-LVELHGGEIS 93
|
90
....*....|....*
gi 94967341 446 VESTPGAGSTFSFRL 460
smart00387 94 VESEPGGGTTFTITL 108
|
|
cl00075 |
140416 |
HATPase_c |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for example: histidine kinase, DNA gyrase B, topoisomerases, heat shock protein HSP90, phytochrome-like ATPases and DNA mismatch repair proteins |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for... |
-1 |
| 111420 |
pfam02518 |
HATPase_c |
Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase |
Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase |
false |
false |
false |
111 |
4e-15 |
77.75 |
84.68 |
2,365,14,69,435,83,25 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 366 DNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKwIAGQHKTEIH 445
pfam02518 15 DNAIKHAPAGGEITVTLEREGGRLRITVEDNGPGIPPEDLEKIFEPFYRDGSDSRKVGGTGLGLSIVKK-LVELHGGTIT 93
|
90
....*....|....*
gi 94967341 446 VESTPGAGSTFSFRL 460
pfam02518 94 VESEPGGGTTFTLTL 108
|
|
cl00075 |
140416 |
HATPase_c |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for example: histidine kinase, DNA gyrase B, topoisomerases, heat shock protein HSP90, phytochrome-like ATPases and DNA mismatch repair proteins |
Histidine kinase-like ATPases; This family includes several ATP-binding proteins for... |
-1 |
| 128670 |
smart00388 |
HisKA |
His Kinase A (phosphoacceptor) domain |
His Kinase A (phosphoacceptor) domain |
false |
false |
false |
66 |
2e-10 |
62.21 |
96.97 |
2,241,2,34,276,36,30 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 94967341 242 RQFTADASHELRTPLSLIRTEAELALRKTRTEEEyRNALGHVLAESERTTELIESLLTLARTDSG 306
smart00388 3 REFLANLSHELRTPLTAIRGYLELLEDTELSEEQ-REYLETILRSAERLLRLINDLLDLSRIEAG 66
|
|
cl00080 |
140419 |
HisKA |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are formed through parallel association of 2 domains creating 4-helix bundles; usually these domains contain a conserved His residue and are activated via trans-autophosphorylation by the catalytic domain of the histidine kinase. They subsequently transfer the phosphoryl group to the Asp acceptor residue of a response regulator protein. Two-component signalling systems, consisting of a histidine protein kinase that senses a signal input and a response regulator that mediates the output, are ancient and evolutionarily conserved signaling mechanisms in prokaryotes and eukaryotes. |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are... |
-1 |
| 109563 |
pfam00512 |
HisKA |
His Kinase A (phosphoacceptor) domain |
His Kinase A (phosphoacceptor) domain |
false |
false |
false |
66 |
3e-10 |
61.81 |
96.97 |
2,241,2,34,276,36,30 |
10 20 30 40 50 60
....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 94967341 242 RQFTADASHELRTPLSLIRTEAELALRKTRTEEEyRNALGHVLAESERTTELIESLLTLARTDSG 306
pfam00512 3 SEFLANLSHELRTPLTAIRGYLELLLDTELSEEQ-REYLETILRSAERLLRLINDLLDLSRIEAG 66
|
|
cl00080 |
140419 |
HisKA |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are formed through parallel association of 2 domains creating 4-helix bundles; usually these domains contain a conserved His residue and are activated via trans-autophosphorylation by the catalytic domain of the histidine kinase. They subsequently transfer the phosphoryl group to the Asp acceptor residue of a response regulator protein. Two-component signalling systems, consisting of a histidine protein kinase that senses a signal input and a response regulator that mediates the output, are ancient and evolutionarily conserved signaling mechanisms in prokaryotes and eukaryotes. |
Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are... |
-1 |
| 109717 |
pfam00672 |
HAMP |
HAMP domain |
HAMP domain |
true |
false |
false |
70 |
1e-06 |
49.92 |
100.00 |
2,165,0,48,214,48,22 |
10 20 30 40 50 60 70
....*....|....*....|....*....|....*....|....*....|....*....|....*....|.
gi 94967341 166 FLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIHERNLNQRLPPlQTNDELQRLSDTLNEMLSRIEA 236
pfam00672 1 LLLVLLIALLLLLLLAWLLARRLLRPLRRLAEAARRIASGDLDDRVPV-SGPDEIGELARAFNQMADRLRE 70
|
|
cl01054 |
141075 |
HAMP |
Histidine kinase, Adenylyl cyclase, Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain which occurs in a wide variety of signaling proteins, many of which are bacterial. The HAMP domain consists of two alpha helices connected by an extended linker. The structure of the HAMP dimer from Archaeoglobus fulgidus has been solved using nuclear magnetic resonance, revealing a parallel four-helix bundle; this structure has been confirmed by cross-linking analysis of HAMP domains from the Escherichia coli aerotaxis receptor Aer. It has been suggested that the four-helix arrangement can rotate between the unusually packed conformation observed in the NMR structure and a canonical coiled-coil arrangement. Such rotation may coincide with signal transduction, but a common mechanism by which HAMP domains relay a variety of input signals has yet to be established. |
Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain... |
-1 |
| 128599 |
smart00304 |
HAMP |
HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain |
HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain |
false |
false |
false |
53 |
3e-04 |
41.86 |
100.00 |
2,185,0,28,214,28,25 |
10 20 30 40 50
....*....|....*....|....*....|....*....|....*....|....
gi 94967341 186 RRALRSVDEITAMARSIHERNLNQRLPPlQTNDELQRLSDTLNEMLSRIEAAFT 239
smart00304 1 RRILRPLRRLAEAAQRIADGDLTVRLPV-DGRDEIGELARAFNEMADRLEETIA 53
|
|
cl01054 |
141075 |
HAMP |
Histidine kinase, Adenylyl cyclase, Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain which occurs in a wide variety of signaling proteins, many of which are bacterial. The HAMP domain consists of two alpha helices connected by an extended linker. The structure of the HAMP dimer from Archaeoglobus fulgidus has been solved using nuclear magnetic resonance, revealing a parallel four-helix bundle; this structure has been confirmed by cross-linking analysis of HAMP domains from the Escherichia coli aerotaxis receptor Aer. It has been suggested that the four-helix arrangement can rotate between the unusually packed conformation observed in the NMR structure and a canonical coiled-coil arrangement. Such rotation may coincide with signal transduction, but a common mechanism by which HAMP domains relay a variety of input signals has yet to be established. |
Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain... |
-1 |
| 100122 |
cd06225 |
HAMP |
Histidine kinase, Adenylyl cyclase, Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain which occurs in a wide variety of signaling proteins, many of which are bacterial. The HAMP domain consists of two alpha helices connected by an extended linker. The structure of the HAMP dimer from Archaeoglobus fulgidus has been solved using nuclear magnetic resonance, revealing a parallel four-helix bundle; this structure has been confirmed by cross-linking analysis of HAMP domains from the Escherichia coli aerotaxis receptor Aer. It has been suggested that the four-helix arrangement can rotate between the unusually packed conformation observed in the NMR structure and a canonical coiled-coil arrangement. Such rotation may coincide with signal transduction, but a common mechanism by which HAMP domains relay a variety of input signals has yet to be established. |
Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain... |
false |
false |
false |
48 |
0.002 |
39.16 |
97.92 |
2,188,1,25,214,26,22 |
10 20 30 40
....*....|....*....|....*....|....*....|....*...
gi 94967341 189 LRSVDEITAMARSIHERNLNQRLPPlQTNDELQRLSDTLNEMLSRIEA 236
cd06225 2 LRPLRRLAEAAQRIAAGDLDVRLPV-TGRDEIGELARAFNQMAERLRE 48
|
|
cl01054 |
141075 |
HAMP |
Histidine kinase, Adenylyl cyclase, Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain which occurs in a wide variety of signaling proteins, many of which are bacterial. The HAMP domain consists of two alpha helices connected by an extended linker. The structure of the HAMP dimer from Archaeoglobus fulgidus has been solved using nuclear magnetic resonance, revealing a parallel four-helix bundle; this structure has been confirmed by cross-linking analysis of HAMP domains from the Escherichia coli aerotaxis receptor Aer. It has been suggested that the four-helix arrangement can rotate between the unusually packed conformation observed in the NMR structure and a canonical coiled-coil arrangement. Such rotation may coincide with signal transduction, but a common mechanism by which HAMP domains relay a variety of input signals has yet to be established. |
Methyl-accepting protein, and Phosphatase (HAMP) domain. HAMP is a signaling domain... |
-1 |
| 130453 |
TIGR01386 |
cztS_silS_copS |
heavy metal sensor kinase |
heavy metal sensor kinase |
true |
true |
false |
457 |
2e-46 |
182.20 |
99.34 |
9,5,3,52,60,55,22,82,80,14,97,94,43,140,140,23,163,164,17,181,181,160,344,341,108,453,449,8 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 6 IRIRLTLWYAGIFTLALVAFGSSVWVLVRERLNDEVQDQLELRVAGVQRFMAaqsSGATLEDMRRALEEEYETEDHA--- 82
TIGR01386 4 LTLRLALLFAAVTALVFALSGFMLYSSLERHFEERDREELQGKLEQVRRFLR---DPADLDEDIKRLQEKIDDLLVGhsd 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 83 VWLQVLDQDGNWMFrARGMADTFPSPSLPRELSPKGRISTGRDGRFHVLMLQKAVSVQ---DRLYTIEAGASTNGIHHTL 159
TIGR01386 81 LALSILNPDGRLLF-ERAQGAALVPAVAANDALLELDQADAKMTHYRSILRSVAALPGgkgRKPVQITVALDINAHTHLL 159
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 160 EQLR-NVFLFLVPCFVLIAAVGsYYFSRRALRSVDEITAMARSIHERNLNQRLPPLQTNDELQRLSDTLNEMLSRIEAAF 238
TIGR01386 160 DALRkWLILIAVLLVLLTALLG-WWITRLGLEPLRRLSAVAARISPESLDQRLDPSRAPAELRELAQSFNAMLGRLEDAF 238
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 239 TRTRQFTADASHELRTPLSLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTN 318
TIGR01386 239 QRLSQFSADLAHELRTPLTNLLGQTQVALSQPRTGEEYREVLESNLEELERLSRMVSDMLFLARADNGQLALERVRLDLA 318
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 319 TFLRHCTEEWAQVMGEARLRLEValpSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGC 398
TIGR01386 319 AELAKVAEYFEPLAEERGVRIRV---EGEGLVRGDPQMFRRAISNLLSNALRHTPDGGTITVRIERRSDEVRVSVSNPGP 395
|
410 420 430 440 450 460
....*....|....*....|....*....|....*....|....*....|....*....|...
gi 94967341 399 GIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAgSTFSFRLA 461
TIGR01386 396 GIPPEHLSRLFDRFYRVDPARSNSGEGTGLGLAIVRSIMEAHGGRASAESPDGK-TRFILRFP 457
|
|
|
|
|
|
|
-1 |
| 137545 |
PRK09835 |
PRK09835 |
sensor kinase CusS; Provisional |
sensor kinase CusS; Provisional |
false |
true |
false |
482 |
6e-34 |
140.36 |
70.33 |
9,103,128,21,129,149,13,142,163,22,164,191,15,182,206,10,195,216,111,310,327,12,322,342,14,337,356,111 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 104 TFPSPSLPRELSPKGRISTGRdgrfhVLMLQKAVSVQDR-LYTIEAGASTNGIHHTLEQLRN------VFLFLVPCFVLI 176
PRK09835 129 SGPTPMMPGHGHGHMEHSNWR-----MINLPVGPLVDGKpIYTLYIALSIDFHLHYINDLMNklimtaSVISILIVFIVL 203
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 177 AAVgsyYFSRRALRSVdeiTAMARSIHERNLNQRLPPLQTNDELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPL 256
PRK09835 204 LAV---HKGHAPIRSV---SRQIQNITSKDLDVRLDPQTVPIELEQLVLSFNHMIERIEDVFTRQSNFSADIAHEIRTPI 277
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 257 SLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSGaeiiQLVPLQTNTFLR---HCTEEWAQVMG 333
PRK09835 278 TNLITQTEIALSQSRSQKELEDVLYSNLEELTRMAKMVSDMLFLAQADNN----QLIPEKKMLNLAdevGKVFDFFEALA 353
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 334 EARlRLEVALPSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFY 413
PRK09835 354 EDR-GVELRFVGDPCQVAGDPLMLRRALSNLLSNALRYTPEGEAIVVRCQTVDHQVQVVVENPGTPIAPEHLPRLFDRFY 432
|
330 340 350
....*....|....*....|....*....|....*
gi 94967341 414 RVDKARSRGEGGAGLGLSLAKWIAGQHKTEIHVES 448
PRK09835 433 RVDPSRQRKGEGSGIGLAIVKSIVVAHKGTVAVTS 467
|
|
|
|
|
|
|
-1 |
| 132011 |
TIGR02966 |
phoR_proteo |
phosphate regulon sensor kinase PhoR |
phosphate regulon sensor kinase PhoR |
false |
true |
false |
333 |
7e-34 |
140.04 |
65.77 |
3,241,114,32,273,147,70,344,217,116 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 242 RQFTADASHELRTPLSLIRTEAELALRKTRTE-EEYRNALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTNTF 320
TIGR02966 115 RDFVANVSHELRTPLTVLRGYLETLADGPDEDpEEWNRALEIMLEQSQRMQSLVEDLLTLSRLESAASPLEDEPVDMPAL 194
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 321 LRHCTEEWAQVMGEARLRLEVALpSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGCGI 400
TIGR02966 195 LDHLRDEAEALSQGKNHQITFEI-DGGVDVLGDEDELRSAFSNLVSNAIKYTPEGGTITVRWRRDGGGAEFSVTDTGIGI 273
|
170 180 190 200 210 220
....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 401 QAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRL 460
TIGR02966 274 APEHLPRLTERFYRVDKSRSRDTGGTGLGLAIVKHVLSRHHARLEIESELGKGSTFSFIF 333
|
|
|
|
|
|
|
-1 |
| 30987 |
COG0642 |
BaeS |
Signal transduction histidine kinase [Signal transduction mechanisms] |
Signal transduction histidine kinase [Signal transduction mechanisms] |
false |
true |
false |
336 |
1e-30 |
129.52 |
88.69 |
8,154,29,48,204,77,38,242,116,26,270,142,39,309,182,35,345,217,29,375,246,42,421,288,39 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 155 IHHTLEQLRNVFLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIheRNLNQRLPPLQTNDELQRLSDTLNEMLSRI 234
COG0642 30 LAVARNELLLLLLLTLLAALLVALLLLLLLLRRLLRPLLLLADAANAL--AAGLTRLVLASLGSELASLAHALNELLERL 107
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 235 EAAFTRTR-QFTADASHELRTPLSLIRTEAELALRktRTEEEYRNALGHVLAESERTTELIESLLTLARTDSGAEI-IQL 312
COG0642 108 ERLLRRAKrEFLANISHELRTPLTAIRGLLELLLE--GLLDPQRELLEIIEEEAERLLRLVNDLLDLSRLEAGTKLkLLL 185
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 313 VPLQTNTFLRHCTEEWAQVMGEARLRLEVALPsEETWVSADERLLRRLMVVLLDNARKYTPEsGYVRVFAELTDREVTVG 392
COG0642 186 ELVDLAELLEEVVRLLAPLAQEKGIELAVDLP-ELPYVLGDPERLRQVLVNLLSNAIKYTPG-GEITISVRQDDEQVTIS 263
|
250 260 270 280 290 300
....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 94967341 393 VQDNGCGIQAEHLPRIFDRFYRVDKarsrGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRL 460
COG0642 264 VEDTGPGIPEEELERIFEPFFRTDK----SRSGTGLGLAIVKRIVELHGGTISVESEPGKGTTFTIRL 327
|
|
|
|
|
|
|
-1 |
| 34607 |
COG5002 |
VicK |
Signal transduction histidine kinase [Signal transduction mechanisms] |
Signal transduction histidine kinase [Signal transduction mechanisms] |
false |
true |
false |
459 |
1e-26 |
116.19 |
48.15 |
4,241,225,23,265,248,11,276,261,66,342,328,118 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 242 RQFTADASHELRTPLSLIRTEAElALRKTRTEEEY--RNALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTNT 319
COG5002 226 REFVANVSHELRTPLTSMKSYLE-ALEEGAWEDKEiaPRFLRVTLNETERMIRLVNDLLQLSRMDNARYQLNKEWINFTA 304
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 320 FLRHCTEEWAQVMGEARLRLEVA-LPSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGC 398
COG5002 305 FLNEIINRFEMILKKETIARFVRdIPKQDIWVEIDPDKMTQVLDNIISNALKYSPDGGRITVSVKQRETWVEISISDQGL 384
|
170 180 190 200 210 220
....*....|....*....|....*....|....*....|....*....|....*....|..
gi 94967341 399 GIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRL 460
COG5002 385 GIPKEDLEKIFDRFYRVDKARSRKMGGTGLGLAIAKEIVQAHGGRIWAESEEGKGTTFSFTL 446
|
|
|
|
|
|
|
-1 |
| 137828 |
PRK10337 |
PRK10337 |
sensor protein QseC; Provisional |
sensor protein QseC; Provisional |
false |
true |
false |
446 |
3e-24 |
108.33 |
47.76 |
5,204,190,8,212,202,5,217,210,163,382,373,8,392,381,22 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 205 RNLNQRLP----PLQTN---DELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPLSLIRTEAELALRKTRTEEEYR 277
PRK10337 191 LALRMRDPdsetPLDATgvpSEVRPLVEALNQLFARTHAMMVRERRFTSDAAHELRSPLTALKVQTEVAQLSDDDPQARK 270
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 278 NALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTNTFLRHCTEEWAQVMGEARLRLEVALPSEETWVSADERLL 357
PRK10337 271 KALLQLHSGIDRATRLVDQLLTLSRLDSLDNLQDVAEIPLEDLLQSAVMDIYHTAQQAKIDVRLTLNAHGIKRTGQPLLL 350
|
170 180 190 200 210
....*....|....*....|....*....|....*....|....*....|....*..
gi 94967341 358 RRLMVVLLDNARKYTPESGYVRVfaELTDREVTvgVQDNGCGIQAEHLPRIFDRFYR 414
PRK10337 351 SLLVRNLLDNAVRYSPQGSVVDV--TLNARNFT--VRDNGPGVTPEALARIGERFYR 403
|
|
|
|
|
|
|
-1 |
| 138403 |
PRK11100 |
PRK11100 |
sensory histidine kinase CreC; Provisional |
sensory histidine kinase CreC; Provisional |
false |
true |
false |
475 |
2e-23 |
105.71 |
48.63 |
8,173,194,19,195,213,9,207,222,5,212,228,24,241,252,6,247,262,18,266,280,78,346,358,67 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 174 VLIAAVGSYYFSRRALRSVdeiTAMARSIHErnlNQRLP-PLQTNDELQRLSDTLNEMLSRIEAaftrtRQFTAD----A 248
PRK11100 195 ALLIGAGMVWWLNRSIRRL---TRYADAVAE---GKPVPlPKLGSSELRDLAQALESMRVKLEG-----KAYVEQyvqtL 263
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 249 SHELRTPLSLIRTEAELaLRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTNTFLRHCTEEW 328
PRK11100 264 THELKSPLAAIRGAAEL-LQEDPPPEDRQRFTGNILAQSARLQQLIDRLLELARLEQRQELEVLEPVALAALLEELVEAR 342
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 329 AQVMGEARLRLEVALPseETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRI 408
PRK11100 343 EAQAAAKGITLRLRPD--DAAVLGDPFLLRQALGNLLDNAIDFTPEGGTITLSAERDGEQVALSVEDSGPGIPDYALPRI 420
|
....*
gi 94967341 409 FDRFY 413
PRK11100 421 FERFY 425
|
|
|
|
|
|
|
-1 |
| 32387 |
COG2205 |
KdpD |
Osmosensitive K+ channel histidine kinase [Signal transduction mechanisms] |
Osmosensitive K+ channel histidine kinase [Signal transduction mechanisms] |
false |
true |
false |
890 |
2e-23 |
105.71 |
26.97 |
6,218,638,23,242,661,22,264,685,52,316,741,9,331,750,86,419,836,42 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 219 ELQRLSDTLNEMLSRIEAAFTRTrQFTADASHELRTPLSLIRTEAE--LALRKTRTEEEYRNALGHVLAESERTTELIES 296
COG2205 639 ERVTLAEEAEQARLAAERERLRS-ALLASISHDLRTPLTAIMGAAEtlLLDGEALSPEDRAELLSSIREESERLTRLVTN 717
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 297 LLTLARTDSGAEIIQLVPLQ----TNTFLRHCTeewaqvMGEARLRLEVALPSEETWVSADERLLRRLMVVLLDNARKYT 372
COG2205 718 LLDMTRLQSGGVNLKLDWVLveevVGEALQRLR------KRFTGHKIVVSVPVDLPLIHVDSPLIEQVLINLLENALKYA 791
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 373 PESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKarSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGA 452
COG2205 792 PPGSEIRINAGVERENVVFSVIDEGPGIPEGELERIFDKFYRGNK--ESATRGVGLGLAICRGIVEAHGGTISAENNPGG 869
|
....*....
gi 94967341 453 GSTFSFRLA 461
COG2205 870 GAIFVFTLP 878
|
|
|
|
|
|
|
-1 |
| 138336 |
PRK11006 |
phoR |
phosphate regulon sensor protein; Provisional |
phosphate regulon sensor protein; Provisional |
false |
true |
false |
431 |
5e-22 |
100.94 |
52.67 |
8,241,204,64,306,268,6,312,279,3,319,282,8,328,290,8,336,300,5,344,305,118,462,425,6 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 242 RQFTADASHELRTPLSLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSgAEIIQL-----VPLq 316
PRK11006 205 RNFFANVSHELRTPLTVLQGYLEMMEEQPLEGPMREKALHTMREQTQRMEGLVKQLLTLSKIEA-APTHLLnekvdVPM- 282
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 317 tntFLRHCTEEwAQVMGEAR--LRLEValpSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQ 394
PRK11006 283 ---MLRVLERE-AQTLSQKKhtITFEV---DDSLKVLGNEDQLRSAISNLVYNAVNHTPEGTHITVRWQRVPHGAEFSVE 355
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 94967341 395 DNGCGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRLAR--VANNTA 468
PRK11006 356 DNGPGIAPEHIPRLTERFYRVDKARSRQTGGSGLGLAIVKHALNHHDSRLEIESTVGKGTRFSFVLPErlIAKNSD 431
|
|
|
|
|
|
|
-1 |
| 138021 |
PRK10604 |
PRK10604 |
sensor protein RstB; Provisional |
sensor protein RstB; Provisional |
false |
true |
false |
433 |
3e-19 |
91.67 |
57.97 |
8,198,170,12,210,184,3,216,187,39,257,226,18,276,244,12,291,256,50,343,306,29,374,335,86 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 199 ARSIHERNLNQR--LPPlqtNDELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPlsLIRTEAELALRKTRTEEEy 276
PRK10604 171 AQRFGDGHLSERihFDP---GSSFERLGVAFNQMADNINALIASKKQLIDGIAHELRTP--LVRLRYRLEMSDNLSAAE- 244
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 277 RNALGHVLAESErttELIESLLTLARTDSGAEIIQLVPLQTNTFLRHCTEEWAQVMGEARLRLEValPSEETWVSADERL 356
PRK10604 245 SQALNRDIGQLE---ALIEELLTYARLDRPQNELHLSEPDLPAWLSTHLADIQAVTPEKTVRLKT--PHQGDYGALDMRL 319
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 357 LRRLMVVLLDNARKYTpeSGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWI 436
PRK10604 320 MERVLDNLLNNALRYS--HSTVETSLLLDGDQATLIVEDDGPGIAPEERERIFEPFVRLDPSRDRATGGCGLGLAIVHSI 397
|
250 260
....*....|....*....|....
gi 94967341 437 AGQHKTEIHVESTPGAGSTFSFRL 460
PRK10604 398 ALAMGGSVNCDTSELGGARFSFSW 421
|
|
|
|
|
|
|
-1 |
| 137977 |
PRK10549 |
PRK10549 |
signal transduction histidine-protein kinase BaeS; Provisional |
signal transduction histidine-protein kinase BaeS; Provisional |
false |
true |
false |
467 |
3e-18 |
88.24 |
61.88 |
5,160,161,53,214,214,51,265,268,8,278,276,66,345,342,108 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 161 QLRNVFLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIHERNLNQRLPPlQTNDELQRLSDTLNEMLSRIEAAFTR 240
PRK10549 162 QQRRTSWLIVALSTLLAALATFLLARGLLAPVKRLVEGTHKLAAGDFTTRVTP-TSEDELGKLAQDFNQLASTLEKNQQM 240
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 241 TRQFTADASHELRTPLSLIRTEAEL---ALRKTRTEeeyrnALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQT 317
PRK10549 241 RRDFMADISHELRTPLAVLRGELEAiqdGVRKFTPE-----SVASLQAEVGTLTKLVDDLHQLSLSDEGALAYQKTPVDL 315
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 318 NTFLRHCTEEWAQVMGEARLRLEVALPsEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNG 397
PRK10549 316 VPLLEVAGGAFRERFASRGLTLQFSLP-DSATVFGDPDRLMQLFNNLLENSLRYTDSGGSLHISAEQHDKTLRLTFADSA 394
|
250 260 270 280 290
....*....|....*....|....*....|....*....|....*....|....*.
gi 94967341 398 CGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAG 453
PRK10549 395 PGVSDEQLQKLFERFYRTEGSRNRASGGSGLGLAICLNIVEAHNGRIIAAHSPFGG 450
|
|
|
|
|
|
|
-1 |
| 33974 |
COG4251 |
COG4251 |
Bacteriophytochrome (light-regulated signal transduction histidine kinase) [Signal transduction mechanisms] |
Bacteriophytochrome (light-regulated signal transduction histidine kinase) [Signal... |
false |
true |
false |
750 |
2e-15 |
79.22 |
31.33 |
6,221,504,49,270,555,47,319,602,27,349,629,22,371,652,44,417,696,43 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 222 RLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPLSLIRTEAELALRKT--RTEEEYRNALGHVLAESERTTELIESLLT 299
COG4251 505 RHAEELAQLRRELERSNAELRAFAYVASHDLQEPLRQISNYAQLLSERYsdALDEEAKEFITFISRLTSLMQQLIDDLLT 584
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 300 LARTDSGAEIIQLVPLQTntFLRHCTEEWAQVMGEARLRLEVALPSEetwVSADERLLRRLMVVLLDNARKY-TPESGYV 378
COG4251 585 YSKLGLTEAPLQPTDVQK--VVDKVLLELSQRIADTGAEIRIAPLPV---VAADATQLGQVFQNLIANAIKFgGPENPDI 659
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 379 RVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVdkARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSF 458
COG4251 660 EISAERQEDEWTFSVRDNGIGIDPAYFERIFVIFQRL--HSRDEYLGTGLGLAICKKIAERHQGRIWVESTPGEGSTFYF 737
|
..
gi 94967341 459 RL 460
COG4251 738 TL 739
|
|
|
|
|
|
|
-1 |
| 138539 |
PRK11360 |
PRK11360 |
sensory histidine kinase AtoS; Provisional |
sensory histidine kinase AtoS; Provisional |
false |
true |
false |
607 |
2e-14 |
75.50 |
34.43 |
5,244,391,21,266,412,39,309,451,71,380,523,33,419,556,44 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 245 TADASHELRTPLSLIRTEAELaLRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSgaeiIQLVPLQTNTFLRHC 324
PRK11360 392 MAGVAHEIRNPLTAIRGYVQI-LRQQTSDPIHQEYLSVVLREVDSLNKVIQQLLEFSRPRH----SQWQQVSLNALVEEV 466
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 325 TEEWAQVMGEARLRLEVALPSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRV-FAELTDREVTVGVQDNGCGIQAE 403
PRK11360 467 LVLVQTAGVQARVDFITELDNELPPINADRELLKQVLLNILINAVQAISARGKIRIrTWQYSDSQQAISIEDNGCGIDLE 546
|
170 180 190 200 210 220
....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 404 HLPRIFDRFYrvdkarSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRLARV 463
PRK11360 547 LLKKIFDPFF------TTKASGTGLGLALSQRIINAHQGDIRVASLPGYGTTFTLILPIN 600
|
|
|
|
|
|
|
-1 |
| 33926 |
COG4191 |
COG4191 |
Signal transduction histidine kinase regulating C4-dicarboxylate transport system [Signal transduction mechanisms] |
Signal transduction histidine kinase regulating C4-dicarboxylate transport system [... |
false |
true |
false |
603 |
2e-13 |
72.61 |
51.91 |
10,158,290,29,187,320,27,214,362,13,233,375,4,237,380,24,261,407,17,279,424,28,311,452,61,372,515,67,443,582,21 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 159 LEQLRNVFLFLVPCFVLIAAVGSYYFSRR-ALRSVDEITAMARSIHERNLNQRLPPL---------------QTNDELQR 222
COG4191 291 RSAVRTARLAAILTLALLALLLALWLRRRrRARLRLAELQEARAELERRVEERTADLtranarlqaeiaereQAEAALRR 370
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 223 LSDTLnemlsrIEAA-FTRTRQFTADASHELRTPLSLIRT---EAELALRKTRTEEEYRNaLGHVLAESERTTELIESLL 298
COG4191 371 AQDEL------VQAGkLAALGQMSAGIAHELNQPLAAIRTyadNARLLLERGRTEEAREN-LERISALTERMAAITAHLK 443
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 299 TLARTDSGAeiiqLVPLQTNTFLRHCTEEWAQVMGEARLRLEVALPSEETWVSADERLLRRLMVVLLDNARKYT--PESG 376
COG4191 444 SFARKSRDA----AGPVSLREAIEGALELLRGRLRAAGVELELDLPDAPLWVMANEIRLEQVLVNLLQNALDAMagQEDR 519
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 377 YVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGQhkteIHVESTPGAGSTF 456
COG4191 520 RLSIRAQREGGQVVLTVRDNGPGIAPEALPHLFEPFFTTKPVGKGLGLGLAISQNIARDLGGS----LEVANHPEGGASF 595
|
....*...
gi 94967341 457 SFRLARVA 464
COG4191 596 TIELRRAA 603
|
|
|
|
|
|
|
-1 |
| 137934 |
PRK10490 |
PRK10490 |
sensor protein KdpD; Provisional |
sensor protein KdpD; Provisional |
false |
true |
false |
895 |
9e-13 |
70.16 |
28.27 |
11,208,627,3,213,630,3,216,638,27,243,666,21,264,692,21,289,713,18,309,731,3,324,734,4,328,741,12,340,762,93,435,855,25 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 209 QRLppLQT-----NDELQRLSDTLNEMLSRIEAAFTRTRQ-FTADASHELRTPLSLIRTEAE-----LALRKTRTEEEYR 277
PRK10490 628 QRL--LETftllvANALERLTLTASEEQARLASEREQLRNaLLAALSHDLRTPLTVLFGQAEiltldLASEGSPHARQAS 705
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 278 NALGHVLAeserTTELIESLLTLARTDSGAeiIQLvplqtntflrhcTEEW---AQVMGEARLRLE---------VALPS 345
PRK10490 706 EIRQHVLN----TTRLVNNLLDMARIQSGG--FNL------------KKEWltlEEVVGSALQMLEpglsqhpinLSLPE 767
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 346 EETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGG 425
PRK10490 768 PLTLIHVDGPLFERVLINLLENAVKYAGAQAEIGIDAHVEGENLQLDVWDNGPGIPPGQEQLIFDKFARGNKESAVPGVG 847
|
250 260 270
....*....|....*....|....*....|....*
gi 94967341 426 AGLGLSLAkwIAGQHKTEIHVESTPGAGSTFSFRL 460
PRK10490 848 LGLAICRA--IVDVHGGTITAENRPEGGACFRVTL 880
|
|
|
|
|
|
|
-1 |
| 138144 |
PRK10755 |
PRK10755 |
sensor protein BasS/PmrB; Provisional |
sensor protein BasS/PmrB; Provisional |
false |
true |
false |
355 |
1e-12 |
69.71 |
54.37 |
8,217,119,48,266,167,8,279,175,24,303,203,3,306,214,4,312,218,4,325,222,58,384,280,32 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 218 DELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPLSLIRTEAELaLRKTRTEEeyrnaLGHVLAESERTTELIESL 297
PRK10755 120 LEIEAVTSALNQLVSRLTSTLDNERLFTADVAHELRTPLAGVRLHLEL-LAKTHHID-----VAPLIARLDQMMHSVSQL 193
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 298 LTLART----DSG--------AEIIqlVPLQtntflrhctEEWAQVMGEARLRLEVALPSEETWVSADERLLRRLMVVLL 365
PRK10755 194 LQLARAgqsfSSGnyqtvkllEDVI--LPSY---------DELSTMLEQRQQTLLLPESAADITVQGDATLLRLLLRNLV 262
|
170 180 190 200 210
....*....|....*....|....*....|....*....|....*....|.
gi 94967341 366 DNARKYTPESGYVRVFAElTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVD 416
PRK10755 263 ENAHRYSPEGSNITIKLQ-EDGGAVMAVEDEGPGIDESKCGELSKAFVRMD 312
|
|
|
|
|
|
|
-1 |
| 137202 |
PRK09303 |
PRK09303 |
adaptive-response sensory kinase; Validated |
adaptive-response sensory kinase; Validated |
false |
true |
false |
378 |
3e-12 |
68.45 |
69.84 |
10,206,109,12,218,123,9,227,138,5,232,144,4,240,148,16,260,164,7,267,177,32,299,213,83,382,297,51,435,348,25 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 207 LNQRLPPLQTND--ELQRLSDTL------NEMLS-RIEAaftrTRQFTADASHELRTPLslirTEAELAL------RKTR 271
PRK09303 110 LSLRPSESDVGRtqELLQLSDELfvlrqeNETLLeQLKF----KDRLLAMLAHDLRTPL----TAASLAVetlelgQIDP 181
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 272 TEEEYRNALGHVLAESERTTELIESLLT----LARTDSGAEIIQLVPLQTNTFLRHCTEEWAQVMGEARLRLEVALPSEE 347
PRK09303 182 SEELSPALIEQLQDQARRQLEEIERLITdlleVGRTRWEALQFNPQKLDLGSLCQEVILELEKRWLAKSLEIQTDIPSDL 261
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 348 TWVSADERLLRRLMVVLLDNARKYTPESGYVRVFA-ELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGGA 426
PRK09303 262 PSVYADQRRIRQVLLNLLDNAIKYTPEGGTITLTMlHRTTQKVQVSICDTGPGIPEEEQERIFEDRVRLPRDEGTEGYGI 341
|
250 260 270
....*....|....*....|....*....|....
gi 94967341 427 GLGLSLAkwIAGQHKTEIHVESTPGAGSTFSFRL 460
PRK09303 342 GLSVCRR--IVEVHYGQIWVDSEPGQGSCFHFTL 373
|
|
|
|
|
|
|
-1 |
| 137312 |
PRK09470 |
cpxA |
two-component sensor protein; Provisional |
two-component sensor protein; Provisional |
false |
true |
false |
461 |
1e-10 |
62.69 |
41.43 |
6,218,220,57,279,277,29,314,306,7,323,313,13,336,333,39,377,372,39 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 219 ELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPLSLIRTEAELALRKTRTEEEyrnaLGHVLAESERTTELIESLL 298
PRK09470 221 EFRAAGASFNQMVTALERMMSSQQRLLSDISHELRTPLTRLQLATALLRRRQGESKE----LERIETEAQRLDSMINDLL 296
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 299 TLARTDSGAEiiqlvpLQTNTFLrhCTEEWAQVMGEAR-------LRLEVALPSEETWVSADERLLRRLMVVLLDNARKY 371
PRK09470 297 VLSRNQVKNH------LVRETIK--ANSLWSEVLEDAAfeaeqmgKSLTVNQPPGPWPINGNPNALESALENIVRNALRY 368
|
170 180 190 200
....*....|....*....|....*....|....*....|....*
gi 94967341 372 TPESgyVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVD 416
PRK09470 369 SHTK--IEVGFSVDKDGLTITVDDDGPGVPEEEREQIFRPFYRVD 411
|
|
|
|
|
|
|
-1 |
| 132001 |
TIGR02956 |
TMAO_torS |
TMAO reductase sytem sensor TorS |
TMAO reductase sytem sensor TorS |
false |
true |
false |
968 |
2e-10 |
62.10 |
30.99 |
12,189,381,14,203,401,28,231,430,3,234,434,8,242,465,23,266,488,56,322,547,13,336,560,14,351,574,23,374,598,10,385,608,31,418,639,42 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 190 RSVDEITAMARSIH------ERNLNQRLPPLQTNDELQRLSDTLNEML-SRI-EAAFTRTR------------------- 242
TIGR02956 382 RGDDELAHMGRAIEafrdtaAHNLKLQADERQVAQELQEHKESLEQLVaQRTqELAETNERlnaevknhakaraeaeean 461
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 243 ----QFTADASHELRTPLSLIRTEAELaLRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTN 318
TIGR02956 462 raksAFLATMSHEIRTPLNGILGTLEL-LGDTGLTSQQQQYLQVINRSGESLLDILNDILDYSKIEAGHLSISPRPFDLN 540
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 319 TFLR---HCTEEWAQVMGEArLRLEVALPSEETWVsADERLLRRLMVVLLDNARKYTPE-SGYVRVFAELtDREVTVGVQ 394
TIGR02956 541 ALLDdvhHLMVSRAQLKGIQ-LRLNIPEQLPNWWQ-GDGPRIRQVLINLVGNAIKFTDRgSVVLRVSLND-DSSLLFEVE 617
|
250 260 270 280 290 300
....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 94967341 395 DNGCGIQAEHLPRIFDRFYRVDkaRSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRL 460
TIGR02956 618 DTGCGIAEEEQATLFDAFTQAD--GRRRSGGTGLGLAISQRLVEAMDGELGVESELGVGSCFWFTL 681
|
|
|
|
|
|
|
-1 |
| 137849 |
PRK10364 |
PRK10364 |
sensor protein ZraS; Provisional |
sensor protein ZraS; Provisional |
false |
true |
false |
455 |
5e-10 |
61.10 |
45.05 |
5,245,242,30,276,272,9,285,282,20,309,302,120,435,422,25 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 246 ADASHELRTPLSLIRTEAELALRKTRTEEEyRNALGHVLA-ESERTTELIESLLTLARTDSgaeiIQLVPLQTNTFLRHC 324
PRK10364 243 AGVAHEIRNPLSSIKGLAKYFAERAPAGGE-AHQLAQVMAkEADRLNRVVSELLELVKPTH----LALQAVDLNTLINHS 317
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 325 TEEWAQVMGEARLRLEVALPSEETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEH 404
PRK10364 318 LQLVSQDANSREIQLRFTANDTLPEIQADPDRLTQVLLNLYLNAIQAIGQHGVISVTASESGAGVKISVTDSGKGIAADQ 397
|
170 180 190 200 210
....*....|....*....|....*....|....*....|....*....|....*.
gi 94967341 405 LPRIFDRFYRVDKARSRGEGGAGLGlslakwIAGQHKTEIHVESTPGAGSTFSFRL 460
PRK10364 398 LEAIFTPYFTTKAEGTGLGLAVVHN------IVEQHGGTIQVASQEGKGATFTLWL 447
|
|
|
|
|
|
|
-1 |
| 137309 |
PRK09467 |
envZ |
osmolarity sensor protein; Provisional |
osmolarity sensor protein; Provisional |
false |
true |
false |
437 |
2e-08 |
55.69 |
54.00 |
9,164,156,14,179,170,33,213,203,47,264,250,12,283,262,4,287,271,20,310,291,12,326,303,46,374,349,43 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 165 VFLFLVPCFVLIAAvGSYYFSRRALRSVDEITAMARSIHERNLNQRLPpLQTNDELQRLSDTLNEMLSRIEAAFTRTRQF 244
PRK09467 157 LFRYLLVIGLLSVA-GGWLFIRIQNRPLVALEHAALQVGKGEIPPPLP-EYGASEVRSVTRAFNQMSAGIKQLEDDRALL 234
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 245 TADASHELRTPLSLIRteaeLALRKTRTEEEYrnalghvLAES-----ERTTELIESLLTLARTDSGAeiiQLVPLQTNT 319
PRK09467 235 MAGVSHDLRTPLTRIR----LATEMMSEEDGY-------LAESinkdiEECNAIIEQFIDYLRTDQEM---PMEMADLNA 300
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 320 FLRhcteEWAQVMGEARLRLEVALPSEETWVSADERLLRRLMVVLLDNARKYTpeSGYVRVFAELTDREVTVGVQDNGCG 399
PRK09467 301 LLG----EVIAAESGYEREIETALYPGPIEVPMNPIAIKRALANLVVNAARYG--NGWIKVSSGTEGNRAWFQVEDNGPG 374
|
250
....*....|....*...
gi 94967341 400 IQAEHLPRIFDRFYRVDK 417
PRK09467 375 IPEEQIKHLFQPFTRGDS 392
|
|
|
|
|
|
|
-1 |
| 138397 |
PRK11091 |
PRK11091 |
aerobic respiration control sensor protein ArcB; Provisional |
aerobic respiration control sensor protein ArcB; Provisional |
false |
true |
false |
779 |
9e-08 |
53.46 |
31.19 |
13,243,285,22,266,307,15,281,324,6,287,345,6,295,351,21,328,372,5,334,377,13,348,390,29,377,420,10,388,430,27,415,458,41,456,501,16,472,523,5 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 244 FTADASHELRTPLSLIRTEAELaLRKTRTEEEYRNALG--HVLAES---------------ERTTELieSLLTLARTDSG 306
PRK11091 286 FISTISHELRTPLNGIVGLSRM-LLDTELTAEQEKYLKtiHVSAITlgnifndiidmdkmdRRKLQL--DNQPVDFTDFL 362
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 307 AEIIQLVPLQtntflrhcteewAQVMGeARLRLEVALPSEEtWVSADERLLRRLMVVLLDNARKYTPESGY-VRVFAELT 385
PRK11091 363 ADLENLSGLQ------------AEQKG-LRFDLEPLLPLPH-KVITDGTRLRQILWNLISNAVKFTQQGQVtVRVRYEDG 428
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 386 DReVTVGVQDNGCGIQAEHLPRIFDRFYRV-DKARSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTF--SFRLAR 462
PRK11091 429 DM-LHFEVEDSGIGIPEDELDKIFAMYYQVkDSHGGKPATGTGIGLAVSRRLAQNMGGDITVTSEEGKGSTFtlTIHAPA 507
|
250 260
....*....|....*....|.
gi 94967341 463 VANNTANSAS------PSLDI 477
PRK11091 508 VAEEVEDAFDeddmplPALNI 528
|
|
|
|
|
|
|
-1 |
| 138194 |
PRK10815 |
PRK10815 |
sensor protein PhoQ; Provisional |
sensor protein PhoQ; Provisional |
false |
true |
false |
484 |
6e-07 |
50.86 |
45.66 |
9,190,214,20,210,236,3,214,239,47,265,286,9,274,296,33,307,334,8,320,342,30,351,372,23,376,395,40 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 191 SVDEITAMARSIHERNLNQR--LPPlQTNDELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPLSLIRTeaelALR 268
PRK10815 215 SLRPIEALAKEVRELEEHNReqLNP-NTTRELTSLVRNLNRLLKSERERYDKYRTTLTDLTHSLKTPLAVLQS----TLR 289
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 269 KTRTEE-EYRNALGHVLAESERTTELIESLLTLARTDSGA-----EIIQLVPLqtntfLRHCTEEWAQVMGEARLRLEVA 342
PRK10815 290 SLRTEKmSVSDAEPVMLEQISRISQQIGYYLHRASMRGEGtllsrELHPVAPL-----LDNLTSALNKVYQRKGVNISLD 364
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....
gi 94967341 343 LPSEETWVsADERLLRRLMVVLLDNARKYTPEsgYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDRFYRVD 416
PRK10815 365 ISPEISFV-GEQNDFMEVMGNVLDNACKYCLE--FVEISARQTDEHLHIVVEDDGPGIPESKRELIFDRGQRVD 435
|
|
|
|
|
|
|
-1 |
| 137612 |
PRK09959 |
PRK09959 |
hybrid sensory histidine kinase in two-component regulatory system with EvgA; Provisional |
hybrid sensory histidine kinase in two-component regulatory system with EvgA; Provisional |
false |
true |
false |
1197 |
2e-06 |
48.96 |
18.46 |
5,242,713,107,349,821,25,375,846,13,388,864,29,419,893,41 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 243 QFTADASHELRTPLSLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLARTDSGAEIIQLVPLQTNTFLR 322
PRK09959 714 QFLATMSHEIRTPISSIMGFLELLSGSGLSKEQRVEAISLAYATGQSLLGLIGEILDVDKIESGNYQLQPQWVDIPTLVQ 793
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 323 HCTEEWAQVMGEARLRLEVALPSEETW-VSADERLLRRLMVVLLDNARKYTPEsGYVRVFAELTDRE-----VTVGVQDN 396
PRK09959 794 NTCHSFGAIAASKSIALSCSSTFPEHYlVKIDPQAFKQVLSNLLSNALKFTTE-GAVKITTSLGHIDdnhavIKMTIMDS 872
|
170 180 190 200 210 220
....*....|....*....|....*....|....*....|....*....|....*....|....
gi 94967341 397 GCGIQAEHLPRIFDRFYRVDKarSRGEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRL 460
PRK09959 873 GSGLSQEEQQQLFKRYSQTSA--GRQQTGSGLGLMICKELIKNMQGDLSLESHPGIGTTFTITI 934
|
|
|
|
|
|
|
-1 |
| 131962 |
TIGR02916 |
PEP_his_kin |
putative PEP-CTERM system histidine kinase |
putative PEP-CTERM system histidine kinase |
false |
true |
false |
679 |
2e-05 |
45.87 |
37.26 |
12,194,425,14,213,439,23,236,464,8,244,478,9,253,490,11,268,501,9,277,511,22,300,533,15,324,548,24,349,572,56,405,629,7,418,636,42 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 195 ITAMARSIHERNLNqrlppLQTNDELQRLSDTLNEMLSRIEA--AFTRTRQF------TADASHELR---TPLSLIRTEA 263
TIGR02916 426 FVVLARPRTAGEFN-----WEVRDLLKTAGRQAASYLAQMEAseALAEARQFeafnrmSAFVVHDLKnlvAQLSLLLRNA 500
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 264 ElalrKTRTEEEYR-NALGHVLAESERTTELIESLLTlARTDSGAEIIQLVPLqtntflrhcTEEWAQVMGEARLRLEVA 342
TIGR02916 501 E----RHKDNPEFQdDMLETVENAVNRMKKLLAQLRS-KGLEEEKLCVDLVDL---------LRRAIASKRAQGPRPEVS 566
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 343 LPSEETwVSADERLLRRLMVVLLDNARKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHL-PRIFDRFyrvdkaRSR 421
TIGR02916 567 IDTDLS-VRADRERLERVLGHLVQNALEATPGEGRVAIRVERECGAARIEIEDSGCGMSPAFIrERLFKPF------DTT 639
|
250 260 270
....*....|....*....|....*....|....*....
gi 94967341 422 GEGGAGLGLSLAKWIAGQHKTEIHVESTPGAGSTFSFRL 460
TIGR02916 640 KGAGMGIGVYECRQYVEEIGGRIEVESTPGQGTIFTLVL 678
|
|
|
|
|
|
|
-1 |
| 34605 |
COG5000 |
NtrY |
Signal transduction histidine kinase involved in nitrogen fixation and metabolism regulation [Signal transduction mechanisms] |
Signal transduction histidine kinase involved in nitrogen fixation and metabolism... |
false |
true |
false |
712 |
3e-05 |
45.33 |
23.60 |
5,248,493,25,273,523,32,309,555,17,328,572,40,368,619,42 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 249 SHELRTPLSLIRTEAELALRKTRTE-----EEYRNALGHVLAESERTTELIESLLTLARTDSgaeiIQLVPLQTNTFLRH 323
COG5000 494 AHEIKNPLTPIQLSAERLLRKLGKEidedrEVFDRCTDTIIRQVEDIKRMVDEFRAFARMPA----PKLEKSDLRALLKE 569
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 324 CTEewAQVMGEARLRLEVALPSEETWVSADERLLRRLMVVLLDNA-------RKYTPESGYVRVFAELTDREVTVGVQDN 396
COG5000 570 VSF--LYEIGNDHIVFAAEFGGEPLIGMADATLLGQVFGNLLKNAaeaieavEAEERRTALIRVSLDDADGRIVVDVIDN 647
|
170
....*....|....
gi 94967341 397 GCGIQAEHLPRIFD 410
COG5000 648 GKGFPRENRHRALE 661
|
|
|
|
|
|
|
-1 |
| 139897 |
PRK13837 |
PRK13837 |
two-component VirA-like sensor kinase; Provisional |
two-component VirA-like sensor kinase; Provisional |
false |
true |
false |
831 |
1e-04 |
43.53 |
26.96 |
7,232,448,7,243,455,59,304,514,13,330,527,15,345,552,41,386,608,27,419,635,37 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 233 RIEAAFTrtrqFTADASHELRTPLSLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLARtdSGAEIIQL 312
PRK13837 449 RLEAVGT----LASGIAHNFNNILGAILGYAEMALNKLRRHSRARRHIDEIISSGDRARLIIDQILTFGR--KGERRTKP 522
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 313 VPLQTntflrhcteewaqVMGEARLRLEVALPS----------EETWVSADERLLRRLMVVLLDNARKYTPESGYVRVFA 382
PRK13837 523 FSLSE-------------LVTEIAPLLRVSLPPtveldfdfdqEPAVVEGNPAQLQQVILNLCKNAAQAMDENGRVDIRL 589
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 383 ELTD---------------REVTVGVQDNGCGIQAEHLPRIFDRFYrvdkarSRGEGGAGLGLSLAKWIAGQHKTEIHVE 447
PRK13837 590 SRVDlrkpkvlahgtappgRYVLLRVSDTGRGIDEAVLPHIFEPFF------TTRARGTGLGLATVHGIVSAHAGYIDVQ 663
|
....*....
gi 94967341 448 STPGAGSTF 456
PRK13837 664 STVGRGTRF 672
|
|
|
|
|
|
|
-1 |
| 138589 |
PRK11466 |
PRK11466 |
hybrid sensory histidine kinase TorS; Provisional |
hybrid sensory histidine kinase TorS; Provisional |
false |
true |
false |
912 |
1e-04 |
43.09 |
26.21 |
7,218,421,47,266,468,47,313,517,33,346,551,32,378,584,5,385,589,53,442,642,18 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 219 ELQRLSDTLNEMLSRIEAAFTRTRQFTADASHELRTPLSLIRTEAELaLRKTRTEEEYRNALGHVLAESERTTELIESLL 298
PRK11466 422 ELQELVIEHRQARAEAEKASQAKSAFLAAMSHEIRTPLYGILGTAQL-LADNPALNAQRDDLRAITDSGESLLTILNDIL 500
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 299 TLARTDSGAEIIQLV--PLQTNTFLRHCTEEWAQVMGEARLRLEVALPSE-ETWVSADERLLRRLMVVLLDNARKYTPES 375
PRK11466 501 DYSAIEAGGKNVSVSdePFEPRPLLESTLQLMSGRVKGRPIRLATDIADDvPSALMGDPRRIRQVITNLLSNALRFTDEG 580
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 376 GYV-RVFAEltDREVTVGVQDNGCGIQAEHLPRIFDRFYRVDKARSRGEGGAGLGLSLAKWIAGqhktEIHVESTPGAGS 454
PRK11466 581 SIVlRSRTD--GEQWLVEVEDSGCGIDPAKLAEIFQPFVQVSGKRGGTGLGLTISSRLAQAMGG----ELSATSTPEVGS 654
|
....*.
gi 94967341 455 TFSFRL 460
PRK11466 655 CFCLRL 660
|
|
|
|
|
|
|
-1 |
| 138539 |
PRK11360 |
PRK11360 |
sensory histidine kinase AtoS; Provisional |
sensory histidine kinase AtoS; Provisional |
false |
true |
false |
607 |
0.001 |
40.06 |
14.17 |
3,145,170,57,203,227,11,216,238,18 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 146 IEAGASTNGIHHTLEQLRNVFLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIhERNLNQRLPPLqtNDELQRLSD 225
PRK11360 171 IWANELTEDIRRQAWKMDVRIYIVLTAGLVIGLLLIVLLSRRLSANVDIITDGLSTL-EQDLPTRLPPL--PGELGQISQ 247
|
....*....
gi 94967341 226 TLNEMLSRI 234
PRK11360 248 AINNLAQAL 256
|
|
|
|
|
|
|
-1 |
| 33640 |
COG3850 |
NarQ |
Signal transduction histidine kinase, nitrate/nitrite-specific [Signal transduction mechanisms] |
Signal transduction histidine kinase, nitrate/nitrite-specific [Signal transduction... |
false |
true |
false |
574 |
0.004 |
38.34 |
16.72 |
2,156,143,54,211,197,42 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 157 HTLEQLRNVFLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIHERNLNQRlPPLQTNDELQRLSDTLNEMLSRIEA 236
COG3850 144 RKTILLVLVQLAGMLLILLLVVFTIYWLRRRVVRPLNQLTSAAQRIGRRQFDQR-PTDTGRNELGLLGRAFNQMSGELKK 222
|
90
....*....|....*..
gi 94967341 237 AFTRTRQFTADASHELR 253
COG3850 223 LYADLEQRVEEKTRDLE 239
|
|
|
|
|
|
|
-1 |
| 34605 |
COG5000 |
NtrY |
Signal transduction histidine kinase involved in nitrogen fixation and metabolism regulation [Signal transduction mechanisms] |
Signal transduction histidine kinase involved in nitrogen fixation and metabolism... |
false |
true |
false |
712 |
0.004 |
38.40 |
13.34 |
2,165,282,65,230,350,27 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 166 FLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIHERNLNQRLPPLQTNDELQRLSDTLNEM---LSRIEAAFTRTR 242
COG5000 283 YLSTALLVLLAAIWTAIAFARRIVRPIRKLIEAADEVADGDLDVQVPVRRVDEDVGRLSKAFNKMteqLSSQQEALERAK 362
|
90
....*....|....*
gi 94967341 243 QFTADASHELRTPLS 257
COG5000 363 DALEQRRRFLEAVLS 377
|
|
|
|
|
|
|
-1 |
| 32791 |
COG2972 |
COG2972 |
Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms] |
Predicted signal transduction protein with a C-terminal ATPase domain [Signal... |
false |
true |
false |
456 |
0.004 |
38.16 |
57.02 |
10,134,149,69,213,218,30,255,248,18,280,266,7,293,273,20,314,293,8,322,304,15,337,333,11,350,344,18,368,366,43 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 135 KAVSVQDRLYTIEAGASTNGIHHTLEQLRNVFLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIHernlnqrlppL 214
COG2972 150 SFIIFRKTEWLVYLVVPKLSILLSLIRLLFILVILVLLFLVVILLLSSFSSRSILLPILGLILLLSRIA----------L 219
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 215 QTNDELQRLSDTLNEMLSRIEAAFTRTRQftadashelrtpLSLIRTEAELALRKTRTEeeyrnalGHVLAESerttelI 294
COG2972 220 GYLSELKEISETINEMEERLEYLIEENYS------------LEQEQLEAELRALQSQIN-------PHFLYNT------L 274
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 295 ESLLTLARTDSGAEIIQLVpLQTNTFLR---HCTEEWAQVMGEARL--------------RLEVALPSEETwvSADERLL 357
COG2972 275 ETIRMLAEEDDPEEAAKVV-KALSKLLRyslSNLDNIVTLEIELLLiekyleiqklrigdRLEVPLPIDEE--LEPLIDP 351
|
250 260 270 280 290
....*....|....*....|....*....|....*....|....*....|....*...
gi 94967341 358 RRLMVVLLDNA----RKYTPESGYVRVFAELTDREVTVGVQDNGCGIQAEHLPRIFDR 411
COG2972 352 KLVLQPLVENAiehgIEPKRPGGSIAISAKKQDDVIQISISDNGPGIDEEKLEGLSTK 409
|
|
|
|
|
|
|
-1 |
| 31182 |
COG0840 |
Tar |
Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms] |
Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction... |
false |
true |
false |
408 |
0.004 |
38.04 |
37.25 |
2,149,45,63,213,108,89 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 150 ASTNGIHHTLEQLRNVFLFLVPCFVLIAAVGSYYFSRRALRSVDEITAMARSIHERNLNQRLPpLQTNDELQRLSDTLNE 229
COG0840 46 DAASAEAAALKAVLKFLLISLLVAIIVVLVLAILLLRAILEPISDLLEVVERIAAGDLTKRID-ESSNDEFGQLAKSFNE 124
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|...
gi 94967341 230 MLSRIEAAFTRTRQFTADASHELRTPLSLIRTEAELALRKTRTEEEYRNALGHVLAESERTTELIESLLTLAR 302
COG0840 125 MILNLRQIIDAVQDNAEALSGASEEIAASATELSARADQQAESLEEVASAIEELSETVKEVAFNAKEAAALAS 197
|
|
|
|
|
|
|
-1 |
| 139663 |
PRK13557 |
PRK13557 |
histidine kinase; Provisional |
histidine kinase; Provisional |
false |
true |
false |
538 |
0.009 |
37.01 |
27.32 |
6,276,200,29,309,229,26,336,255,7,344,262,7,351,270,32,383,317,30 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 94967341 277 RNALGHVLAESERTTELIESLLTLARTDSgaeiIQLVPLQTNTFLRHCTEEWAQVMGEArLRLEVALpSEETWVS-ADER 355
PRK13557 201 ARSVEHIRAAAERAATLTQQLLAFARKQK----LDGRVVNLNGLVSGMGEMAERTLGDA-VTIETDL-APDLWNCrIDPT 274
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|...
gi 94967341 356 LLRRLMVVLLDNARKYTPESGYVRVFAE---------------LTDREVTVGVQDNGCGIQAEHLPRIFDRFY 413
PRK13557 275 QAEVALLNVLINARDAMPEGGRVTVRTEnveitehdlamyhqlPPGRYVSIAVTDTGSGMPPEILARVMEPFF 347
|
|
|
|
|
|
|
-1 |
|