| 30163 |
cd01948 |
EAL |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria. |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called... |
true |
false |
true |
240 |
2e-64 |
242.43 |
98.75 |
1,287,0,237 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 288 AELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYVLDAALASAVHWRQK 367
cd01948 1 ADLRRALERGEFELYYQPIVDLRTGRIVGYEALLRWRHPEGGLISPAEFIPLAEETGLIVELGRWVLEEACRQLARWQAG 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 368 GIALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRDLGVRLSCDDFGTGTTPL 447
cd01948 81 GPDLRLSVNLSARQLRDPDFLDRLLELLAETGLPPRRLVLEITESALIDDLEEALATLRRLRALGVRIALDDFGTGYSSL 160
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*..
gi 117928031 448 PRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPPVP 524
cd01948 161 SYLKRLPVDYLKIDRSFVRDIETDPEDRAIVRAIIALAHSLGLKVVAEGVETEEQLELLRELGCDYVQGYLFSRPLP 237
|
|
cl00290 |
140582 |
EAL |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria. |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called... |
-1 |
| 133472 |
cd01949 |
GGDEF |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as domain of unknown function 1 (DUF1). It is widely present in bacteria and often links to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain has been suggested to be homologous to the adenylyl cyclase catalytic domain. This prediction correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesiveness in bacteria. |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue... |
true |
false |
true |
157 |
3e-31 |
131.94 |
96.82 |
2,112,0,90,203,90,62 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 113 RDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLGAD 192
cd01949 1 TDPLTGLPNRRAFEERLERLLARARRSGRPLALLLIDLDHFKQINDTYGHAAGDEVLKEVARRLRSSLRESDLVARLGGD 80
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|...
gi 117928031 193 EFAVLLRDFNrPEGADAMSRAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHAR 265
cd01949 81 EFAILLPGTD-LEEAEELAERLRKAIEEPFFIDGEEIRVTASIGIAEYPEDGEDLEELLRRADKALYQAKRSG 152
|
|
cl00291 |
140583 |
GGDEF |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as domain of unknown function 1 (DUF1). It is widely present in bacteria and often links to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain has been suggested to be homologous to the adenylyl cyclase catalytic domain. This prediction correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesiveness in bacteria. |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue... |
0 |
| 128367 |
smart00052 |
EAL |
Putative diguanylate phosphodiesterase |
Putative diguanylate phosphodiesterase |
false |
false |
false |
241 |
5e-64 |
240.58 |
97.93 |
1,288,2,236 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 289 ELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYVLDAALASAVHWRQKG 368
smart00052 3 ELRQALENGQFLLYYQPIVSLRTGRLVGVEALIRWQHPEGGIISPDEFIPLAEETGLIVPLGRWVLEQACQQLAEWQAQG 82
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 369 IALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRDLGVRLSCDDFGTGTTPLP 448
smart00052 83 PPLRISINLSARQLISPDLVPRVLELLEETGLPPQRLELEITESVLLDDDESAVATLQRLRELGVRIALDDFGTGYSSLS 162
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 117928031 449 RLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPPVP 524
smart00052 163 YLKRLPVDLLKIDKSFVRDLQTDPEDEAIVQSIIELAQKLGLQVVAEGVETPEQLDLLRSLGCDYGQGYLFSRPLP 238
|
|
cl00290 |
140582 |
EAL |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria. |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called... |
-1 |
| 32382 |
COG2200 |
Rtn |
c-di-GMP phosphodiesterase class I (EAL domain) [Signal transduction mechanisms] |
c-di-GMP phosphodiesterase class I (EAL domain) [Signal transduction mechanisms] |
false |
false |
false |
256 |
9e-59 |
223.28 |
100.00 |
2,282,0,86,369,86,170 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 283 RLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYVLDAALASAV 362
COG2200 1 RLQLERDLRQALENGEFSLYYQPIVDLATGRIVGYEALLRWRHPDGGLISPGEFIPLAEETGLIVELGRWVLEEACRQLR 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 363 HWRQKGiALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRDLGVRLSCDDFGT 442
COG2200 81 TWPRAG-PLRLAVNLSPVQLRSPGLVDLLLRLLARLGLPPHRLVLEITESALIDDLDTALALLRQLRELGVRIALDDFGT 159
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 443 GTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPP 522
COG2200 160 GYSSLSYLKRLPPDILKIDRSFVRDLETDARDQAIVRAIVALAHKLGLTVVAEGVETEEQLDLLRELGCDYLQGYLFSRP 239
|
250
....*....|....*..
gi 117928031 523 VPGALIGDVLRPDGERA 539
COG2200 240 LPADALDALLSSSQSRV 256
|
|
cl00290 |
140582 |
EAL |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria. |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called... |
-1 |
| 109613 |
pfam00563 |
EAL |
EAL domain |
EAL domain |
false |
false |
false |
236 |
3e-53 |
204.96 |
100.00 |
5,286,0,83,369,86,27,397,113,27,425,140,43,469,183,53 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 287 HAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYVLDAALASAVHWRQ 366
pfam00563 1 EQALREALENGEFSLYFQPIVDLRTGKVLGYEALLRWQHPDGGLIPPDEFLPLAERLGLIAELDRWVLEKALAQLAEWRG 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 367 KGI---ALPVSVNISARDLHDPSFPDRVDTLLHlHGVPADRLTLEITETTLNSRLYPADAVaKKLRDLGVRLSCDDFGTG 443
pfam00563 81 NALlppDLPLSVNLSPASLLDPSFLEALLALKQ-GGLPPSRLVLEITESDLDEDLRLLEAL-ARLRSLGFRLALDDFGTG 158
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 117928031 444 TTPLPRLRDLPLAELKIDNTLIAGIvGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPP 522
pfam00563 159 YSSLSYLSRLPPDYIKIDRSFIKDL-SDPESRALLRALIALARELGIKVVAEGVETEEQLELLKELGIDYVQGYLFSKP 236
|
|
cl00290 |
140582 |
EAL |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria. |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called... |
-1 |
| 110022 |
pfam00990 |
GGDEF |
GGDEF domain |
GGDEF domain |
false |
false |
false |
160 |
5e-28 |
120.81 |
97.50 |
2,110,0,103,213,105,51 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 111 AGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLG 190
pfam00990 1 AAHDPLTGLPNRRYFEEELEQELQRAQRRQSPLALLLLDLDNFKRINDTYGHAVGDEVLQEVAQRLSSSLRRSDLVARLG 80
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 117928031 191 ADEFAVLLRDFNRPEGADAMSRA--ILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHA 264
pfam00990 81 GDEFAILLPDTSLEGAQELAERIrrLLAALKIPHTLSGLPLYVTISIGIAAYPNDGEDAEDLLKRADQALYQAKNQ 156
|
|
cl00291 |
140583 |
GGDEF |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as domain of unknown function 1 (DUF1). It is widely present in bacteria and often links to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain has been suggested to be homologous to the adenylyl cyclase catalytic domain. This prediction correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesiveness in bacteria. |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue... |
-1 |
| 128563 |
smart00267 |
GGDEF |
diguanylate cyclase |
diguanylate cyclase |
false |
false |
false |
163 |
1e-26 |
116.58 |
95.09 |
2,108,0,94,203,94,61 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 109 EHAGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVAR 188
smart00267 1 RLAFRDPLTGLPNRRYFEEELEQELQRAQRQGSPFALLLIDLDNFKDINDTYGHAVGDELLQEVAQRLSSCLRPGDLLAR 80
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 117928031 189 LGADEFAVLLRDFNrPEGADAMSRAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHA 264
smart00267 81 LGGDEFALLLPETS-LEEAIALAERILQQLREPIIIHGIPLYLTISIGVAAYPNPGEDAEDLLKRADTALYQAKKA 155
|
|
cl00291 |
140583 |
GGDEF |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as domain of unknown function 1 (DUF1). It is widely present in bacteria and often links to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain has been suggested to be homologous to the adenylyl cyclase catalytic domain. This prediction correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesiveness in bacteria. |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue... |
-1 |
| 32381 |
COG2199 |
COG2199 |
c-di-GMP synthetase (diguanylate cyclase, GGDEF domain) [Signal transduction mechanisms] |
c-di-GMP synthetase (diguanylate cyclase, GGDEF domain) [Signal transduction... |
false |
false |
false |
181 |
3e-25 |
111.75 |
90.06 |
3,101,10,99,201,109,48,249,158,15 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 102 ATHRRASEHAGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVR 181
COG2199 11 KAEERLERLALHDPLTGLPNRRAFEERLERALARARRHGEPLALLLLDLDHFKQINDTYGHAAGDEVLREVARRLRSNLR 90
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 182 HRDVVARLGADEFAVLLRDfNRPEGADAMSRAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAE-LLRRAMVALQA 260
COG2199 91 EGDLVARLGGDEFAVLLPG-TSLEEAARLAERIRAALEEPFFLGGEELRVTVSIGVALYPEDGSDDAElLLRRADLALYR 169
|
....
gi 117928031 261 ARHA 264
COG2199 170 AKRA 173
|
|
cl00291 |
140583 |
GGDEF |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as domain of unknown function 1 (DUF1). It is widely present in bacteria and often links to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain has been suggested to be homologous to the adenylyl cyclase catalytic domain. This prediction correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesiveness in bacteria. |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue... |
-1 |
| 129356 |
TIGR00254 |
GGDEF |
diguanylate cyclase (GGDEF) domain |
diguanylate cyclase (GGDEF) domain |
false |
false |
false |
165 |
1e-19 |
93.55 |
93.94 |
2,110,1,118,228,120,36 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 111 AGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLG 190
TIGR00254 2 AVRDPLTGLYNRRYLEEMLDSELKRARRFQRSFSVLMIDIDNFKKINDTLGHDVGDEVLREVARILQSSVRGSDVVGRYG 81
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 117928031 191 ADEFAVLLRDFNRPEGADAMSRAILRALREPFDVAGLP-LTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHA 264
TIGR00254 82 GEEFVVILPGTPLEDALSKAERLRDAINSKPIEVAGSEtLTVTVSIGVACYPGHGLTLEELLKRADEALYQAKKA 156
|
|
cl00291 |
140583 |
GGDEF |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as domain of unknown function 1 (DUF1). It is widely present in bacteria and often links to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain has been suggested to be homologous to the adenylyl cyclase catalytic domain. This prediction correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesiveness in bacteria. |
Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue... |
-1 |
| 138661 |
PRK11596 |
PRK11596 |
EAL domain-containing protein; Provisional |
EAL domain-containing protein; Provisional |
false |
false |
false |
255 |
0.003 |
38.92 |
35.69 |
1,433,153,91 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 434 RLSCDDFGTGTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTT 513
PRK11596 154 PLWLDDFGTGMANFSALSEVRYDYIKVARELFVMLRQSPEGRTLFSQLLHLMNRYCRGVIVEGVETPEEWRDVQRSPAFA 233
|
90
....*....|.
gi 117928031 514 GQGYYFSPPVP 524
PRK11596 234 AQGYFLSRPAP 244
|
|
cl00290 |
140582 |
EAL |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria. |
EAL domain. This domain is found in diverse bacterial signaling proteins. It is called... |
-1 |
| 34606 |
COG5001 |
COG5001 |
Predicted signal transduction protein containing a membrane domain, an EAL and a GGDEF domain [Signal transduction mechanisms] |
Predicted signal transduction protein containing a membrane domain, an EAL and a GGDEF... |
false |
true |
false |
663 |
6e-67 |
250.33 |
61.99 |
2,110,227,256,369,483,155 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 111 AGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLG 190
COG5001 228 ANLDSLTGLPNRRRFFAELDARLAAARQSGRRLVLGVIDLDGFKPVNDAFGHATGDRLLIEVGRRLKAFDGAPILAARLG 307
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 191 ADEFAVLLRDFNRPEGADAMSRAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHARSPAVE 270
COG5001 308 GDEFALIIPALEDDALRVAGARALCESLQAPYDLRGVRVQVGASIGIAPFPSGADTSEQLFERADYALYHAKQNGKGAAV 387
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 271 NYRPAHDPAGAERLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVT 350
COG5001 388 LFDARHEAAIRDMAVVEQALRSADLEQELSVHFQPIVDIVSGKTIALEALARWHSPEIGPVPPDVFIGIAERSGQIVELT 467
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 351 SYVLDAALASAVHWRQkgiALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRD 430
COG5001 468 RLLLAKALREARAWPM---DVRVSINLSARDLASMENVRRLLAIVSESCIAPHRLDFEITETAIVCDFDQARDALAALHE 544
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 431 LGVRLSCDDFGTGTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLG 510
COG5001 545 LGVRTALDDFGTGYSSLSHLRALPLDKIKIDRSFVSDLEENPTSEDIVRTVLQLGRNLRMECVVEGVETEAQRDRVAALG 624
|
410
....*....|....
gi 117928031 511 CTTGQGYYFSPPVP 524
COG5001 625 ATVMQGYHYARPMP 638
|
|
|
|
|
|
|
-1 |
| 137662 |
PRK10060 |
PRK10060 |
RNase II stability modulator; Provisional |
RNase II stability modulator; Provisional |
false |
true |
false |
663 |
3e-62 |
234.62 |
64.71 |
6,98,219,5,103,225,7,110,236,25,137,261,68,206,329,103,310,432,216 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 99 GTTAT-HRRASEH----AGRDDLTGVANRPALLAALDDTFEDihRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIA 173
PRK10060 220 GTDITeERRAQERlrilANTDSITGLPNRNAIQELIDHAIAQ--ADNNQVGIVYLDLDNFKKVNDAYGHMFGDQLLQDVS 297
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 174 MRLASRVRHRDVVARLGADEFAVLLRDFNRPEgADAMSRAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRR 253
PRK10060 298 LAILSCLEEDQTLARLGGDEFLVLASHTSQAA-LEAMASRILTRLRLPFRIGLIEVYTGCSIGIALSPEHGDDSESLIRS 376
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 254 AMVALQAARHARSPAVENYRPAHDPAGAERLTLHAELDAALRTGQLVLHYQSTVDLaTGRTVGVEALLRWQHPRRGLLRP 333
PRK10060 377 ADTAMYTAKEGGRGQFCVFSPEMNQRVFEYLWLDTNLRKALENDQLVIHYQPKITW-RGEVRSLEALVRWQSPERGLIPP 455
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 334 AEFLPAAEQSELIGLVTSYVLDAALASAVHWRQKGIALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETT 413
PRK10060 456 LEFISYAEESGLIVPLGRWVILDVVRQAAKWRDKGINLRVAVNVSARQLADQTIFTALKQVLQELNFEYCPIDVELTESC 535
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 414 LNSRLYPADAVAKKLRDLGVRLSCDDFGTGTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVV 493
PRK10060 536 LIENEELALSVIQQFSQLGAQVHLDDFGTGYSSLSQLARFPIDAIKLDQSFVRDIHKQPVSQSLVRAIVAVAQALNLQVI 615
|
410 420 430
....*....|....*....|....*....|...
gi 117928031 494 AEGIERQDEREVLIRLGCTTGQGYYFSPPVPGA 526
PRK10060 616 AEGVETAKEDAFLTKNGVNERQGFLFAKPMPAV 648
|
|
|
|
|
|
|
-1 |
| 138538 |
PRK11359 |
PRK11359 |
cAMP phosphodiesterase; Provisional |
cAMP phosphodiesterase; Provisional |
false |
true |
false |
799 |
5e-57 |
217.40 |
51.94 |
6,113,378,29,146,407,54,201,461,38,239,500,7,249,507,123,372,631,162 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 114 DDLTGVANRPALLAALDDTFEDIHRRAAYagllVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLGADE 193
PRK11359 379 DPMTGLPNRNNLHNYLDDLVDKAVSPVVY----LIGVDHIQDVIDSLGYAWADQALLEVVNRFREKLKPDQYLCRIEGTQ 454
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 194 FAVLLRDfNRPEGADAMSRAILRALREPFDVAGLPLTLDVAAGLAV-APRDADTsaeLLRRAMVALQAARHARSPAVENY 272
PRK11359 455 FVLVSLE-NDVSNITQIADELRNVVSKPIMIDDKPFPLTLSIGISYdVGKNRDY---LLSTAHNAMDYIRKNGGNGWQFF 530
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 273 RPAHDPAGAERLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSY 352
PRK11359 531 SPAMNEMVKERLVLGAALKEAISNNQLKLVYQPQIFAETGELYGIEALARWHDPLHGHVPPSRFIPLAEEIGEIENIGRW 610
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 353 VLDAALASAVHWRQKGIALP-VSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRDL 431
PRK11359 611 VIAEACRQLAEWRSQNIHIPaLSVNLSALHFRSNQLPNQVSDAMHAWGIDGHQLTVEITESMMMEHDTEIFKRIQILRDM 690
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 432 GVRLSCDDFGTGTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGC 511
PRK11359 691 GVGLSVDDFGTGFSGLSRLVSLPVTEIKIDKSFVDRCLTEKRILALLEAITSIGQSLNLTVVAEGVETKEQFEMLRKIHC 770
|
410 420
....*....|....*....|...
gi 117928031 512 TTGQGYYFSPPVPGALIGDVLRP 534
PRK11359 771 RVIQGYFFSRPLPAEEIPGWMSS 793
|
|
|
|
|
|
|
-1 |
| 139666 |
PRK13561 |
PRK13561 |
putative phosphodiesterase; Provisional |
putative phosphodiesterase; Provisional |
false |
true |
false |
651 |
3e-52 |
201.92 |
63.90 |
6,103,223,31,138,254,98,238,352,11,249,364,208,457,575,15,475,590,49 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 104 HRRASEHAGRDDLTGVANRPALLAALDDTFEdihrRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHR 183
PRK13561 224 YEEQNENAMRFPVSDLPNKALLMALLEQVVA----RKQTTALMIITCETLRDTAGVLKEAQREILLLTLVEKLKSVLSPR 299
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 184 DVVARLGADEFAVLLRDFNRPEGADAMSRAILRALREPFDVAGLPLTLDVAAGlaVAPRDADTSAE-LLRRAMVALQAAR 262
PRK13561 300 MVLAQISGYDFAIIANGVKEPWHAITLGQQVLTIINERLPIQRIQLRPSCSIG--IAMFYGDLTAEqLYSRAVSAAFTAR 377
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 263 HARSPAVENYRPAHDPAGAERLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQ 342
PRK13561 378 RKGKNQIQFFDPQQMEAAQKRLTEESDILNALENHQFAIWLQPQVEMRSGKLVSAEALLRMQQPDGSWDLPDGLIDRIES 457
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 343 SELIGLVTSYVLDAALASAVHWRQKGIALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPAD 422
PRK13561 458 CGLMVTVGHWVLEESCRLLAAWQERGIMLPLSVNLSALQLMHPNMVADMLELLTRYRIQPGTLILEVTESRRIDDPHAAV 537
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 423 AVAKKLRDLGVRLSCDDFGTGTTPLPRLRDLPLAE---LKIDNTLIAGIVGDDdkrAIVAAVVELGRVFDLTVVAEGIER 499
PRK13561 538 AILRPLRNAGVRIALDDFGMGYAGLRQLQHMKSLPidvLKIDKMFVDGLPEDS---SMVAAIIMLAQSLNLQMIAEGVET 614
|
410 420
....*....|....*....|....*
gi 117928031 500 QDEREVLIRLGCTTGQGYYFSPPVP 524
PRK13561 615 EAQRDWLAKAGVGVAQGFLFARPLP 639
|
|
|
|
|
|
|
-1 |
| 137515 |
PRK09776 |
PRK09776 |
putative sensor protein; Provisional |
putative sensor protein; Provisional |
false |
true |
false |
1116 |
1e-43 |
172.97 |
40.32 |
12,88,653,10,98,665,3,101,678,24,125,705,16,144,721,61,206,782,14,220,797,63,283,862,37,320,900,38,358,941,5,365,946,5,372,951,152 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 89 ATPVSQLQGG--GTT----------ATHRRASEHAGRDDLTGVANRPAL---LAALDDTFEDIHRRAAyagLLVVNIRGF 153
PRK09776 654 IAPLSTLDGEniGSVlvfqdvtesrAMLRQLSYSASHDALTGLANRASFekqLREALQTVNSTHQRHA---LVFIDLDRF 730
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 154 KQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLGADEFAVLLRDFNRPEgADAMSRAILRALRE-PFDVAGLPLTLD 232
PRK09776 731 KAVNDSAGHAAGDALLRELASLMLSMLRSSDVLARLGGDEFGLLLPDCNVES-ARFIATRIISAINDyRFPWEGRVYRVG 809
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 233 VAAGLAVAPRDADTSAELLRRAMVALQAARHARSPAVENYRPAHDPAGAER--LTLHAELDAALRTGQLVLHYQSTVDLA 310
PRK09776 810 ASAGITAIDDNNHQASEVMSQADIACYAAKNAGRGRVTVYEPQQAAAHSERreLSLAEQWRSMLEENQLMLQAQEIASPR 889
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 311 TGRTVGVEAL-LRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYVLDAAL---ASAVHwrQKGIAlpVSVNISARDLHDPS 386
PRK09776 890 IPEARNLWLIsLRLWDCEGEIIDEGAFRPAAEDPALMHALDRWVIHELFqqgARAVA--SKGLS--IAIPLSVASLSSAT 965
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 387 FPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRDLGVRLSCDDFGTGTTPLPRLRDLPLAELKIDNTLIA 466
PRK09776 966 LLPFLLEQLENSPLPPRLLHLEITETALLNHAEAASRLVQKLRLAGCRVVLDDFGRGLSSFNYLKAFMADYLKIDGELCA 1045
|
410 420 430 440 450
....*....|....*....|....*....|....*....|....*....|....*...
gi 117928031 467 GIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPPVP 524
PRK09776 1046 NLQGNLMDEMLVSIINGIAQRLGMKTIAGPVELPLTLDTLSGIGVDLAQGYVIGRPQP 1103
|
|
|
|
|
|
|
-1 |
| 138768 |
PRK11829 |
PRK11829 |
biofilm formation regulator HmsP; Provisional |
biofilm formation regulator HmsP; Provisional |
false |
true |
false |
728 |
2e-43 |
172.58 |
56.73 |
4,112,301,23,136,324,321,457,648,26,486,674,40 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 113 RDDLTGVANRPALLAALDDTFEDiHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLGAD 192
PRK11829 302 RFPVTELPNRSLFISLLEKEIAS-STRTDHFHLLVIGIETLQEVSGAMSEAQHQQLLLTIVQRIEQCIDDSDLLAQLSKT 380
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 193 EFAVLLRDFNRPEGADAMSRAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHARSPAVENY 272
PRK11829 381 EFAVLARGTRRSFPAMQLARRIMSQVTQPLFFDEITLRPSASIGITRYQAQQDTAESMMRNASTAMMAAHHEGRNQIMVF 460
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 273 RPAHDPAGAERLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSY 352
PRK11829 461 EPHLIEKTHKRLTQENDLLQAIENHDFTLFLQPQWDMKRQQVIGAEALLRWCQPDGSYVLPSGFVHFAEEEGMMVPLGNW 540
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 353 VLDAALASAVHWRQKGIALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAKKLRDLG 432
PRK11829 541 VLEEACRILADWKARGVSLPLSVNISGLQVQNKQFLPHLKTLISHYHIDPQQLLLEITETAQIQDLDEALRLLRELQGLG 620
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 433 VRLSCDDFGTGTTPLPRLRDLPLAE---LKIDNTLIAGIVGDDDKRAIVAAVVElgrVFDLTVVAEGIERQDEREVLIRL 509
PRK11829 621 LLIALDDFGIGYSSLRYLNHLKSLPihmIKLDKSFVKNLPEDDAIARIISCVSD---VLKVRVMAEGVETEEQRQWLLEH 697
|
410
....*....|....*..
gi 117928031 510 GCTTGQGYYFSPPVPGA 526
PRK11829 698 GIQCGQGFLFSPPLPRA 714
|
|
|
|
|
|
|
-1 |
| 34551 |
COG4943 |
COG4943 |
Predicted signal transduction protein containing sensor and EAL domains [Signal transduction mechanisms] |
Predicted signal transduction protein containing sensor and EAL domains [Signal... |
false |
true |
false |
524 |
2e-41 |
165.90 |
45.99 |
2,282,265,143,426,408,98 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 283 RLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYVLDAALASAV 362
COG4943 266 YLSPRRRLQRAIERRELCVHYQPIVDLATGKCVGAEALARWPQEDGTVVSPDVFIPLAEESGMIEQITDYVIRNVFRDLG 345
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 363 HWRQKGIALPVSVNISARDLHDPSFPDRVDTLLHLHGVPADRLTLEITETTLNSRLYPADAVAkKLRDLGVRLSCDDFGT 442
COG4943 346 DLLRQHRDLHVSINLSASDLASPRLIDRLNRKLAQYQVRPQQIALELTERTFADPKKMTPIIL-RLREAGHEIYIDDFGT 424
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 443 GTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPP 522
COG4943 425 GYSNLHYLQSLPVDALKIDKSFVDTLGTDSASHLIAPHIIEMAKSLGLKIVAEGVETEEQVDWLRKRGVHYGQGWLFSKA 504
|
..
gi 117928031 523 VP 524
COG4943 505 LP 506
|
|
|
|
|
|
|
-1 |
| 137979 |
PRK10551 |
PRK10551 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
518 |
3e-27 |
118.62 |
46.72 |
7,282,260,70,353,330,14,369,344,6,375,354,12,389,366,17,406,385,11,418,396,106 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 283 RLTLHAELDAALRTGQLVLHYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAAEQSELIGLVTSYvLDAALASAV 362
PRK10551 261 RMRPGREILTAIKREQFYVVYQPVVDTQTLRVTGLEVLLRWRHPTAGEIPPDAFINYAEAQKLIVPLTQH-LFELIARDA 339
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 363 HWRQKgiALPVSV----NISARDLHDPSFpdRVDTLLHLHGVPADRLT--LEITETTLNSRlYPADAVAKKLRDLGVRLS 436
PRK10551 340 AELQK--VLPVGAklgiNIAPAHLHSDSF--KADVQRLLASLPADHFQivLEITERDMLQE-EEALKLFAWLHSQGIEIA 414
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 437 CDDFGTGTTPLPRLRDLPLAELKIDNTLIAGIVGDDDKRAIVAAVVELGRVFDLTVVAEGIERQDEREVLIRLGCTTGQG 516
PRK10551 415 IDDFGTGHSALIYLERFTLDYLKIDRGFINAIGTETVTSPVLDAVLTLAKRLNMLTVAEGVETPEQARWLREHGVNFLQG 494
|
....*...
gi 117928031 517 YYFSPPVP 524
PRK10551 495 YWISRPLP 502
|
|
|
|
|
|
|
-1 |
| 138376 |
PRK11059 |
PRK11059 |
regulatory protein CsrD; Provisional |
regulatory protein CsrD; Provisional |
false |
true |
false |
642 |
2e-16 |
83.01 |
64.49 |
20,109,226,71,180,298,6,186,305,19,206,324,12,222,336,15,237,354,42,279,399,5,284,405,2,289,407,12,302,419,41,346,460,6,352,469,16,370,485,21,391,507,23,414,533,6,423,539,18,446,557,15,463,572,3,466,578,10,476,592,48 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 110 HAGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRV-RHRDVV-A 187
PRK11059 227 NAFLDAKTGLGNRLFFDNQLDTLLEDQEKVGAHGVVMLIRLPDFDLLQEELGESQVDELLFELINLLSTFVqRYPGALlA 306
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 188 RLGADEFAVLLRDFNRPEgADAMSRAILRALrepfDVAGLPLTLDVAAGL---AVAPRDADTSAELLRRAMVALQAARHA 264
PRK11059 307 RYSRSDFAVLLPHRSLKE-ADSLASQLLKAV----DSLPPPKMLDRDDFLhigIAAYRSGQSTEQVMEEAEMALRSAQLQ 381
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 265 RSPAVENYRPAHDPA---GAERL-TLhaeLDAALRTGQLVLhYQSTVDLATGRTVGVEALLRWQHPRRGLLRPAEFLPAA 340
PRK11059 382 GGNSWFMYDKAQDPEkgrGSVRWrTL---LEQALVRGGPRL-YQQPVVTRDGQVHHRELMCRIRDGQGNEVRAAEFMPMV 457
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 341 EQSeliGLVTSY---VLDAALASAVHWRQKGiaLPVSVNISARDLHDPSFPDRV-DTLLHLHGVPADRLTLEITETTL-- 414
PRK11059 458 LQC---GLSEQYdrqVIERVLPLLSYWPEES--QNLSINLSVDSLLSRAFQRWLrDTLLQCERSQRKRLIFELAEADVvq 532
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 415 -NSRLYPadaVAKKLRDLGVRLSCDDFGtgttpLPRLRDLPLAELKIDntLIA---GIVGDDDKRA----IVAAVVELGR 486
PRK11059 533 hIDRLRP---VLRMLRGLGCRLAVDQAG-----LTVVSTSYIKELNVE--LIKlhpSLVRNIHQRTenqlFVRSLVGACA 602
|
410 420 430
....*....|....*....|....*....|....*...
gi 117928031 487 VFDLTVVAEGIERQDEREVLIRLGCTTGQGYYFSPPVP 524
PRK11059 603 GTETQVFAEGVESREEWQTLQILGVSGGQGDFFASPQP 640
|
|
|
|
|
|
|
-1 |
| 33501 |
COG3706 |
PleD |
Response regulator containing a CheY-like receiver domain and a GGDEF domain [Signal transduction mechanisms] |
Response regulator containing a CheY-like receiver domain and a GGDEF domain [Signal... |
false |
true |
false |
435 |
3e-16 |
81.89 |
40.69 |
2,99,258,112,211,372,63 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 100 TTATHRRASEHAGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASR 179
COG3706 259 LRESLERLQELALVDGLTGLFNRRYFDEHLADLWKRALREGRPLSLLMLDIDDFKEINDTYGHDVGDEVLRQVARRLRQT 338
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 180 VRHRDVVARLGADEFAVLLRDFNRPEGADAMS--RAILRALREPFDVAGLPLTLDVAAGLAVAPRDADTSAELLRRAMVA 257
COG3706 339 VRGLDLVARYGGEEFAVVLPDTDLEAAIAIAEriRQKINELPFVHELSREPLEVTISIGVAEGKPGEDSIEELLKRADKA 418
|
170
....*....|....*..
gi 117928031 258 LQAARHARSPAVENYRP 274
COG3706 419 LYKAKASGRNRVVVKRA 435
|
|
|
|
|
|
|
-1 |
| 137400 |
PRK09581 |
pleD |
response regulator PleD; Reviewed |
response regulator PleD; Reviewed |
false |
true |
false |
457 |
1e-14 |
76.88 |
34.35 |
4,108,289,94,203,383,15,218,399,17,235,418,28 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 109 EHAGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVAR 188
PRK09581 290 EMAVTDGLTGLHNRRYFDMHLKQLIERANERGKPLSLMMLDIDHFKQVNDTYGHDAGDEVLREFAKRLRKNIRGTDLIAR 369
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 117928031 189 LGADEFAVLLRDFNrPEGADAMSRAILRAL-REPFDVAGLPLTLDVAA--GLAVAPRDADTSAELLRRAMVALQAARH 263
PRK09581 370 YGGEEFVVVMPDTD-IEVAIAVAERIRRKIaEEPFAISDGKERLNVTVsiGVAELRPSGESIEALIKRADKALYEAKN 446
|
|
|
|
|
|
|
-1 |
| 137615 |
PRK09966 |
PRK09966 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
407 |
3e-12 |
68.51 |
38.82 |
3,110,247,33,144,280,82,226,365,40 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 111 AGRDDLTGVANRPALLAALDDTFEDIHRRAAYAgLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLG 190
PRK09966 248 ALHDPLTGLANRAAFRSGINTLMNNSDARKTSA-LLFLDGDNFKYINDTWGHATGDRVLIEIAKRLAEFGGLRHKAYRLG 326
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 117928031 191 ADEFAVLLRDFNRPEGADAMSRAILRALREPFDVAG---LPLTLDVAAGLAVAPRDADTSAELLRRAMVALQAARHARS 266
PRK09966 327 GDEFAMVLYDVQSESEVQQICSALTQIFNLPFDLHNghqTTMTLSIGYAMTIEHASAEKLQELADHNMYQAKHQRAEKL 405
|
|
|
|
|
|
|
-1 |
| 137770 |
PRK10245 |
adrA |
diguanylate cyclase AdrA; Provisional |
diguanylate cyclase AdrA; Provisional |
false |
true |
false |
371 |
1e-11 |
66.84 |
43.94 |
5,101,199,3,104,203,109,213,314,8,225,322,3,228,326,36 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 102 ATH-RRASEHAGRDDLTGVANRPALLAALDDTFEDIHRRAAYAGLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRV 180
PRK10245 200 AEHkRRLQVMSTRDGMTGVYNRRHWETMLRNEFDNCRRHNRDATLLIIDIDHFKSINDTWGHDVGDEAIVALTRQLQITL 279
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 181 RHRDVVARLGADEFAVLLRDFNRPEGADAMSRA--ILRALREPfdvaGLP-LTLDVAAGLAVAPRDADTSAELLRRAMVA 257
PRK10245 280 RGSDVIGRFGGDEFAVIMSGTPAESAITAMLRVheGLNTLRLP----NAPqVTLRISVGVAPLNPQMSHYREWLKSADLA 355
|
....*..
gi 117928031 258 LQAARHA 264
PRK10245 356 LYKAKKA 362
|
|
|
|
|
|
|
-1 |
| 137576 |
PRK09894 |
PRK09894 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
293 |
1e-11 |
66.66 |
50.85 |
5,112,131,30,144,161,68,214,229,6,220,237,23,244,260,20 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 113 RDDLTGVANRPALLAALDDTFEDIHRRAAYagLLVVNIRGFKQINAIVGHSAADQLLTNIAMRLASRVRHRDVVARLGAD 192
PRK09894 132 MDVLTGLPGRRVLDESFDHQLRNREPLNLY--LALLDIDRFKLVNDTYGHLIGDVVLRTLATYLASWTRPYETVYRYGGE 209
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....
gi 117928031 193 EFAVLLRDFNRPEGADAMSRaiLRALRE--PFDVAGLPLTLDVAAGLAVAPRDaDTSAELLRRAMVALQAARHA 264
PRK09894 210 EFIIILKAATDEEACRAGER--IRQLIAnqAITHSEGRINITATFGVTRAFPE-EPLDEVIGRADRAMYEGKQA 280
|
|
|
|
|
|
|
-1 |
| 33240 |
COG3434 |
COG3434 |
Predicted signal transduction protein containing EAL and modified HD-GYP domains [Signal transduction mechanisms] |
Predicted signal transduction protein containing EAL and modified HD-GYP domains [... |
false |
true |
false |
407 |
4e-04 |
41.80 |
27.52 |
5,400,81,14,414,96,7,424,103,40,468,143,20,492,163,30 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928031 401 PADRLTLEITETTL-NSRLYPAdavAKKLRDLGVRLSCDDFGTGTTPLPRLRDLPLAELKIDNTLiagiVGDDDKRAIVA 479
COG3434 82 PPDKVVIEILEDCPpTEKLLSA---IKELKQKGYLLALDDFIFSNVSEWKPLLPLSDIVKIDFKR----VTFDKARLFDR 154
|
90 100 110 120
....*....|....*....|....*....|....*....|...
gi 117928031 480 AVVELGRVFdltvVAEGIERQDEREVLIRLGCTTGQGYYFSPP 522
COG3434 155 DLGYINKKF----LAEKVETEEEFEQAKKAGFDLFQGYFFSKP 193
|
|
|
|
|
|
|
-1 |
|