| 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 |
5e-69 |
257.83 |
100.00 |
3,485,0,79,566,79,104,670,184,56 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 486 TELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQRe 565
cd01948 1 ADLRRALERGEFELYYQPIVDLRTGRIVGYEALLRWRHPEGGLISPAEFIPLAEETGLIVELGRWVLEEACRQLARWQA- 79
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 566 lGEAPFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLARLEELKLLGVSLAVDDFGARYS 645
cd01948 80 -GGPDLRLSVNLSARQLRDPDFLDRLLELLAETGLPPRRLVLEITESALIDDLEEALATLRRLRALGVRIALDDFGTGYS 158
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 646 SLAGLPRLPLDMVKIDQAFIDAVGT-PEGSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPVDT 724
cd01948 159 SLSYLKRLPVDYLKIDRSFVRDIETdPEDRAIVRAIIALAHSLGLKVVAEGVETEEQLELLRELGCDYVQGYLFSRPLPA 238
|
..
gi 117928641 725 DR 726
cd01948 239 EE 240
|
|
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 |
5e-40 |
161.22 |
90.45 |
1,311,0,142 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 312 HDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARYGGD 391
cd01949 1 TDPLTGLPNRRAFEERLERLLARARRSGRPLALLLIDLDHFKQINDTYGHAAGDEVLKEVARRLRSSLRESDLVARLGGD 80
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|..
gi 117928641 392 EFVALLHDTDVRGAAIVAARIIDAVRQPLRVGEMDVTVDASIGIACSVAGGTAADDLLRSAD 453
cd01949 81 EFAILLPGTDLEEAEELAERLRKAIEEPFFIDGEEIRVTASIGIAEYPEDGEDLEELLRRAD 142
|
|
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 |
3e-67 |
251.75 |
98.34 |
3,484,0,83,569,83,96,665,180,57 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 485 ETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQR 564
smart00052 1 ERELRQALENGQFLLYYQPIVSLRTGRLVGVEALIRWQHPEGGIISPDEFIPLAEETGLIVPLGRWVLEQACQQLAEWQA 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 565 ELGeaPFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLARLEELKLLGVSLAVDDFGARY 644
smart00052 81 QGP--PLRISINLSARQLISPDLVPRVLELLEETGLPPQRLELEITESVLLDDDESAVATLQRLRELGVRIALDDFGTGY 158
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 117928641 645 SSLAGLPRLPLDMVKIDQAFI-DAVGTPEGSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPV 722
smart00052 159 SSLSYLKRLPVDLLKIDKSFVrDLQTDPEDEAIVQSIIELAQKLGLQVVAEGVETPEQLDLLRSLGCDYGQGYLFSRPL 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 |
| 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 |
5e-65 |
244.46 |
98.83 |
3,483,3,81,567,84,103,670,188,68 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 484 LETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQ 563
COG2200 4 LERDLRQALENGEFSLYYQPIVDLATGRIVGYEALLRWRHPDGGLISPGEFIPLAEETGLIVELGRWVLEEACRQLRTWP 83
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 564 RelgEAPFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLARLEELKLLGVSLAVDDFGAR 643
COG2200 84 R---AGPLRLAVNLSPVQLRSPGLVDLLLRLLARLGLPPHRLVLEITESALIDDLDTALALLRQLRELGVRIALDDFGTG 160
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 644 YSSLAGLPRLPLDMVKIDQAFIDAVGT-PEGSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPV 722
COG2200 161 YSSLSYLKRLPPDILKIDRSFVRDLETdARDQAIVRAIVALAHKLGLTVVAEGVETEEQLDLLRELGCDYLQGYLFSRPL 240
|
250
....*....|....*.
gi 117928641 723 DTDRVPALRPTAQRLW 738
COG2200 241 PADALDALLSSSQSRV 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 |
5e-57 |
217.67 |
100.00 |
4,484,0,78,562,79,31,594,110,19,614,129,107 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 485 ETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAW-Q 563
pfam00563 1 EQALREALENGEFSLYFQPIVDLRTGKVLGYEALLRWQHPDGGLIPPDEFLPLAERLGLIAELDRWVLEKALAQLAEWrG 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 564 RELGEAPFTISVNVSTAQLAGDTFAGYLKEvLENTGLAATSLVLDITEALvLREEPWLLARLEELKLLGVSLAVDDFGAR 643
pfam00563 81 NALLPPDLPLSVNLSPASLLDPSFLEALLA-LKQGGLPPSRLVLEITESD-LDEDLRLLEALARLRSLGFRLALDDFGTG 158
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 117928641 644 YSSLAGLPRLPLDMVKIDQAFIDAVGTPEGSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEP 721
pfam00563 159 YSSLSYLSRLPPDYIKIDRSFIKDLSDPESRALLRALIALARELGIKVVAEGVETEEQLELLKELGIDYVQGYLFSKP 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-36 |
148.16 |
91.88 |
2,309,0,109,418,112,35 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 310 AFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARYG 389
pfam00990 1 AAHDPLTGLPNRRYFEEELEQELQRAQRRQSPLALLLLDLDNFKRINDTYGHAVGDEVLQEVAQRLSSSLRRSDLVARLG 80
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|....*..
gi 117928641 390 GDEFVALLHDTDVRGAAIVAARIIDAVRQ---PLRVGEMDVTVDASIGIACSVAGGTAADDLLRSAD 453
pfam00990 81 GDEFAILLPDTSLEGAQELAERIRRLLAAlkiPHTLSGLPLYVTISIGIAAYPNDGEDAEDLLKRAD 147
|
|
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 |
7e-36 |
147.39 |
88.96 |
1,308,1,145 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 309 RAFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARY 388
smart00267 2 LAFRDPLTGLPNRRYFEEELEQELQRAQRQGSPFALLLIDLDNFKDINDTYGHAVGDELLQEVAQRLSSCLRPGDLLARL 81
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 117928641 389 GGDEFVALLHDTDVRGAAIVAARIIDAVRQPLRVGEMDVTVDASIGIACSVAGGTAADDLLRSAD 453
smart00267 82 GGDEFALLLPETSLEEAIALAERILQQLREPIIIHGIPLYLTISIGVAAYPNPGEDAEDLLKRAD 146
|
|
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 |
9e-30 |
127.16 |
80.11 |
2,309,19,127,436,147,17 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 310 AFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARYG 389
COG2199 20 ALHDPLTGLPNRRAFEERLERALARARRHGEPLALLLLDLDHFKQINDTYGHAAGDEVLREVARRLRSNLREGDLVARLG 99
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 117928641 390 GDEFVALLHDTDVRGAAIVAARIIDAVRQPLRVGEMDVTVDASIGIA-CSVAGGTAADDLLRSAD 453
COG2199 100 GDEFAVLLPGTSLEEAARLAERIRAALEEPFFLGGEELRVTVSIGVAlYPEDGSDDAELLLRRAD 164
|
|
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 |
5e-29 |
124.75 |
89.09 |
3,308,0,110,418,113,7,426,120,27 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 309 RAFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARY 388
TIGR00254 1 QAVRDPLTGLYNRRYLEEMLDSELKRARRFQRSFSVLMIDIDNFKKINDTLGHDVGDEVLREVARILQSSVRGSDVVGRY 80
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 117928641 389 GGDEFVALLHDTDVRGAAIVAARIIDAVRQ---PLRVGEMdVTVDASIGIACSVAGGTAADDLLRSAD 453
TIGR00254 81 GGEEFVVILPGTPLEDALSKAERLRDAINSkpiEVAGSET-LTVTVSIGVACYPGHGLTLEELLKRAD 147
|
|
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 |
9e-05 |
44.31 |
39.22 |
2,634,154,26,660,181,73 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 635 LAVDDFGARYSSLAGLPRLPLDMVKI-DQAFIDAVGTPEGSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFA 713
PRK11596 155 LWLDDFGTGMANFSALSEVRYDYIKVaRELFVMLRQSPEGRTLFSQLLHLMNRYCRGVIVEGVETPEEWRDVQRSPAFAA 234
|
90 100
....*....|....*....|
gi 117928641 714 QGYLFAEPVDTDRVPALRPT 733
PRK11596 235 QGYFLSRPAPFDTLETLPLA 254
|
|
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 |
| 128379 |
smart00065 |
GAF |
Domain present in phytochromes and cGMP-specific phosphodiesterases. |
Domain present in phytochromes and cGMP-specific phosphodiesterases. |
true |
false |
false |
149 |
3e-04 |
42.75 |
97.99 |
5,180,3,21,201,27,35,236,75,14,250,90,7,257,98,51 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 181 DILDAVVRTVHEVLGVDTVII---RRGPSATVAARCGGTERTARWLARLPLPDGTTGGV-------------HDLETANP 244
smart00065 4 ELLQTILEELRQLLGADRVLIylvDEDDRGELVLVAADGLTLPLLGLRYPLGEGLAGRVaetgrplnipdveADPVFALD 83
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 117928641 245 PAGIAV-TRALAGV-VHENGRIAGALIAATTDPARLWRDADREALGVFADHVTLAITDATTVEAMN 308
smart00065 84 LLGRYQgVRSFLAVpLVADGELVGVLALHNKDSPRPFTEEDEELLQALANQLAIALANAQLYEELR 149
|
|
cl00853 |
140972 |
GAF |
GAF domain |
GAF domain |
-1 |
| 137662 |
PRK10060 |
PRK10060 |
RNase II stability modulator; Provisional |
RNase II stability modulator; Provisional |
false |
true |
false |
663 |
7e-79 |
290.48 |
61.09 |
6,312,239,22,336,261,171,508,432,57,565,490,2,570,492,100,670,593,51 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 313 DSLTGLASRALFLDRLNLGLAQaaRSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARYGGDE 392
PRK10060 240 DSITGLPNRNAIQELIDHAIAQ--ADNNQVGIVYLDLDNFKKVNDAYGHMFGDQLLQDVSLAILSCLEEDQTLARLGGDE 317
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 393 FVALLHDTDVRGAAIVAARIIDAVRQPLRVGEMDVTVDASIGIACSVAGGTAADDLLRSADVAMYRAKRAGRGRYAIYEP 472
PRK10060 318 FLVLASHTSQAALEAMASRILTRLRLPFRIGLIEVYTGCSIGIALSPEHGDDSESLIRSADTAMYTAKEGGRGQFCVFSP 397
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 473 SMHAALLEQLHLETELRGALHRGEFVVHYQPIVELaTGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVL 552
PRK10060 398 EMNQRVFEYLWLDTNLRKALENDQLVIHYQPKITW-RGEVRSLEALVRWQSPERGLIPPLEFISYAEESGLIVPLGRWVI 476
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 553 RTACAQARAWQRE-LGeapFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLARLEELKLL 631
PRK10060 477 LDVVRQAAKWRDKgIN---LRVAVNVSARQLADQTIFTALKQVLQELNFEYCPIDVELTESCLIENEELALSVIQQFSQL 553
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 632 GVSLAVDDFGARYSSLAGLPRLPLDMVKIDQAFIDAVGT-PEGSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARC 710
PRK10060 554 GAQVHLDDFGTGYSSLSQLARFPIDAIKLDQSFVRDIHKqPVSQSLVRAIVAVAQALNLQVIAEGVETAKEDAFLTKNGV 633
|
410
....*....|.
gi 117928641 711 EFAQGYLFAEP 721
PRK10060 634 NERQGFLFAKP 644
|
|
|
|
|
|
|
-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-68 |
254.18 |
69.08 |
5,278,196,140,418,337,148,571,485,94,665,580,60,725,641,13 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 279 WRDADREALGVFADHVTLAITDATTVEAMNRAFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDT 358
COG5001 197 YREFSDMVQSQVTLTQRAEETRRLSDENDRLANLDSLTGLPNRRRFFAELDARLAAARQSGRRLVLGVIDLDGFKPVNDA 276
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 359 LGHAAGDVLLVEIANRLRSCLRASDTAARYGGDEFVALLHDTDVRGAAIVAARIIDAVRQ-PLRVGEMDVTVDASIGIAC 437
COG5001 277 FGHATGDRLLIEVGRRLKAFDGAPILAARLGGDEFALIIPALEDDALRVAGARALCESLQaPYDLRGVRVQVGASIGIAP 356
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 438 SVAGGTAADDLLRSADVAMYRAKRAGRGRYAIYEPSMHAALLEQLHLETELRGALHRGEFVVHYQPIVELATGDILGAEA 517
COG5001 357 FPSGADTSEQLFERADYALYHAKQNGKGAAVLFDARHEAAIRDMAVVEQALRSADLEQELSVHFQPIVDIVSGKTIALEA 436
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 518 LLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQRELgeapfTISVNVSTAQLAGDTFAGYLKEVLEN 597
COG5001 437 LARWHSPEIGPVPPDVFIGIAERSGQIVELTRLLLAKALREARAWPMDV-----RVSINLSARDLASMENVRRLLAIVSE 511
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 598 TGLAATSLVLDITEALVLREEPWLLARLEELKLLGVSLAVDDFGARYSSLAGLPRLPLDMVKIDQAFI-DAVGTPEGSAF 676
COG5001 512 SCIAPHRLDFEITETAIVCDFDQARDALAALHELGVRTALDDFGTGYSSLSHLRALPLDKIKIDRSFVsDLEENPTSEDI 591
|
410 420 430 440 450 460
....*....|....*....|....*....|....*....|....*....|....*....|...
gi 117928641 677 ARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPVDTD-RVPALRPTAQRLW 738
COG5001 592 VRTVLQLGRNLRMECVVEGVETEAQRDRVAALGATVMQGYHYARPMPAEeRRRRGRGAGPDVW 654
|
|
|
|
|
|
|
-1 |
| 138538 |
PRK11359 |
PRK11359 |
cAMP phosphodiesterase; Provisional |
cAMP phosphodiesterase; Provisional |
false |
true |
false |
799 |
3e-64 |
242.05 |
52.44 |
6,312,378,11,323,392,13,343,405,100,445,505,125,571,630,102,673,733,64 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 313 DSLTGLASRAL---FLDRLNLGLAQAArsgtnlcLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARYG 389
PRK11359 379 DPMTGLPNRNNlhnYLDDLVDKAVSPV-------VYLIGVDHIQDVIDSLGYAWADQALLEVVNRFREKLKPDQYLCRIE 451
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 390 GDEFVALLHDTDVRGAAIVAARIIDAVRQPLRVGEMDVTVDASIGIACSVAGGTaaDDLLRSADVAMYRAKRAGRGRYAI 469
PRK11359 452 GTQFVLVSLENDVSNITQIADELRNVVSKPIMIDDKPFPLTLSIGISYDVGKNR--DYLLSTAHNAMDYIRKNGGNGWQF 529
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 470 YEPSMHAALLEQLHLETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGS 549
PRK11359 530 FSPAMNEMVKERLVLGAALKEAISNNQLKLVYQPQIFAETGELYGIEALARWHDPLHGHVPPSRFIPLAEEIGEIENIGR 609
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 550 WVLRTACAQARAWQRELGEAPfTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLARLEELK 629
PRK11359 610 WVIAEACRQLAEWRSQNIHIP-ALSVNLSALHFRSNQLPNQVSDAMHAWGIDGHQLTVEITESMMMEHDTEIFKRIQILR 688
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 630 LLGVSLAVDDFGARYSSLAGLPRLPLDMVKIDQAFIDAVGTPEG-SAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRA 708
PRK11359 689 DMGVGLSVDDFGTGFSGLSRLVSLPVTEIKIDKSFVDRCLTEKRiLALLEAITSIGQSLNLTVVAEGVETKEQFEMLRKI 768
|
410 420
....*....|....*....|....*....
gi 117928641 709 RCEFAQGYLFAEPVDTDRVPALRPTAQRL 737
PRK11359 769 HCRVIQGYFFSRPLPAEEIPGWMSSVLPL 797
|
|
|
|
|
|
|
-1 |
| 139666 |
PRK13561 |
PRK13561 |
putative phosphodiesterase; Provisional |
putative phosphodiesterase; Provisional |
false |
true |
false |
651 |
4e-51 |
198.07 |
63.90 |
7,304,225,25,333,250,84,417,335,19,437,354,133,572,487,80,652,570,14,668,584,57 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 305 EAMNRAFHDSLTGLASRALFLDRLNlglaQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDT 384
PRK13561 226 EQNENAMRFPVSDLPNKALLMALLE----QVVARKQTTALMIITCETLRDTAGVLKEAQREILLLTLVEKLKSVLSPRMV 301
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 385 AARYGGDEFVALLHDTDVRGAAIVAARIIDAVR-QPLRVGEMDVTVDASIGIAcSVAGGTAADDLLRSADVAMYRAKRAG 463
PRK13561 302 LAQISGYDFAIIANGVKEPWHAITLGQQVLTIInERLPIQRIQLRPSCSIGIA-MFYGDLTAEQLYSRAVSAAFTARRKG 380
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 464 RGRYAIYEPSMHAALLEQLHLETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGE 543
PRK13561 381 KNQIQFFDPQQMEAAQKRLTEESDILNALENHQFAIWLQPQVEMRSGKLVSAEALLRMQQPDGSWDLPDGLIDRIESCGL 460
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 544 MVEIGSWVLRTACAQARAWQRELGEAPftISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLA 623
PRK13561 461 MVTVGHWVLEESCRLLAAWQERGIMLP--LSVNLSALQLMHPNMVADMLELLTRYRIQPGTLILEVTESRRIDDPHAAVA 538
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 624 RLEELKLLGVSLAVDDFGARYSSLAGLPR---LPLDMVKIDQAFIDavGTPEGSAFARKIVELAHTLDLQVIAEGVQTQQ 700
PRK13561 539 ILRPLRNAGVRIALDDFGMGYAGLRQLQHmksLPIDVLKIDKMFVD--GLPEDSSMVAAIIMLAQSLNLQMIAEGVETEA 616
|
410 420
....*....|....*....|....*
gi 117928641 701 QFEELRRARCEFAQGYLFAEPVDTD 725
PRK13561 617 QRDWLAKAGVGVAQGFLFARPLPIE 641
|
|
|
|
|
|
|
-1 |
| 137515 |
PRK09776 |
PRK09776 |
putative sensor protein; Provisional |
putative sensor protein; Provisional |
false |
true |
false |
1116 |
9e-46 |
180.29 |
38.89 |
7,295,668,14,309,687,118,427,806,54,481,862,37,518,900,49,570,949,95,665,1045,57 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 296 LAITDATTVEAMNR-----AFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVE 370
PRK09776 669 LVFQDVTESRAMLRqlsysASHDALTGLANRASFEKQLREALQTVNSTHQRHALVFIDLDRFKAVNDSAGHAAGDALLRE 748
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 371 IANRLRSCLRASDTAARYGGDEFVALLHDTDVRGAAIVAARIIDAVRQPLRVGEMDV-TVDASIGIACSVAGGTAADDLL 449
PRK09776 749 LASLMLSMLRSSDVLARLGGDEFGLLLPDCNVESARFIATRIISAINDYRFPWEGRVyRVGASAGITAIDDNNHQASEVM 828
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 450 RSADVAMYRAKRAGRGRYAIYEPSMHAALLEQ--LHLETELRGALHRGEFVVHYQPIVELATGDILGAEAL-LRWNHPRR 526
PRK09776 829 SQADIACYAAKNAGRGRVTVYEPQQAAAHSERreLSLAEQWRSMLEENQLMLQAQEIASPRIPEARNLWLIsLRLWDCEG 908
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 527 GLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQRELGeapFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLV 606
PRK09776 909 EIIDEGAFRPAAEDPALMHALDRWVIHELFQQGARAVASKG---LSIAIPLSVASLSSATLLPFLLEQLENSPLPPRLLH 985
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 607 LDITEALVLREEPWLLARLEELKLLGVSLAVDDFGARYSSLAGLPRLPLDMVKIDQAFI-DAVGTPEGSAFARKIVELAH 685
PRK09776 986 LEITETALLNHAEAASRLVQKLRLAGCRVVLDDFGRGLSSFNYLKAFMADYLKIDGELCaNLQGNLMDEMLVSIINGIAQ 1065
|
410 420 430
....*....|....*....|....*....|....*..
gi 117928641 686 TLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPV 722
PRK09776 1066 RLGMKTIAGPVELPLTLDTLSGIGVDLAQGYVIGRPQ 1102
|
|
|
|
|
|
|
-1 |
| 138768 |
PRK11829 |
PRK11829 |
biofilm formation regulator HmsP; Provisional |
biofilm formation regulator HmsP; Provisional |
false |
true |
false |
728 |
1e-42 |
169.88 |
57.14 |
7,306,295,7,313,303,25,339,328,78,417,407,153,572,560,76,648,639,20,670,659,52 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 307 MNRAFHD-SLTGLASRALFLDRLNLGLAQAARSgTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTA 385
PRK11829 296 MGRISHRfPVTELPNRSLFISLLEKEIASSTRT-DHFHLLVIGIETLQEVSGAMSEAQHQQLLLTIVQRIEQCIDDSDLL 374
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 386 ARYGGDEFVALLHDTDVRGAAIVAARIIDAVR-QPLRVGEMDVTVDASIGIACSVAGGTAADDLLRSADVAMYRAKRAGR 464
PRK11829 375 AQLSKTEFAVLARGTRRSFPAMQLARRIMSQVtQPLFFDEITLRPSASIGITRYQAQQDTAESMMRNASTAMMAAHHEGR 454
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 465 GRYAIYEPSMHAALLEQLHLETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEM 544
PRK11829 455 NQIMVFEPHLIEKTHKRLTQENDLLQAIENHDFTLFLQPQWDMKRQQVIGAEALLRWCQPDGSYVLPSGFVHFAEEEGMM 534
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 545 VEIGSWVLRTACAQARAWQRELGEAPftISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPWLLAR 624
PRK11829 535 VPLGNWVLEEACRILADWKARGVSLP--LSVNISGLQVQNKQFLPHLKTLISHYHIDPQQLLLEITETAQIQDLDEALRL 612
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 625 LEELKLLGVSLAVDDFGARYSSLA---GLPRLPLDMVKIDQAFIDAVgtPEGSAFARKIVELAHTLDLQVIAEGVQTQQQ 701
PRK11829 613 LRELQGLGLLIALDDFGIGYSSLRylnHLKSLPIHMIKLDKSFVKNL--PEDDAIARIISCVSDVLKVRVMAEGVETEEQ 690
|
410 420
....*....|....*....|.
gi 117928641 702 FEELRRARCEFAQGYLFAEPV 722
PRK11829 691 RQWLLEHGIQCGQGFLFSPPL 711
|
|
|
|
|
|
|
-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 |
7e-42 |
167.44 |
45.23 |
4,483,268,82,567,350,48,616,398,58,674,457,48 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 484 LETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQ 563
COG4943 269 PRRRLQRAIERRELCVHYQPIVDLATGKCVGAEALARWPQEDGTVVSPDVFIPLAEESGMIEQITDYVIRNVFRDLGDLL 348
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 564 RElgEAPFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLrEEPWLLARLEELKLLGVSLAVDDFGAR 643
COG4943 349 RQ--HRDLHVSINLSASDLASPRLIDRLNRKLAQYQVRPQQIALELTERTFA-DPKKMTPIILRLREAGHEIYIDDFGTG 425
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 644 YSSLAGLPRLPLDMVKIDQAFIDAVGTPEGS-AFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPV 722
COG4943 426 YSNLHYLQSLPVDALKIDKSFVDTLGTDSAShLIAPHIIEMAKSLGLKIVAEGVETEEQVDWLRKRGVHYGQGWLFSKAL 505
|
|
|
|
|
|
|
-1 |
| 137979 |
PRK10551 |
PRK10551 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
518 |
2e-29 |
125.94 |
45.56 |
4,484,264,82,567,346,52,620,398,52,672,451,49 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 485 ETELRGALHRGEFVVHYQPIVELATGDILGAEALLRWNHPRRGLLTAAEFVPIAEDCGEMVEIGSWVLRTACAQARAWQR 564
PRK10551 265 GREILTAIKREQFYVVYQPVVDTQTLRVTGLEVLLRWRHPTAGEIPPDAFINYAEAQKLIVPLTQHLFELIARDAAELQK 344
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 565 ELgEAPFTISVNVSTAQLAGDTFAGYLKEVLENTGLAATSLVLDITEALVLREEPwLLARLEELKLLGVSLAVDDFGARY 644
PRK10551 345 VL-PVGAKLGINIAPAHLHSDSFKADVQRLLASLPADHFQIVLEITERDMLQEEE-ALKLFAWLHSQGIEIAIDDFGTGH 422
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 117928641 645 SSLAGLPRLPLDMVKIDQAFIDAVGTPE-GSAFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEP 721
PRK10551 423 SALIYLERFTLDYLKIDRGFINAIGTETvTSPVLDAVLTLAKRLNMLTVAEGVETPEQARWLREHGVNFLQGYWISRP 500
|
|
|
|
|
|
|
-1 |
| 137400 |
PRK09581 |
pleD |
response regulator PleD; Reviewed |
response regulator PleD; Reviewed |
false |
true |
false |
457 |
2e-24 |
109.24 |
32.82 |
3,306,288,112,418,401,4,422,407,31 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 307 MNRAFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAA 386
PRK09581 289 IEMAVTDGLTGLHNRRYFDMHLKQLIERANERGKPLSLMMLDIDHFKQVNDTYGHDAGDEVLREFAKRLRKNIRGTDLIA 368
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 387 RYGGDEFVALLHDTDVRGAAIVAARIIDAVRQ-PLRV--GEMDVTVDASIGIACSVAGGTAADDLLRSAD 453
PRK09581 369 RYGGEEFVVVMPDTDIEVAIAVAERIRRKIAEePFAIsdGKERLNVTVSIGVAELRPSGESIEALIKRAD 438
|
|
|
|
|
|
|
-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 |
4e-24 |
108.47 |
35.86 |
2,300,260,118,418,381,35 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 301 ATTVEAMNRAFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLR 380
COG3706 261 ESLERLQELALVDGLTGLFNRRYFDEHLADLWKRALREGRPLSLLMLDIDDFKEINDTYGHDVGDEVLRQVARRLRQTVR 340
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 117928641 381 ASDTAARYGGDEFVALLHDTDVRGAAIVAARIIDAVRQ---PLRVGEMDVTVDASIGIACSVAGGTAADDLLRSAD 453
COG3706 341 GLDLVARYGGEEFAVVLPDTDLEAAIAIAERIRQKINElpfVHELSREPLEVTISIGVAEGKPGEDSIEELLKRAD 416
|
|
|
|
|
|
|
-1 |
| 138376 |
PRK11059 |
PRK11059 |
regulatory protein CsrD; Provisional |
regulatory protein CsrD; Provisional |
false |
true |
false |
642 |
3e-19 |
92.64 |
64.17 |
14,309,227,70,379,298,6,385,305,12,397,318,23,420,342,9,431,351,13,445,364,32,477,406,4,490,410,16,507,426,56,567,482,25,592,508,67,659,583,3,669,586,53 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 310 AFHDSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCL-RASDTA-AR 387
PRK11059 228 AFLDAKTGLGNRLFFDNQLDTLLEDQEKVGAHGVVMLIRLPDFDLLQEELGESQVDELLFELINLLSTFVqRYPGALlAR 307
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 388 YGGDEFVALL-HDTDVRGAAIVAARIIDAVRQPL-RVGEMDVTVdaSIGIACSVAGGTAaDDLLRSADVAMYRAKRAGRG 465
PRK11059 308 YSRSDFAVLLpHRSLKEADSLASQLLKAVDSLPPpKMLDRDDFL--HIGIAAYRSGQST-EQVMEEAEMALRSAQLQGGN 384
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 466 RYAIYEPSMHAA----------LLEQlhletelrgALHRGEFVVHYQPIVElATGDILGAEALLRWNHPRRGLLTAAEFV 535
PRK11059 385 SWFMYDKAQDPEkgrgsvrwrtLLEQ---------ALVRGGPRLYQQPVVT-RDGQVHHRELMCRIRDGQGNEVRAAEFM 454
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 536 PIAEDCGEMVEIGSWVLRTACAQARAWQrelgEAPFTISVNVSTAQLAGDTFAGYLK-EVLENTGLAATSLVLDITEALV 614
PRK11059 455 PMVLQCGLSEQYDRQVIERVLPLLSYWP----EESQNLSINLSVDSLLSRAFQRWLRdTLLQCERSQRKRLIFELAEADV 530
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 615 LREEPWLLARLEELKLLGVSLAVDDFGARYSSLAGLPRLPLDMVK--------IDQafidavgTPEGSAFARKIVELAHT 686
PRK11059 531 VQHIDRLRPVLRMLRGLGCRLAVDQAGLTVVSTSYIKELNVELIKlhpslvrnIHQ-------RTENQLFVRSLVGACAG 603
|
410 420 430
....*....|....*....|....*....|....*.
gi 117928641 687 LDLQVIAEGVQTQQQFEELRRARCEFAQGYLFAEPV 722
PRK11059 604 TETQVFAEGVESREEWQTLQILGVSGGQGDFFASPQ 639
|
|
|
|
|
|
|
-1 |
| 137576 |
PRK09894 |
PRK09894 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
293 |
6e-19 |
91.31 |
59.73 |
4,277,97,57,336,154,63,399,218,44,444,262,10 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 278 LWRDADREALGVFADHVTLAITDATTVEAMNRAFHDSLTGLASRALFLDRLNLGLAQaaRSGTNLCLLFIDLDRFKIVND 357
PRK09894 98 HWQDADFDAFQEGLLSFTAALTDYKIYLLTIRSNMDVLTGLPGRRVLDESFDHQLRN--REPLNLYLALLDIDRFKLVND 175
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 358 TLGHAAGDVLLVEIANRLRSCLRASDTAARYGGDEFVALLHD-TDVRGAAIVAARIIDAVRQPLRVGEMDVTVDASIGIA 436
PRK09894 176 TYGHLIGDVVLRTLATYLASWTRPYETVYRYGGEEFIIILKAaTDEEACRAGERIRQLIANQAITHSEGRINITATFGVT 255
|
170
....*....|....*...
gi 117928641 437 CSVAGGTaADDLLRSADV 454
PRK09894 256 RAFPEEP-LDEVIGRADR 272
|
|
|
|
|
|
|
-1 |
| 137615 |
PRK09966 |
PRK09966 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
407 |
2e-15 |
79.29 |
24.08 |
3,300,238,29,329,268,11,342,279,57 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 301 ATTVEAMNRAFHDSLTGLASRALFLDRLN-LGLAQAARSGTnlCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCL 379
PRK09966 239 AKNAQLLRTALHDPLTGLANRAAFRSGINtLMNNSDARKTS--ALLFLDGDNFKYINDTWGHATGDRVLIEIAKRLAEFG 316
|
90 100
....*....|....*....|
gi 117928641 380 RASDTAARYGGDEFVALLHD 399
PRK09966 317 GLRHKAYRLGGDEFAMVLYD 336
|
|
|
|
|
|
|
-1 |
| 137770 |
PRK10245 |
adrA |
diguanylate cyclase AdrA; Provisional |
diguanylate cyclase AdrA; Provisional |
false |
true |
false |
371 |
1e-09 |
60.68 |
23.72 |
1,312,212,88 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 313 DSLTGLASRALFLDRLNLGLAQAARSGTNLCLLFIDLDRFKIVNDTLGHAAGDVLLVEIANRLRSCLRASDTAARYGGDE 392
PRK10245 213 DGMTGVYNRRHWETMLRNEFDNCRRHNRDATLLIIDIDHFKSINDTWGHDVGDEAIVALTRQLQITLRGSDVIGRFGGDE 292
|
....*...
gi 117928641 393 FVALLHDT 400
PRK10245 293 FAVIMSGT 300
|
|
|
|
|
|
|
-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 |
8e-07 |
51.05 |
25.06 |
6,631,110,9,641,119,14,655,134,6,664,140,7,675,147,46,721,196,16 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 117928641 632 GVSLAVDDFgARYSSLAGLPRLPL-DMVKIDqafIDAVGTPegsaFARKIVELAHTLDLQVIAEGVQTQQQFEELRRARC 710
COG3434 111 GYLLALDDF-IFSNVSEWKPLLPLsDIVKID---FKRVTFD----KARLFDRDLGYINKKFLAEKVETEEEFEQAKKAGF 182
|
90 100 110
....*....|....*....|....*....|
gi 117928641 711 EFAQGYLFAEP---VDTDRVPALRPTAQRL 737
COG3434 183 DLFQGYFFSKPeiiKRGRLSPFLKTTIELL 212
|
|
|
|
|
|
|
-1 |
|