| 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 |
1e-53 |
207.37 |
99.17 |
3,695,2,77,774,79,31,805,114,126 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 696 LDRGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQGRTQLRDatG 775
cd01948 3 LRRALERGEFELYYQPIVDLRTGRIVGYEALLRWRHPEGGLISPAEFIPLAEETGLIVELGRWVLEEACRQLARWQA--G 80
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 776 QRNWRTSVNLSLEELRREGAIERLLPLITR----PSALDIEVSASSLLDHSEETLGLLDALRARGARLIVDDFGDGASSL 851
cd01948 81 GPDLRLSVNLSARQLRDPDFLDRLLELLAEtglpPRRLVLEITESALIDDLEEALATLRRLRALGVRIALDDFGTGYSSL 160
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 852 TALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPPLSAGD 931
cd01948 161 SYLKRLPVDYLKIDRSFVRDIETDPEDRAIVRAIIALAHSLGLKVVAEGVETEEQLELLRELGCDYVQGYLFSRPLPAEE 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-13 |
71.85 |
98.73 |
5,523,0,27,550,31,38,589,69,25,614,97,24,638,123,32 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 524 HDGLTGLLNRSGLRAALGQATAAQTGG----MVACLDIDGFGGLNAALSRTAGDLLLIQVAARLNDLAElEGGQAARLAD 599
cd01949 1 TDPLTGLPNRRAFEERLERLLARARRSgrplALLLIDLDHFKQINDTYGHAAGDEVLKEVARRLRSSLR-ESDLVARLGG 79
|
90 100 110 120 130 140 150
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*.
gi 15805776 600 DTFAVYLPQLGAAVG---GQKLQAALREPLRTGKRLVPVTFS--LGAAPLLAAAPEQALADAEVALQHARRQGRGQ 670
cd01949 80 DEFAILLPGTDLEEAeelAERLRKAIEEPFFIDGEEIRVTASigIAEYPEDGEDLEELLRRADKALYQAKRSGRNR 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... |
0 |
| 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 |
4e-53 |
205.17 |
97.66 |
3,690,2,75,768,77,37,805,118,134 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 691 QLRAVLDRGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQgrtQL 770
COG2200 3 QLERDLRQALENGEFSLYYQPIVDLATGRIVGYEALLRWRHPDGGLISPGEFIPLAEETGLIVELGRWVLEEACR---QL 79
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 771 RDATGQRNWRTSVNLSLEELRREGAIERLLPLITR----PSALDIEVSASSLLDHSEETLGLLDALRARGARLIVDDFGD 846
COG2200 80 RTWPRAGPLRLAVNLSPVQLRSPGLVDLLLRLLARlglpPHRLVLEITESALIDDLDTALALLRQLRELGVRIALDDFGT 159
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 847 GASSLTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPP 926
COG2200 160 GYSSLSYLKRLPPDILKIDRSFVRDLETDARDQAIVRAIVALAHKLGLTVVAEGVETEEQLDLLRELGCDYLQGYLFSRP 239
|
250
....*....|...
gi 15805776 927 LSAGDLVTWVQGR 939
COG2200 240 LPADALDALLSSS 252
|
|
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 |
| 128367 |
smart00052 |
EAL |
Putative diguanylate phosphodiesterase |
Putative diguanylate phosphodiesterase |
false |
false |
false |
241 |
6e-50 |
194.74 |
97.93 |
4,697,5,68,768,73,8,776,82,29,805,115,126 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 698 RGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQgrtQLRDATGQ- 776
smart00052 6 QALENGQFLLYYQPIVSLRTGRLVGVEALIRWQHPEGGIISPDEFIPLAEETGLIVPLGRWVLEQACQ---QLAEWQAQg 82
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 777 RNWRTSVNLSLEELRREGAIERLLPLITR----PSALDIEVSASSLLDHSEETLGLLDALRARGARLIVDDFGDGASSLT 852
smart00052 83 PPLRISINLSARQLISPDLVPRVLELLEEtglpPQRLELEITESVLLDDDESAVATLQRLRELGVRIALDDFGTGYSSLS 162
|
170 180 190 200 210 220 230
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 15805776 853 ALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPPLSAGD 931
smart00052 163 YLKRLPVDLLKIDKSFVRDLQTDPEDEAIVQSIIELAQKLGLQVVAEGVETPEQLDLLRSLGCDYGQGYLFSRPLPLDD 241
|
|
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 |
1e-42 |
170.29 |
100.00 |
6,692,0,73,768,73,11,779,88,23,802,114,38,841,152,32,874,184,52 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 693 RAVLDRGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQgrtQLRD 772
pfam00563 1 EQALREALENGEFSLYFQPIVDLRTGKVLGYEALLRWQHPDGGLIPPDEFLPLAERLGLIAELDRWVLEKALA---QLAE 77
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 773 ATGQRNW----RTSVNLSLEELRREGAIERLLPL---ITRPSALDIEVSASSLLDHSEETLGLLDALRARGARLIvDDFG 845
pfam00563 78 WRGNALLppdlPLSVNLSPASLLDPSFLEALLALkqgGLPPSRLVLEITESDLDEDLRLLEALARLRSLGFRLAL-DDFG 156
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 846 DGASSLTALTQFPLYGVKLHPTLTTRLPgDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTP 925
pfam00563 157 TGYSSLSYLSRLPPDYIKIDRSFIKDLS-DPESRALLRALIALARELGIKVVAEGVETEEQLELLKELGIDYVQGYLFSK 235
|
.
gi 15805776 926 P 926
pfam00563 236 P 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 |
| 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 |
4e-14 |
75.54 |
98.90 |
5,504,2,47,551,53,37,589,90,21,610,114,28,638,145,36 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 505 LRDVTTLRRAQAKLRHDASHDGLTGLLNRSGLRAALGQATAAQTGGM----VACLDIDGFGGLNAALSRTAGDLLLIQVA 580
COG2199 3 LRLLTRLRKAEERLERLALHDPLTGLPNRRAFEERLERALARARRHGeplaLLLLDLDHFKQINDTYGHAAGDEVLREVA 82
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 581 ARLNDLAElEGGQAARLADDTFAVYLPQLG---AAVGGQKLQAALREPLRTGKRLVPVTFS---LGAAPLLAAAPEQALA 654
COG2199 83 RRLRSNLR-EGDLVARLGGDEFAVLLPGTSleeAARLAERIRAALEEPFFLGGEELRVTVSigvALYPEDGSDDAELLLR 161
|
170 180
....*....|....*....|
gi 15805776 655 DAEVALQHARRQGRGQLTVF 674
COG2199 162 RADLALYRAKRAGRNRVVVF 181
|
|
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 |
2e-11 |
67.27 |
100.00 |
5,519,0,31,550,35,38,589,73,20,609,96,29,638,127,36 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 520 HDASHDGLTGLLNRSGLRAALGQATAAQTGG----MVACLDIDGFGGLNAALSRTAGDLLLIQVAARLNDLAElEGGQAA 595
smart00267 1 RLAFRDPLTGLPNRRYFEEELEQELQRAQRQgspfALLLIDLDNFKDINDTYGHAVGDELLQEVAQRLSSCLR-PGDLLA 79
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 596 RLADDTFAVYLPQL---GAAVGGQKLQAALREPLRTGKRLVPVTFS--LGAAPLLAAAPEQALADAEVALQHARRQGRGQ 670
smart00267 80 RLGGDEFALLLPETsleEAIALAERILQQLREPIIIHGIPLYLTISigVAAYPNPGEDAEDLLKRADTALYQAKKAGRNQ 159
|
....
gi 15805776 671 LTVF 674
smart00267 160 VAVY 163
|
|
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 |
| 110022 |
pfam00990 |
GGDEF |
GGDEF domain |
GGDEF domain |
false |
false |
false |
160 |
6e-10 |
61.88 |
100.00 |
5,521,0,12,533,16,55,589,71,21,610,98,28,638,128,32 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 522 ASHDGLTGLLNR----SGLRAALGQATAAQTGGMVACLDIDGFGGLNAALSRTAGDLLLIQVAARLNDLAElEGGQAARL 597
pfam00990 1 AAHDPLTGLPNRryfeEELEQELQRAQRRQSPLALLLLDLDNFKRINDTYGHAVGDEVLQEVAQRLSSSLR-RSDLVARL 79
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 598 ADDTFAVYLPQLG------AAVGGQKLQAALREPLRTGKRLVPVTFS--LGAAPLLAAAPEQALADAEVALQHARRQGRG 669
pfam00990 80 GGDEFAILLPDTSlegaqeLAERIRRLLAALKIPHTLSGLPLYVTISigIAAYPNDGEDAEDLLKRADQALYQAKNQGRN 159
|
.
gi 15805776 670 Q 670
pfam00990 160 R 160
|
|
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 |
| 137662 |
PRK10060 |
PRK10060 |
RNase II stability modulator; Provisional |
RNase II stability modulator; Provisional |
false |
true |
false |
663 |
1e-48 |
190.71 |
66.37 |
11,500,215,54,554,271,29,585,300,9,594,310,18,612,331,17,631,348,4,635,356,58,697,414,19,717,433,57,776,490,29,805,523,132 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 501 LLLSLRDVTTLRRAQAKLRHDASHDGLTGLLNRSGLRAALGQATAAQTGGMVAC--LDIDGFGGLNAALSRTAGDLLLIQ 578
PRK10060 216 LICSGTDITEERRAQERLRILANTDSITGLPNRNAIQELIDHAIAQADNNQVGIvyLDLDNFKKVNDAYGHMFGDQLLQD 295
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 579 VAARLndLAELEGGQA-ARLADDTFAVYLPQLGAA---VGGQKLQAALREPLRTGkrLVPV----TFSLGAAPLLAAAPE 650
PRK10060 296 VSLAI--LSCLEEDQTlARLGGDEFLVLASHTSQAaleAMASRILTRLRLPFRIG--LIEVytgcSIGIALSPEHGDDSE 371
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 651 QALADAEVALQHARRQGRGQLTVFEPDMRAEEAQTFELEDQLRavldRGLQHEQFSLLYQPAVSLKdGRVLGAEALLRWT 730
PRK10060 372 SLIRSADTAMYTAKEGGRGQFCVFSPEMNQRVFEYLWLDTNLR----KALENDQLVIHYQPKITWR-GEVRSLEALVRWQ 446
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 731 HPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQGRTQLRDATgqRNWRTSVNLSLEELRREGAIERLLPLITR----P 806
PRK10060 447 SPERGLIPPLEFISYAEESGLIVPLGRWVILDVVRQAAKWRDKG--INLRVAVNVSARQLADQTIFTALKQVLQElnfeY 524
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 807 SALDIEVSASSLLDHSEETLGLLDALRARGARLIVDDFGDGASSLTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTV 886
PRK10060 525 CPIDVELTESCLIENEELALSVIQQFSQLGAQVHLDDFGTGYSSLSQLARFPIDAIKLDQSFVRDIHKQPVSQSLVRAIV 604
|
410 420 430 440 450
....*....|....*....|....*....|....*....|....*....|.
gi 15805776 887 SLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPPLSAGDLVTWVQ 937
PRK10060 605 AVAQALNLQVIAEGVETAKEDAFLTKNGVNERQGFLFAKPMPAVAFERWYK 655
|
|
|
|
|
|
|
-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 |
7e-44 |
174.44 |
63.65 |
10,511,217,22,533,243,50,583,295,6,592,301,19,611,324,14,625,340,70,700,410,4,704,415,70,779,485,26,805,515,124 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 512 RRAQAKLRHDASHDGLTGLLNR----SGLRAALGQATAAQTGGMVACLDIDGFGGLNAALSRTAGDLLLIQVAARL--ND 585
COG5001 218 RRLSDENDRLANLDSLTGLPNRrrffAELDARLAAARQSGRRLVLGVIDLDGFKPVNDAFGHATGDRLLIEVGRRLkaFD 297
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 586 LAELeggQAARLADDTFAVYLPQLGA----AVGGQKLQAALREP--LRTGKRLVPVTFSLGAAPLLAAAPEQALADAEVA 659
COG5001 298 GAPI---LAARLGGDEFALIIPALEDdalrVAGARALCESLQAPydLRGVRVQVGASIGIAPFPSGADTSEQLFERADYA 374
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 660 LQHARRQGRGQLTVFEPDMRAEEAQTFELEDQLRAVldrglQHEQ-FSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVS 738
COG5001 375 LYHAKQNGKGAAVLFDARHEAAIRDMAVVEQALRSA-----DLEQeLSVHFQPIVDIVSGKTIALEALARWHSPEIGPVP 449
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 739 PARFLPLAQRSDLITSIGEWVVREAVQGRTQLRDATgqrnwRTSVNLSLEELRREGAIERLLPLITR----PSALDIEVS 814
COG5001 450 PDVFIGIAERSGQIVELTRLLLAKALREARAWPMDV-----RVSINLSARDLASMENVRRLLAIVSEsciaPHRLDFEIT 524
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 815 ASSLLDHSEETLGLLDALRARGARLIVDDFGDGASSLTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGL 894
COG5001 525 ETAIVCDFDQARDALAALHELGVRTALDDFGTGYSSLSHLRALPLDKIKIDRSFVSDLEENPTSEDIVRTVLQLGRNLRM 604
|
410 420 430
....*....|....*....|....*....|....*
gi 15805776 895 TVTAVGVETYAQLDMLRDLGCDAAQGYALTPPLSA 929
COG5001 605 ECVVEGVETEAQRDRVAALGATVMQGYHYARPMPA 639
|
|
|
|
|
|
|
-1 |
| 138538 |
PRK11359 |
PRK11359 |
cAMP phosphodiesterase; Provisional |
cAMP phosphodiesterase; Provisional |
false |
true |
false |
799 |
3e-43 |
172.33 |
51.69 |
8,524,378,61,587,439,6,593,446,17,610,466,83,697,549,75,773,624,20,793,647,13,806,661,130 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 525 DGLTGLLNRSGLRAALGQATAAQTGGMVACLDIDGFGGLNAALSRTAGDLLLIQVAARLNDlaELEGGQ-AARLADDTFA 603
PRK11359 379 DPMTGLPNRNNLHNYLDDLVDKAVSPVVYLIGVDHIQDVIDSLGYAWADQALLEVVNRFRE--KLKPDQyLCRIEGTQFV 456
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 604 VYLPQLG---AAVGGQKLQAALREPLRTGKRLVPVTFSLGAAPLLAAAPEQALADAEVALQHARRQGRGQLTVFEPDMRA 680
PRK11359 457 LVSLENDvsnITQIADELRNVVSKPIMIDDKPFPLTLSIGISYDVGKNRDYLLSTAHNAMDYIRKNGGNGWQFFSPAMNE 536
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 681 EEAQTFELEDQLRavldRGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVV 760
PRK11359 537 MVKERLVLGAALK----EAISNNQLKLVYQPQIFAETGELYGIEALARWHDPLHGHVPPSRFIPLAEEIGEIENIGRWVI 612
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 761 REAVQGRTQLRDaTGQRNWRTSVNLSLEELRRE---GAIERLLPLITRP-SALDIEVSASSLLDHSEETLGLLDALRARG 836
PRK11359 613 AEACRQLAEWRS-QNIHIPALSVNLSALHFRSNqlpNQVSDAMHAWGIDgHQLTVEITESMMMEHDTEIFKRIQILRDMG 691
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 837 ARLIVDDFGDGASSLTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCD 916
PRK11359 692 VGLSVDDFGTGFSGLSRLVSLPVTEIKIDKSFVDRCLTEKRILALLEAITSIGQSLNLTVVAEGVETKEQFEMLRKIHCR 771
|
410 420
....*....|....*....|
gi 15805776 917 AAQGYALTPPLSAGDLVTWV 936
PRK11359 772 VIQGYFFSRPLPAEEIPGWM 791
|
|
|
|
|
|
|
-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 |
5e-33 |
138.55 |
47.14 |
4,691,268,82,775,350,28,803,382,37,841,419,96 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 692 LRAVLDRGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQGRTQLR 771
COG4943 269 PRRRLQRAIERRELCVHYQPIVDLATGKCVGAEALARWPQEDGTVVSPDVFIPLAEESGMIEQITDYVIRNVFRDLGDLL 348
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 772 DAtgQRNWRTSVNLSLEELRREGAIERLLPLI----TRPSALDIEVSASSLLDHSEETLGLLDALRARGARLIvDDFGDG 847
COG4943 349 RQ--HRDLHVSINLSASDLASPRLIDRLNRKLaqyqVRPQQIALELTERTFADPKKMTPIILRLREAGHEIYI-DDFGTG 425
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 848 ASSLTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPPL 927
COG4943 426 YSNLHYLQSLPVDALKIDKSFVDTLGTDSASHLIAPHIIEMAKSLGLKIVAEGVETEEQVDWLRKRGVHYGQGWLFSKAL 505
|
250
....*....|
gi 15805776 928 SAGDLVTWVQ 937
COG4943 506 PAQAFLDWAE 515
|
|
|
|
|
|
|
-1 |
| 139666 |
PRK13561 |
PRK13561 |
putative phosphodiesterase; Provisional |
putative phosphodiesterase; Provisional |
false |
true |
false |
651 |
4e-27 |
118.72 |
40.40 |
8,662,375,15,677,391,17,699,408,66,765,476,9,778,485,27,805,516,52,857,571,19,879,590,48 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 663 ARRQGRGQLTVFEPD-MRAEEAQTFELEDQLRAvldrgLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPAR 741
PRK13561 376 ARRKGKNQIQFFDPQqMEAAQKRLTEESDILNA-----LENHQFAIWLQPQVEMRSGKLVSAEALLRMQQPDGSWDLPDG 450
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 742 FLPLAQRSDLITSIGEWVVREAVQ--GRTQLRDATgqrnWRTSVNLSLEELRREGAIERLLPLITR----PSALDIEVSA 815
PRK13561 451 LIDRIESCGLMVTVGHWVLEESCRllAAWQERGIM----LPLSVNLSALQLMHPNMVADMLELLTRyriqPGTLILEVTE 526
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 816 SSLLDHSEETLGLLDALRARGARLIVDDFGDGASSLTALTQF---PLYGVKLHPTLTTRLPGDQkslKLVQGTVSLAHSL 892
PRK13561 527 SRRIDDPHAAVAILRPLRNAGVRIALDDFGMGYAGLRQLQHMkslPIDVLKIDKMFVDGLPEDS---SMVAAIIMLAQSL 603
|
250 260 270
....*....|....*....|....*....|....*
gi 15805776 893 GLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPPL 927
PRK13561 604 NLQMIAEGVETEAQRDWLAKAGVGVAQGFLFARPL 638
|
|
|
|
|
|
|
-1 |
| 137515 |
PRK09776 |
PRK09776 |
putative sensor protein; Provisional |
putative sensor protein; Provisional |
false |
true |
false |
1116 |
3e-24 |
109.41 |
39.25 |
12,502,668,31,533,703,48,581,757,6,594,763,20,614,786,10,624,797,37,661,836,28,691,864,25,716,890,55,774,945,31,805,980,118,923,1100,6 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 503 LSLRDVTTLRRAQAKLRHDASHDGLTGLLNR----SGLRAALGQATAAQTGGMVACLDIDGFGGLNAALSRTAGDLLLIQ 578
PRK09776 669 LVFQDVTESRAMLRQLSYSASHDALTGLANRasfeKQLREALQTVNSTHQRHALVFIDLDRFKAVNDSAGHAAGDALLRE 748
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 579 VAA------RLNDLAeleggqaARLADDTFAVYLPQLGAAVG---GQKLQAALRE-PLRTGKRLVPVTFSLGAAPLLAAA 648
PRK09776 749 LASlmlsmlRSSDVL-------ARLGGDEFGLLLPDCNVESArfiATRIISAINDyRFPWEGRVYRVGASAGITAIDDNN 821
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 649 PEQALADAEVALQ--HARRQGRGQLTVFEPDMRAEEAQTFELEdqLRAVLDRGLQHEQFSLLYQPAVSLK-DGRVLGAEA 725
PRK09776 822 HQASEVMSQADIAcyAAKNAGRGRVTVYEPQQAAAHSERRELS--LAEQWRSMLEENQLMLQAQEIASPRiPEARNLWLI 899
|
250 260 270 280 290 300 310 320
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 726 LLRWTHPELGNVSPARFLPLAQRSDLITSIGEWVVREAVQGRTQLRdatGQRNWRTSVNLSLEELRREGAIERLLPLITR 805
PRK09776 900 SLRLWDCEGEIIDEGAFRPAAEDPALMHALDRWVIHELFQQGARAV---ASKGLSIAIPLSVASLSSATLLPFLLEQLEN 976
|
330 340 350 360 370 380 390 400
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 806 ----PSALDIEVSASSLLDHSEETLGLLDALRARGARLIVDDFGDGASSLTALTQFPLYGVKLHPTLTTRLPGDQKSLKL 881
PRK09776 977 splpPRLLHLEITETALLNHAEAASRLVQKLRLAGCRVVLDDFGRGLSSFNYLKAFMADYLKIDGELCANLQGNLMDEML 1056
|
410 420 430 440 450
....*....|....*....|....*....|....*....|....*....|
gi 15805776 882 VQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYAL--TPPLSA 929
PRK09776 1057 VSIINGIAQRLGMKTIAGPVELPLTLDTLSGIGVDLAQGYVIgrPQPLDL 1106
|
|
|
|
|
|
|
-1 |
| 138768 |
PRK11829 |
PRK11829 |
biofilm formation regulator HmsP; Provisional |
biofilm formation regulator HmsP; Provisional |
false |
true |
false |
728 |
4e-22 |
102.47 |
36.13 |
7,662,448,31,697,479,74,772,553,4,777,557,28,805,589,45,850,637,33,886,670,41 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 663 ARRQGRGQLTVFEPDMRAEEAQTFELEDQLRavldRGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARF 742
PRK11829 449 AHHEGRNQIMVFEPHLIEKTHKRLTQENDLL----QAIENHDFTLFLQPQWDMKRQQVIGAEALLRWCQPDGSYVLPSGF 524
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 743 LPLAQRSDLITSIGEWVVREAVQGRTQLRdATGQrNWRTSVNLSLEELRREGAIERLLPLITR----PSALDIEVSASSL 818
PRK11829 525 VHFAEEEGMMVPLGNWVLEEACRILADWK-ARGV-SLPLSVNISGLQVQNKQFLPHLKTLISHyhidPQQLLLEITETAQ 602
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 819 LDHSEETLGLLDALRARGARLIVDDFGDGASS---LTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQgtvSLAHSLGLT 895
PRK11829 603 IQDLDEALRLLRELQGLGLLIALDDFGIGYSSlryLNHLKSLPIHMIKLDKSFVKNLPEDDAIARIIS---CVSDVLKVR 679
|
250 260 270
....*....|....*....|....*....|..
gi 15805776 896 VTAVGVETYAQLDMLRDLGCDAAQGYALTPPL 927
PRK11829 680 VMAEGVETEEQRQWLLEHGIQCGQGFLFSPPL 711
|
|
|
|
|
|
|
-1 |
| 137979 |
PRK10551 |
PRK10551 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
518 |
1e-17 |
87.42 |
46.33 |
6,697,269,55,752,328,22,779,350,15,794,368,7,801,376,39,841,415,94 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 698 RGLQHEQFSLLYQPAVSLKDGRVLGAEALLRWTHPELGNVSPARFLPLAQRSDLI----TSIGEWVVREAVQGRTQLRDA 773
PRK10551 270 TAIKREQFYVVYQPVVDTQTLRVTGLEVLLRWRHPTAGEIPPDAFINYAEAQKLIvpltQHLFELIARDAAELQKVLPVG 349
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 774 TgqrnwRTSVNLSLEELRREG---AIERLLP-LITRPSALDIEVSASSLLDHSEETLGLLDALRARGARLIvDDFGDGAS 849
PRK10551 350 A-----KLGINIAPAHLHSDSfkaDVQRLLAsLPADHFQIVLEITERDMLQEEEALKLFAWLHSQGIEIAI-DDFGTGHS 423
|
170 180 190 200 210 220 230 240
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 850 SLTALTQFPLYGVKLHPTLTTRLPGDQKSLKLVQGTVSLAHSLGLTVTAVGVETYAQLDMLRDLGCDAAQGYALTPPLSA 929
PRK10551 424 ALIYLERFTLDYLKIDRGFINAIGTETVTSPVLDAVLTLAKRLNMLTVAEGVETPEQARWLREHGVNFLQGYWISRPLPL 503
|
....*.
gi 15805776 930 GDLVTW 935
PRK10551 504 DDFVKW 509
|
|
|
|
|
|
|
-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-05 |
46.07 |
34.02 |
5,499,247,34,533,285,55,589,340,18,607,361,17,624,381,14 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 500 ELLLSLRDVTTLRRAQAKLRHDASHDGLTGLLNR----SGLRAALGQATAAQTGGMVACLDIDGFGGLNAALSRTAGDLL 575
COG3706 248 RQLRRKRYERQLRESLERLQELALVDGLTGLFNRryfdEHLADLWKRALREGRPLSLLMLDIDDFKEINDTYGHDVGDEV 327
|
90 100 110 120 130 140
....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 15805776 576 LIQVAARLNDLAElEGGQAARLADDTFAVYLP---QLGAAVGGQKLQAALRE---PLRTGKRLVPVTFS 638
COG3706 328 LRQVARRLRQTVR-GLDLVARYGGEEFAVVLPdtdLEAAIAIAERIRQKINElpfVHELSREPLEVTIS 395
|
|
|
|
|
|
|
-1 |
| 137615 |
PRK09966 |
PRK09966 |
hypothetical protein; Provisional |
hypothetical protein; Provisional |
false |
true |
false |
407 |
1e-04 |
44.24 |
28.50 |
4,510,236,45,555,284,27,585,311,7,592,320,32 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 511 LRRAQAKLRHDASHDGLTGLLNRSGLRAALGQATAAQTGGMVACL---DIDGFGGLNAALSRTAGDLLLIQVAARlndLA 587
PRK09966 237 LQAKNAQLLRTALHDPLTGLANRAAFRSGINTLMNNSDARKTSALlflDGDNFKYINDTWGHATGDRVLIEIAKR---LA 313
|
90 100 110
....*....|....*....|....*....|....*....
gi 15805776 588 ELEGG--QAARLADDTFAVYLPQLGAAVGGQKLQAALRE 624
PRK09966 314 EFGGLrhKAYRLGGDEFAMVLYDVQSESEVQQICSALTQ 352
|
|
|
|
|
|
|
-1 |
| 129332 |
TIGR00229 |
sensory_box |
PAS domain S-box |
PAS domain S-box |
true |
true |
false |
124 |
3e-04 |
42.66 |
79.03 |
5,164,24,31,195,58,29,226,87,10,236,98,16,253,114,8 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 165 FRQVSRTFLELFGLTGADVLGRTVHEVFPDH---AALAQQLDSAAAGRAVQLGDERVPSLPGHsgERWLRGSARP-YFGG 240
TIGR00229 25 ILYVNPAFEEIFGYSAEELIGRNVLELIPEEdreEVRERIERLLEGEREPYSEERRVRRKDGS--EIWVEVSVSPiRTNG 102
|
90 100
....*....|....*....|.
gi 15805776 241 AAAGVLWTVQDVsTEHTQTTQ 261
TIGR00229 103 GELGVVGIVRDI-TERKQAEE 122
|
|
|
|
|
|
|
-1 |
| 117025 |
pfam08448 |
PAS_4 |
PAS fold |
PAS fold |
false |
true |
false |
110 |
0.001 |
41.25 |
97.27 |
4,150,2,44,194,49,26,224,75,15,239,92,17 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 151 QLPAATAWLSAELEFRQVSRTFLELFGLTGADVLGRTVHEVFPD---HAALAQQLDSAAAGRAVQLGDERVPSlpghSGE 227
pfam08448 3 SLPDALAVLDPDGRVRYANAAAAELFGLPPEELLGKTLAELLPPedaARLERALRRALEGEEPIDFLEELLLN----GEE 78
|
90 100 110
....*....|....*....|....*....|.
gi 15805776 228 RWLRGSARPYFG--GAAAGVLWTVQDVSTEH 256
pfam08448 79 RHYELRLTPLRDpdGEVIGVLVISRDITERR 109
|
|
|
|
|
|
|
-1 |
| 137400 |
PRK09581 |
pleD |
response regulator PleD; Reviewed |
response regulator PleD; Reviewed |
false |
true |
false |
457 |
0.001 |
41.06 |
33.92 |
10,499,262,7,508,269,6,514,277,10,524,294,9,533,307,50,583,363,3,593,366,22,618,388,5,623,400,5,628,407,10 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 500 ELLLSLRdvTTLRRA--QAKLRHDASH-------DGLTGLLNR----SGLRAALGQATAAQTGGMVACLDIDGFGGLNAA 566
PRK09581 263 ELLARVR--TQIRRKryQDALRQNLEQsiemavtDGLTGLHNRryfdMHLKQLIERANERGKPLSLMMLDIDHFKQVNDT 340
|
90 100 110 120 130 140 150 160
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 567 LSRTAGDLLLIQVAARL------NDLaeleggqAARLADDTFAVYLPQLGAAVGGqklQAALR-------EPLRT--GKR 631
PRK09581 341 YGHDAGDEVLREFAKRLrknirgTDL-------IARYGGEEFVVVMPDTDIEVAI---AVAERirrkiaeEPFAIsdGKE 410
|
....*..
gi 15805776 632 LVPVTFS 638
PRK09581 411 RLNVTVS 417
|
|
|
|
|
|
|
-1 |
| 110021 |
pfam00989 |
PAS |
PAS fold |
PAS fold |
false |
true |
false |
112 |
0.003 |
39.31 |
95.54 |
4,147,5,46,193,53,30,225,83,13,238,98,14 |
10 20 30 40 50 60 70 80
....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 15805776 148 LITQLPAATAWLSAELEFRQVSRTFLELFGLTGADVLGRTVHEVFP--DHAALAQQLDSAAAGRAVQLGDERVPSLPGhs 225
pfam00989 6 ILESLPDGIFVVDEDGRILYVNAAAEELLGLSREEVIGKSLLDLIPedDDAVAELLRQALLQGEESRGFEVSFRVSDG-- 83
|
90 100
....*....|....*....|....*....
gi 15805776 226 GERWLRGSARPYF--GGAAAGVLWTVQDV 252
pfam00989 84 RPRHVEVRASPVRdaGGEILGFLGVLRDI 112
|
|
|
|
|
|
|
-1 |
|