Protein Info for Pf6N2E2_3981 in Pseudomonas fluorescens FW300-N2E2

Annotation: T1SS secreted agglutinin RTX

These analyses and tools can help you predict a protein's function, but be skeptical. For enzymes, over 10% of annotations from KEGG or SEED are probably incorrect. For other types of proteins, the error rates may be much higher. MetaCyc and Swiss-Prot have low error rates, but the best hits in these databases are often quite distant, so this protein's function may not be the same. TIGRFam has low error rates. Finally, many experimentally-characterized proteins are not in any of these databases. To find relevant papers, use PaperBLAST.

Protein Families and Features

1 500 1000 1500 2000 2500 3000 3500 4000 4500 4986 PF20579: LapA" amino acids 173 to 271 (99 residues), 88.6 bits, see alignment (E = 1.5e-28) amino acids 273 to 370 (98 residues), 122.4 bits, see alignment (E = 4.3e-39) amino acids 373 to 470 (98 residues), 116.9 bits, see alignment (E = 2.2e-37) amino acids 473 to 570 (98 residues), 117.6 bits, see alignment (E = 1.4e-37) amino acids 573 to 670 (98 residues), 116.7 bits, see alignment (E = 2.7e-37) amino acids 673 to 776 (104 residues), 90.6 bits, see alignment (E = 3.7e-29) amino acids 779 to 882 (104 residues), 91.5 bits, see alignment (E = 1.9e-29) amino acids 885 to 988 (104 residues), 89 bits, see alignment (E = 1.1e-28) amino acids 991 to 1094 (104 residues), 92.2 bits, see alignment (E = 1.1e-29) amino acids 1097 to 1200 (104 residues), 90.9 bits, see alignment (E = 2.8e-29) amino acids 1203 to 1306 (104 residues), 90.2 bits, see alignment (E = 4.8e-29) amino acids 1309 to 1412 (104 residues), 93.1 bits, see alignment (E = 6.2e-30) amino acids 1415 to 1518 (104 residues), 90.2 bits, see alignment (E = 4.8e-29) amino acids 1521 to 1624 (104 residues), 89.7 bits, see alignment (E = 6.7e-29) amino acids 1627 to 1730 (104 residues), 90.9 bits, see alignment (E = 2.8e-29) amino acids 1733 to 1836 (104 residues), 90.2 bits, see alignment (E = 4.8e-29) amino acids 1839 to 1942 (104 residues), 89.5 bits, see alignment (E = 7.8e-29) amino acids 1945 to 2048 (104 residues), 89.5 bits, see alignment (E = 7.8e-29) amino acids 2051 to 2154 (104 residues), 93.1 bits, see alignment (E = 6.2e-30) amino acids 2157 to 2260 (104 residues), 90.2 bits, see alignment (E = 4.8e-29) amino acids 2263 to 2366 (104 residues), 89.7 bits, see alignment (E = 6.7e-29) amino acids 2369 to 2472 (104 residues), 90.9 bits, see alignment (E = 2.8e-29) amino acids 2475 to 2578 (104 residues), 90.2 bits, see alignment (E = 4.8e-29) amino acids 2581 to 2684 (104 residues), 89.5 bits, see alignment (E = 7.8e-29) amino acids 2687 to 2790 (104 residues), 89.5 bits, see alignment (E = 7.8e-29) amino acids 2793 to 2896 (104 residues), 91.5 bits, see alignment (E = 1.9e-29) amino acids 2899 to 3002 (104 residues), 90.4 bits, see alignment (E = 4.1e-29) amino acids 3005 to 3108 (104 residues), 91.6 bits, see alignment (E = 1.8e-29) amino acids 3111 to 3214 (104 residues), 91.9 bits, see alignment (E = 1.4e-29) amino acids 3217 to 3320 (104 residues), 91.5 bits, see alignment (E = 1.9e-29) amino acids 3323 to 3426 (104 residues), 91.5 bits, see alignment (E = 1.9e-29) amino acids 3429 to 3532 (104 residues), 90.4 bits, see alignment (E = 4.1e-29) amino acids 3535 to 3638 (104 residues), 94.2 bits, see alignment (E = 2.7e-30) amino acids 3641 to 3745 (105 residues), 95.8 bits, see alignment (E = 8.7e-31) amino acids 3747 to 3856 (110 residues), 45.2 bits, see alignment (E = 5.3e-15) PF03160: Calx-beta" amino acids 3760 to 3832 (73 residues), 27.2 bits, see alignment (E = 1.8e-09) PF16184: Cadherin_3" amino acids 3993 to 4092 (100 residues), 31.5 bits, see alignment (E = 7.4e-11) PF17963: Big_9" amino acids 3995 to 4094 (100 residues), 25.9 bits, see alignment (E = 6.6e-09) PF00353: HemolysinCabind" amino acids 4444 to 4464 (21 residues), 7 bits, see alignment (E = 0.0031) amino acids 4754 to 4770 (17 residues), 14.3 bits, see alignment (E = 1.6e-05) amino acids 4823 to 4855 (33 residues), 37.8 bits, see alignment (E = 7.1e-13) amino acids 4848 to 4881 (34 residues), 30.8 bits, see alignment (E = 1.1e-10) PF00092: VWA" amino acids 4476 to 4596 (121 residues), 36.7 bits, see alignment (E = 2.7e-12) PF13519: VWA_2" amino acids 4478 to 4592 (115 residues), 34 bits, see alignment (E = 2e-11) TIGR03661: type I secretion C-terminal target domain (VC_A0849 subclass)" amino acids 4892 to 4971 (80 residues), 57.7 bits, see alignment (E = 1.1e-19)

Best Hits

Predicted SEED Role

"T1SS secreted agglutinin RTX"

Sequence Analysis Tools

PaperBLAST (search for papers about homologs of this protein)

Search CDD (the Conserved Domains Database, which includes COG and superfam)

Search structures

Predict protein localization: PSORTb (Gram-negative bacteria)

Predict transmembrane helices and signal peptides: Phobius

Check the current SEED with FIGfam search

Find homologs in fast.genomics or the ENIGMA genome browser

See A0A160A2X3 at UniProt or InterPro

Protein Sequence (4986 amino acids)

>Pf6N2E2_3981 T1SS secreted agglutinin RTX (Pseudomonas fluorescens FW300-N2E2)
MSSVIAVVKSIVGQVFVVSPEGIRRVLIEGDRLNVGDQLDTGPAGAVTLELADGRTLDLG
RDTQWSANAPDSSTDLEQATAQAAPSVEELQQAIAAGVDPTTALEATAAGATAAGTGGAA
GGGHSFVVLDATAGSVDPTVGFPTEGLAAAAATDNNILGGDTTDTTANAVLNATMTLSAT
PTLTEAGGVLVYTATVTQAPQTALTVTLSNGAVIVIPAGQLTGSVNVPLAPNDTVYNDPS
QISVTVTGTTGGTGIAVTVPTTPAVTQITDTIDTTTVTLTAGNTVTEGGQITYTATLTNP
AQTPVTVTLSNGSVITIAAGQTTGTVNVETPANDVYNNGSTISTTITGATGGNFENLVPS
TTPAVTTITDSADTTGLTLTASNTITEGGQITYTATLTNPAQTPVTVTLSNGSVITIAAG
QTTGTVNVETPANDVYNNGSTVSTTITGATGGNFENLVPSATLAVTTITDSADTTGLTLT
ASNTITEGGQITYTATLTNPAQTPVTVTLSNGSVITIAAGQTTGTVNVETLANDVYNNGS
TVSTTITGATGGNFENLVPSTTPAVTTITDSADTTGLTLTASNTITEGGQITYTATLTNP
AQTPVTVTLSNGSVITIAAGQTTGTVNVETLANDVYNNGSTVSTTITGATGGNFENLVPS
TSPAVTTITDSVDTTTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGK
TITIAAGASSGVLDVAVGNDVYQGPTTVTESIVSASGGNLEAIAPNTAPVSTIVSDVNDT
TTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLD
VAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNEN
GTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAVGASSGVLDVAVGNDVYQGPTTV
TESIASASGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNENGTITYTATLTDANG
NPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEA
IAPNTAPVSTVVSDVNDTTSVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTL
DSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVSTVVSD
VNDTTSVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASS
GVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPT
VNENGTITYTATLTDANGNPVTAQNGPVTVTLESGKTITIAAGASSGVLDVAVGNDVYQG
PTTVTESIKDASGGNLEAIAPNTTPVSTVISDVNDTTSVTLTATPTVNENGTITYTATLT
DANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGG
NLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPV
TVTLDSGKTITIAVGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVST
VVSDVNDTTSVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAA
GASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVSTVVSDVNDITTVTLT
ATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGND
VYQGPTTVTESIASASGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNENGTITYT
ATLTDANGNPITAQNGPVTVTLESGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIST
ATGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNENGTITYTATLTDANGNPITAQ
NGPVTVTLESGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESISTATGGNLEAIAPNTA
PVSTIVSDVNDTTTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLESGKTI
TIAAGASSGVLDVAVGNDVYQGPTTVTESIKDASGGNLEAIAPNTTPVSTVISDVNDTTS
VTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVA
VGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNENGT
ITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAVGASSGVLDVAVGNDVYQGPTTVTE
SIASASGGNLEAIAPNTAPVSTVVSDVNDTTSVTLTATPTVNENGTITYTATLTDANGNP
VTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIA
PNTAPVSTVVSDVNDITTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDS
GKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPVSTIVSDVN
DTTTVTLTATPTVNENGTITYTATLTDANGNPITAQNGPVTVTLESGKTITIAAGASSGV
LDVAVGNDVYQGPTTVTESISTATGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVN
ENGTITYTATLTDANGNPITAQNGPVTVTLESGKTITIAAGASSGVLDVAVGNDVYQGPT
TVTESISTATGGNLEAIAPNTAPVSTIVSDVNDTTTVTLTATPTVNENGTITYTATLTDA
NGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNL
EAIAPNTAPVSTIVSDVNDTTSVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTV
TLDSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTSPVSTVV
SDVNDTTTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGA
SSGVLDVAVGNDVYQGPTTVTESISTATGGNLEAIAPNTTPVSTVVSDVNDTTTVTLTAT
PTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGNDVY
QGPTTVTESIASASGGNLEAIAPNTTPVSTIVSDVNDTTTVTLTATPTVNENGTITYTAT
LTDANGNPVTAQNGPVTVTLESGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASAS
GGNLEAIAPNTAPVSTVVSDVNDTTTVTLTATPTVNENGTITYTATLTDANGNPVTAQNG
PVTVTLDSGKTITIAAGASSGVLDVAVGNDVYQGPTTVTESIASASGGNLEAIAPNTAPV
STIVSDVNDTTTVTLTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITI
AAGASSGVLDVAVGNDVYQGPTTVTESISTATGGNLEAIAPNTAPVSTIVSDVNDTTTVT
LTATPTVNENGTITYTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVG
NDVYQGPTTVTESIKDASGGNLEAIAPNTTPVSTTVSDVNDTTTVTLTATPTVNENGTIT
YTATLTDANGNPVTAQNGPVTVTLDSGKTITIAAGASSGVLDVAVGNDVYTGAPSVTESI
KSASGGNLEAIGVDKTGASTAVGDTVDNTTVSITGSTSVAEGQAATYTVSLTNPAQTEVT
LKIVYSGTAADGTDFTGVYTVKIPANATSATFNVATLDDKITEGTENFVVKIDSATGGNF
EHLAVSGTNGSVSTSIIDNDAPPALDLDANNSSGKTGADYQVTFTEGTTGPGVSIADTDL
SITDPDSTLLTGATIVLTNRQPGDALNLGNSVNGISINANSTDGKVVLTLTGNATLADYM
QQIKNISFINNSEDPSTVPRIITVTVTDGASYSNTATTTVNVVGVNDAPVATGGAVTGTE
DTSLVLGWSTFGISDVDNSATSLGVKITELPADGKLQYLDGATWKDVANNQTFTKADIDA
GKLRFTPDANESGANGYVGSSTGNNQADYAQVKFQPTDGQALGNTGTVKIDITPVADAPT
LNVAGNNVTSTGLIKEVWTGLSGLGTDGSGAPSGTLKSVIDAAGTPNSSGTVTNVQSDSN
VNPGTASKTSGLIFLEAGKTYTFSGTGDDSLLVTIGGKTVAATTWGAGGQLNGSFTPTTS
GYYTLDIYHHNQTGPGSYDVNLSVNGSTPVDLNGAGVPLYTGVTDLTNAGVTVSDLHGTN
GEGYYDGFKLNEGAEGTSVHLSKITTALTDTDGSESLSVKIGGMPEGSVLSDGAGHFATV
GSNGEASVSGWNLGSLTLTPPAYYNGQFNLTVTSTSTEALGGSATSTAQIPVTVHPATYN
AVTATSGSDNVTGTDGNDIVVADIGGLTVVPGVNYNIAFMVDSSGSMSDSSIAAAKASLT
SVFNTLKQSLGSNSGTVNIFLADFDSQVNSTVSVNLNDSDALTQLKDLLDSMVSGGGTNY
EDVFKTTANFFKSTEALNNTGAKNLTYFITDGKPTYYQTGEQVNPTLYDSVKLDDVLSAA
NYSVGKYYTQTIDSTHKYTIYEDGKMYLSTKNGKKWTDSYVGVVHAEGNGTFELSNQGGT
GYGEYWNYVDSAAGSTDSFTLLKNLSTVEAIGLNSDVTLNDLKPYDSDSSPQTNIDPNNL
ANSIIGHTEATLPGSDTVNGGDGNDILFGDLVSFNGVTGEGYQAIQAFVAQQSGVDVSKV
TTSNVHQYITEHYTAFDVSGAHDGNDTLLGGAGNDIIFGQGGNDTLNGGKGNDILLGGTG
NDTLIGGQGNDTLIGGLGGDTFVWKSGDTGTDVIKNFNAGEGDRIDLRDLLQGETGSTID
HFLKISTVDGVSSLQVSTSGQFNTTNGGAATPDVTIKLEGNNWSNVNLNSLIAGSDPTIK
VDHNNS