Align Amino-acid permease RocE (characterized)
to candidate BWI76_RS19685 BWI76_RS19685 lysine transporter
Query= SwissProt::P39137 (467 letters) >FitnessBrowser__Koxy:BWI76_RS19685 Length = 489 Score = 376 bits (966), Expect = e-109 Identities = 187/457 (40%), Positives = 285/457 (62%), Gaps = 18/457 (3%) Query: 11 LQRTMKSRHLFMISLGGVIGTGFFLGTGFTINQAGPLGAVLSYLVGGFIMFLTMLCLGEL 70 L+R +K+RHL MI++GG IGTG F+ +G TI+QAGP GA+LSY++ G +++ M LGEL Sbjct: 13 LRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYILIGLMVYFLMTSLGEL 72 Query: 71 AVAFPVSGSFQTYATKFISPAFGFAFGWLYWLGWAVTCAIEFLSAGQLMQRWFPHIDVWI 130 A PVSGSF TY ++ FGFA GW YW WAVT A++ ++A +M WFP W+ Sbjct: 73 AAFMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQLVMTYWFPDAPGWV 132 Query: 131 WCLVFAALMFILNAITTKAFAESEFWFSGIKILIILLFIILGGAAMFGLIDLKGGEQAPF 190 W +F +MF+LN I+ K F E+E+WFS IK+ +++FII+G +FG+ KG + A + Sbjct: 133 WSALFLGIMFLLNWISVKGFGEAEYWFSLIKVATVIIFIIVGVMMIFGI--FKGAQPAGW 190 Query: 191 LTHFYEDGLFPNGIKAMLITMITVNFAFQGTELIGVAAGESEDPEKTIPRSIKQTVWRTL 250 +D F G AM+ + V F+FQGTELIG+AAGESE+PEK IPR+++Q WR L Sbjct: 191 SNWVIDDAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESENPEKNIPRAVRQVFWRIL 250 Query: 251 VFFVLSIIVIAGMIPWKQAGVVE--------SPFVAVFEQIGIPYAADIMNFVILIALLS 302 +F+V +I++I+ +IP+ ++ SPF VF+ G+ AA IMN VIL A+LS Sbjct: 251 LFYVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSAAAIMNAVILTAVLS 310 Query: 303 VANSGLYASTRILYAMANEGQAFKALGKTNQRGVPMYSLIVTMAVACLSLLTKFAQAETV 362 NSG+YASTR+LY +A +G+A + K ++ GVP +L T +A L L+ +TV Sbjct: 311 AGNSGMYASTRMLYTLACDGKAPRIFSKLSKGGVPRNALYATTVIAGLCFLSSMFGNQTV 370 Query: 363 YMVLLSLAGMSAQVGWITISLSQIMFRRKYIREGGKIEDLKFKTPLYPVLPLIGLTLNTV 422 Y+ LL+ +GM+ + W+ I++S FRR Y+ +G + DL +++ +P+ P+ L + Sbjct: 371 YLWLLNTSGMTGFIAWLGIAISHYRFRRGYVLQGNDLNDLPYRSGFFPLGPIFAFVLCLI 430 Query: 423 VLISLAFDPEQR--------IALYCGVPFMIICYIIY 451 + + ++ + A Y G+P ++ + Y Sbjct: 431 ITLGQNYEAFLKDTIDWGGVAATYIGIPLFLVIWFGY 467 Lambda K H 0.329 0.142 0.438 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 676 Number of extensions: 35 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 467 Length of database: 489 Length adjustment: 34 Effective length of query: 433 Effective length of database: 455 Effective search space: 197015 Effective search space used: 197015 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory