Align Histidine permease HisP (characterized)
to candidate BWI76_RS19685 BWI76_RS19685 lysine transporter
Query= SwissProt::A2RI97 (477 letters) >FitnessBrowser__Koxy:BWI76_RS19685 Length = 489 Score = 498 bits (1281), Expect = e-145 Identities = 237/469 (50%), Positives = 334/469 (71%), Gaps = 4/469 (0%) Query: 7 VKRNLKQRHITMIALGGTIGTGLFLTSGATISQAGPWGAVLAYCFIGIMVYFVMTSLGEM 66 ++R LK RH+TMIA+GG+IGTGLF+ SGATISQAGP GA+L+Y IG+MVYF+MTSLGE+ Sbjct: 13 LRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYILIGLMVYFLMTSLGEL 72 Query: 67 ATYLPTSGSFSDYGGRYVDPAFGFALGWNYWLNGAITIAVDLTTAGLITQFWFPHLPSWI 126 A ++P SGSF+ YG YV+ FGFALGWNYW N A+TIAVDL A L+ +WFP P W+ Sbjct: 73 AAFMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQLVMTYWFPDAPGWV 132 Query: 127 FSGIATVLIFIINVMAVGAFGETEYWLSTIKVITIVLFLAIGLLTIFGVLGQGNVDVVAN 186 +S + ++F++N ++V FGE EYW S IKV T+++F+ +G++ IFG+ +N Sbjct: 133 WSALFLGIMFLLNWISVKGFGEAEYWFSLIKVATVIIFIIVGVMMIFGIFKGAQPAGWSN 192 Query: 187 LTAGNHGFVGGISGFVGVLLIAGFSFQGTEMLGITAGESEDPGKTIPKAMNSIFWRILLF 246 + F GG + +GV +I GFSFQGTE++GI AGESE+P K IP+A+ +FWRILLF Sbjct: 193 WVIDDAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESENPEKNIPRAVRQVFWRILLF 252 Query: 247 YIFSIIVIAAIINFKDPRLL-NPSSTAVMSPFTIVFKNIGFAVAASVMNAVILTSVISSA 305 Y+F+I++I+ II + DP LL N +SPFT+VF++ G AA++MNAVILT+V+S+ Sbjct: 253 YVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSAAAIMNAVILTAVLSAG 312 Query: 306 NSVMYASTRILYSLGQEKGAPKFFGRTAKNGIPFYALLATTIICFIAFLTGIFGTQ-IYL 364 NS MYASTR+LY+L + AP+ F + +K G+P AL ATT+I + FL+ +FG Q +YL Sbjct: 313 NSGMYASTRMLYTLACDGKAPRIFSKLSKGGVPRNALYATTVIAGLCFLSSMFGNQTVYL 372 Query: 365 FLIDLSSLTGFLAWLGISVSHIRFRRAYIAQGKKLEDLPYKAKWFPFGPIVALLMTGAIA 424 +L++ S +TGF+AWLGI++SH RFRR Y+ QG L DLPY++ +FP GPI A ++ I Sbjct: 373 WLLNTSGMTGFIAWLGIAISHYRFRRGYVLQGNDLNDLPYRSGFFPLGPIFAFVLCLIIT 432 Query: 425 I--NLDPAMLFSEHWGEGLALYAAIPIFIVLYFGYKWKYNTKIIPLEEV 471 + N + + + WG A Y IP+F+V++FGYK T+ + E+ Sbjct: 433 LGQNYEAFLKDTIDWGGVAATYIGIPLFLVIWFGYKLAKGTRFVRYSEM 481 Lambda K H 0.327 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: 757 Number of extensions: 39 Number of successful extensions: 4 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: 477 Length of database: 489 Length adjustment: 34 Effective length of query: 443 Effective length of database: 455 Effective search space: 201565 Effective search space used: 201565 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 (21.7 bits) S2: 52 (24.6 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