Align Glucose/galactose porter (characterized)
to candidate 7025147 Shewana3_2310 glucose/galactose transporter (RefSeq)
Query= TCDB::P0C105 (412 letters) >lcl|FitnessBrowser__ANA3:7025147 Shewana3_2310 glucose/galactose transporter (RefSeq) Length = 423 Score = 550 bits (1416), Expect = e-161 Identities = 281/424 (66%), Positives = 335/424 (79%), Gaps = 15/424 (3%) Query: 1 MATSIPTNNPLHTETSSQK---NYGFALTSLTLLFFMWGFITCLNDILIPHLKNVFQLNY 57 MA+SI T++ HT + S+ NY FAL SLT LFFMWGFITCLNDILIPHLK VF LNY Sbjct: 1 MASSINTSS--HTSSVSEAGNGNYRFALVSLTSLFFMWGFITCLNDILIPHLKAVFSLNY 58 Query: 58 TQSMLIQFCFFGAYFIVSLPAGQLVKRISYKRGIVVGLIVAAIGCALFIPAASYRVYALF 117 TQ+MLIQFCFFGAYF+VS+PAGQLVKR+ Y++GIV GL++A+IGC LF PAAS+ Y LF Sbjct: 59 TQAMLIQFCFFGAYFLVSIPAGQLVKRLGYQKGIVTGLVIASIGCGLFYPAASFATYGLF 118 Query: 118 LGALFVLASGVTILQVAANPYVTILGKPETAASRLTLTQAFNSLGTTVAPVFGAVLILSA 177 LGALFVLASG+TILQVAANPYV LG ETA+SRL LTQAFN+LGTTVAP FG++LILS Sbjct: 119 LGALFVLASGITILQVAANPYVNALGSSETASSRLNLTQAFNALGTTVAPFFGSILILSV 178 Query: 178 ATD-----ATVNAEADAVRFPYLLLALAFTVLAIIFAILKPPDVQEDEPALSDKKEG--- 229 A A NAEA+ V+ PYLLLA A VLAIIFA L P ++E A +++ + Sbjct: 179 AASVSSELAQANAEAEVVKLPYLLLAAALAVLAIIFAKLDLPVIREHSQAAAEEVQTHLG 238 Query: 230 --SAWQYRHLVLGAIGIFVYVGAEVSVGSFLVNFLSDPTVAGLSETDAAHHVAYFWGGAM 287 SA Q HLVLGA+GIFVYVGAEVS+GSFLVNFL + + G+ E AAH++AY+WGGAM Sbjct: 239 KTSALQSMHLVLGAVGIFVYVGAEVSIGSFLVNFLGEAHIVGMPEEQAAHYIAYYWGGAM 298 Query: 288 VGRFIGSAAMRYIDDGKALAFNAFVAIILLFITVATTGHIAMWSVLAIGLFNSIMFPTIF 347 VGRFIGSA M+ I G LAFNAF+A +L+ + + T+G +AMW++L +GLFNSIMFPTIF Sbjct: 299 VGRFIGSAVMQKIPAGTVLAFNAFMAALLVLVAMTTSGSVAMWAILGVGLFNSIMFPTIF 358 Query: 348 SLALHGLGSHTSQGSGILCLAIVGGAIVPLIQGALADAIGIHLAFLMPIICYAYIAFYGL 407 SLAL LG HTSQGSGILCLAIVGGAIVPL+QG LAD +GI LAF++P++CY +I FYG Sbjct: 359 SLALRDLGPHTSQGSGILCLAIVGGAIVPLLQGVLADNLGIQLAFILPVVCYGFILFYGA 418 Query: 408 IGSK 411 GSK Sbjct: 419 KGSK 422 Lambda K H 0.328 0.141 0.420 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: 698 Number of extensions: 30 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: 412 Length of database: 423 Length adjustment: 32 Effective length of query: 380 Effective length of database: 391 Effective search space: 148580 Effective search space used: 148580 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: 50 (23.9 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 preprint 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