Align Galactose-proton symporter; Galactose transporter (characterized)
to candidate BWI76_RS03110 BWI76_RS03110 MFS transporter
Query= SwissProt::P0AEP1 (464 letters) >FitnessBrowser__Koxy:BWI76_RS03110 Length = 499 Score = 284 bits (726), Expect = 5e-81 Identities = 168/447 (37%), Positives = 259/447 (57%), Gaps = 15/447 (3%) Query: 18 VCFLAALAGLLFGLDIGVIAGALPFIADEFQITSHTQEWVVSSMMFGAAVGAVGSGWLSF 77 V +A L GLLFG D GVI+GAL F+ E +T T V SS++FGAA GA+ SG L+ Sbjct: 28 VALIATLGGLLFGYDTGVISGALLFMGTELHLTPFTTGLVTSSLLFGAAFGALLSGNLAN 87 Query: 78 KLGRKKSLMIGAILFVAGSLFSAAAPNVEVLILSRVLLGLAVGVASYTAPLYLSEIAPEK 137 GRKK ++ A+LF G++ ++ AP+V +I R++LG+AVG A+ T P+Y++EIAP Sbjct: 88 AAGRKKIILWLAVLFAIGAIGTSMAPDVNWMIFFRLILGVAVGGAAATVPVYIAEIAPAN 147 Query: 138 IRGSMISMYQLMITIGILGAYLSDTAFSYT----GAWRWMLGVIIIPAILLLIGVFFLPD 193 RG ++++ +LMI G L AY+S+ F WRWML V +PA+LL G+ F+PD Sbjct: 148 KRGQLVTLQELMIVSGQLLAYISNATFHEVWGGESTWRWMLAVATLPAVLLWFGMMFMPD 207 Query: 194 SPRWFAAKRRFVDAERVLLRLRDTSAEAKRELDEIRESLQVKQS-GWALFKENSN--FRR 250 SPRW+A K R +A RVL R R + + EL EI E+L +++ G F E + Sbjct: 208 SPRWYAMKGRLAEARRVLERTRHKD-DVEWELLEITETLDEQRNLGKPRFSEIMTPWLFK 266 Query: 251 AVFLGVLLQVMQQFTGMNVIMYYAPKIFELAGYTNTTEQMWGTVIVGLTNVLATFIAIGL 310 +G+ + V+QQ TG+N IMYYAP + G T+ ++ T+ G+ +VL TF+ I + Sbjct: 267 LFMIGIGIAVIQQLTGVNTIMYYAPTVLTSVGMTDNA-ALFATIANGVVSVLMTFVGIWM 325 Query: 311 VDRWGRKPTLTLGFLVMAAGMGVLGTMMHIGIHSPSAQ------YFAIAMLLMFIVGFAM 364 + + GR+P +G A + +G + ++ + + Q Y +A +L+F+ Sbjct: 326 LGKIGRRPMTMIGQFGCTACLVFIGAVSYLLPETVNGQPDALRAYMVLAGMLLFLSFQQG 385 Query: 365 SAGPLIWVLCSEIQPLKGRDFGITCSTATNWIANMIVGATFLTMLNTLGNANTFWVYAAL 424 + P+ W+L SEI P + R + + + WIAN ++ F +L LG + TF+++A + Sbjct: 386 ALSPVTWLLMSEIFPTRLRGIFMGGAVFSMWIANFLISLFFPILLAWLGLSGTFFIFAGI 445 Query: 425 NVLFILLTLWLVPETKHVSLEHIERNL 451 V + + VPET+H SLE IE L Sbjct: 446 GVFGAIFVIKCVPETRHRSLEQIEHYL 472 Lambda K H 0.327 0.140 0.425 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: 694 Number of extensions: 42 Number of successful extensions: 7 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: 464 Length of database: 499 Length adjustment: 34 Effective length of query: 430 Effective length of database: 465 Effective search space: 199950 Effective search space used: 199950 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: 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