Align D-galacturonate transporter (MFS superfamily) (characterized)
to candidate BWI76_RS16940 BWI76_RS16940 MFS transporter
Query= reanno::WCS417:GFF828 (454 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS16940 BWI76_RS16940 MFS transporter Length = 439 Score = 372 bits (955), Expect = e-107 Identities = 184/434 (42%), Positives = 270/434 (62%), Gaps = 12/434 (2%) Query: 5 KPTHVRYLILLMLFLVTTINYADRATIAIAGSSLQKDLGIDAVTLGYIFSAFGWAYVAGQ 64 +P+ R IL +L + T INY DR + IA L +LGIDA +G +FSAF W Y Q Sbjct: 18 RPSRRRIGILALLAVGTMINYLDRTVLGIAAPQLTAELGIDAAMMGIVFSAFAWTYALAQ 77 Query: 65 IPGGWLLDRFGSKKVYALSIFTWSLFTVLQGYVGEFGVSTAVVALFMLRFMVGLAEAPSF 124 IPGG LDRFG+K Y L++ WSLFT+ G ++ + +L + RF +G++EAP F Sbjct: 78 IPGGIFLDRFGNKVTYFLALTLWSLFTLFHG------MAVGLKSLLLCRFGLGVSEAPCF 131 Query: 125 PGNARIVAAWFPTAERGTASAIFNSAQYFATVLFAPLMGWIVYSFGWQHVFIVMGVIGII 184 P N+R+V+AWFP ER A+A++ +Y FAPL+ WI+ SFGW+ +FI +G G++ Sbjct: 132 PVNSRVVSAWFPQQERAKATAVYTVGEYLGLACFAPLLFWIMGSFGWRALFISVGAAGVL 191 Query: 185 FSLIWLKVIHSPRQHPMINEAEFNHIAANGAMVDMDQDKGKGKKTDGPKWDYIRQLLTNR 244 F+L+W + P + +N+ E HI G M G + T W +RQLL R Sbjct: 192 FALVWWRCYREPHEDKHLNQLEREHIINGGGM-----STGAEQHT-AFSWPLVRQLLAKR 245 Query: 245 MMLGVYLGQYCINGITYFFLTWFPVYLVQDRGMTILKAGFIASLPAICGFIGGVLGGVIS 304 +LG +GQ+ N + FFLTWFP YL +R M +K GF A +P + G + GG +S Sbjct: 246 QILGASIGQFAGNTVLVFFLTWFPTYLATERHMPWIKVGFFAIMPFLAAAGGVMFGGWVS 305 Query: 305 DYLLRKGHSLTFARKAPIIGGLLISSSIVACNYVDIEWMVVGFMALAFFGKGVGALGWAV 364 D LL+ S RK PII GLL++S+I+A N++ + V+ M+ AFFG+G+ LGW + Sbjct: 306 DKLLKATGSANLGRKLPIIAGLLMASTIIAANWLTSDLAVILVMSFAFFGQGMVGLGWTL 365 Query: 365 VSDTSPKQIAGLSGGLFNTFGNLASITTPIVIGYIISTTGSFKWALVFVGANALVAVFSY 424 +SD +PK + GL+GGLFN NLA I TP++IG+I++ +G+F +AL+++G AL+ V +Y Sbjct: 366 ISDIAPKGLGGLTGGLFNFCANLAGILTPLIIGFIVAASGNFFYALIYIGGAALLGVAAY 425 Query: 425 LVIVGPIKRVVLKE 438 L I+G +KR+ L + Sbjct: 426 LFILGDVKRIELSQ 439 Lambda K H 0.327 0.142 0.444 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: 654 Number of extensions: 39 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: 454 Length of database: 439 Length adjustment: 33 Effective length of query: 421 Effective length of database: 406 Effective search space: 170926 Effective search space used: 170926 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 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