Align D-fructose transporter, sugar porter family (characterized)
to candidate Echvi_2805 Echvi_2805 MFS transporter, sugar porter (SP) family
Query= reanno::Korea:Ga0059261_1777 (458 letters) >FitnessBrowser__Cola:Echvi_2805 Length = 448 Score = 383 bits (984), Expect = e-111 Identities = 202/436 (46%), Positives = 289/436 (66%), Gaps = 10/436 (2%) Query: 22 IILSAAGAALGGLLFGFDTAVISGATQALQLQFGLTDAMLGFTVASALIGTVLGSLIAGA 81 +I + AALGG LFGFDTAVISGA + +Q ++ L+D G VA AL GTV+G+L G Sbjct: 7 VIFLSIVAALGGFLFGFDTAVISGAERFIQEKWQLSDWTHGMAVAIALYGTVIGALFGGI 66 Query: 82 PADRFGRKGVMLTVAIAYVVSSLGTGLAPDLNAFLVFRFMGGLAIGAASVVTPIYIAEVS 141 PAD++GRK +L + + Y +S+LG+ LAPD+ +F+ FRF+GGL +GA+SVV P+YI+E++ Sbjct: 67 PADKYGRKTSLLWIGVLYFISALGSALAPDVYSFMFFRFIGGLGVGASSVVAPMYISEIA 126 Query: 142 PARFRGRLVAMNQLNIVLGILIAFLSNYIIAGLVQYDVAWRWMFGIVAVPSTIFLLVTLL 201 PA+ RG LVA+ Q NIV GIL+A+ SNY+I + + +WRWM G+ A+P+ I+ L+++ Sbjct: 127 PAKNRGVLVALYQFNIVFGILMAYFSNYLIE-MADLNESWRWMMGMEAIPALIYTLLSIR 185 Query: 202 LPESPRWL-AIHGQADRARDVMQRLGFADPRA--ELARIELAEAREE--AAGKPRLFQRS 256 +P+SPRWL A H + + A ++++ DP E + + E E G LF+ S Sbjct: 186 VPKSPRWLIAHHNKVEEATQILRK---TDPEGVDEAIHLAIEERNREKIKVGFAVLFKHS 242 Query: 257 HFTPVACAIAIAMFNQLSGINALLYYAPRIFELAGAGADSALLQSIAVGGTNLVFTVAAL 316 H AI IA+FNQLSGINA++Y+APR+FE+AG SALL +I +G N++ T+ L Sbjct: 243 HLKTTLLAIMIALFNQLSGINAIIYFAPRVFEMAGIDQKSALLSTIGIGVVNMIATMIGL 302 Query: 317 FLIDRFGRRPLLFVGSVICAATLLLVGWQLESAKPDGTLILFGLLGFIAAFAMSQGAVIW 376 +LIDR GR+ L+ +GS+ +LLL+ + + + + FIA+ A+ QG+VIW Sbjct: 303 YLIDRIGRKKLMVIGSIGYIISLLLMAYSFSGGVINSGYLPLFVFVFIASHAVGQGSVIW 362 Query: 377 VFISEVFPSAVRGKGQALGSTTHWVMAAAITWAFPVFAASVG-GWVFAFFGAMMLLQLLW 435 VFISEVFP+ R GQ++G THW++AA I FP FA S G +F FF MM LQLLW Sbjct: 363 VFISEVFPNETRAFGQSIGCFTHWILAAVIANVFPFFANSFGPASIFGFFAVMMGLQLLW 422 Query: 436 TWKFMPETNGIALEDM 451 MPET G +LE++ Sbjct: 423 VLTKMPETKGRSLEEI 438 Lambda K H 0.327 0.139 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: 616 Number of extensions: 34 Number of successful extensions: 5 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: 458 Length of database: 448 Length adjustment: 33 Effective length of query: 425 Effective length of database: 415 Effective search space: 176375 Effective search space used: 176375 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