Align polyol transporter 5 (characterized)
to candidate Ga0059261_1777 Ga0059261_1777 MFS transporter, sugar porter (SP) family
Query= CharProtDB::CH_091483 (539 letters) >lcl|FitnessBrowser__Korea:Ga0059261_1777 Ga0059261_1777 MFS transporter, sugar porter (SP) family Length = 458 Score = 218 bits (556), Expect = 3e-61 Identities = 146/459 (31%), Positives = 236/459 (51%), Gaps = 41/459 (8%) Query: 43 ASMTSILLGYDIGVMSGAMIYIKRDLKINDLQIGILAGSLNIYSLIGSCAAGRTSDWIGR 102 A++ +L G+D V+SGA ++ + D +G S I +++GS AG +D GR Sbjct: 29 AALGGLLFGFDTAVISGATQALQLQFGLTDAMLGFTVASALIGTVLGSLIAGAPADRFGR 88 Query: 103 RYTIVLAGAIFFAGAILMGLSPNY-AFLMFGRFIAGIGVGYALMIAPVYTAEVSPASSRG 161 + ++ + ++ GL+P+ AFL+F RF+ G+ +G A ++ P+Y AEVSPA RG Sbjct: 89 KGVMLTVAIAYVVSSLGTGLAPDLNAFLVF-RFMGGLAIGAASVVTPIYIAEVSPARFRG 147 Query: 162 FLNSFPEVFINAGIMLGYVSNLAFSNL-PLKVGWRLMLGIGAVPSVILAIGVLAMPESPR 220 L + ++ I GI++ ++SN + L V WR M GI AVPS I + L +PESPR Sbjct: 148 RLVAMNQLNIVLGILIAFLSNYIIAGLVQYDVAWRWMFGIVAVPSTIFLLVTLLLPESPR 207 Query: 221 WLVMQGRLGDAKRVLDKTSDSPTEATLR----LEDIKHAAGIPADCHDDVVQVSRRNSHG 276 WL + G+ A+ V+ + + A L E + AAG P ++ +R+ Sbjct: 208 WLAIHGQADRARDVMQRLGFADPRAELARIELAEAREEAAGKP--------RLFQRSHF- 258 Query: 277 EGVWRELLIRPTPAVRRVMIAAIGIHFFQQASGIDAVVLFSPRIFKTAGLKTDHQQLLAT 336 TP + AI I F Q SGI+A++ ++PRIF+ AG D LL + Sbjct: 259 -----------TP-----VACAIAIAMFNQLSGINALLYYAPRIFELAGAGAD-SALLQS 301 Query: 337 VAVGVVKTSFILVATFLLDRIGRRPLLLTSVGGMVLSLAALGTSLTIIDQSEKKVMWAVV 396 +AVG F + A FL+DR GRRPLL +L +G L +++ Sbjct: 302 IAVGGTNLVFTVAALFLIDRFGRRPLLFVGSVICAATLLLVGWQLESAKPDGTLILFG-- 359 Query: 397 VAIATVMTYVATFSIGAGPITWVYSSEIFPLRLRSQGSSMGVVVNRVTSGVISISFLPMS 456 ++ ++A F++ G + WV+ SE+FP +R +G ++G + V + I+ +F P+ Sbjct: 360 -----LLGFIAAFAMSQGAVIWVFISEVFPSAVRGKGQALGSTTHWVMAAAITWAF-PVF 413 Query: 457 KAMTTGGAFYLFGGIATVAWVFFYTFLPETQGRMLEDMD 495 A G F FG + + ++ + F+PET G LEDM+ Sbjct: 414 AASVGGWVFAFFGAMMLLQLLWTWKFMPETNGIALEDMN 452 Lambda K H 0.322 0.137 0.410 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: 32 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: 539 Length of database: 458 Length adjustment: 34 Effective length of query: 505 Effective length of database: 424 Effective search space: 214120 Effective search space used: 214120 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.9 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 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