Align glucose transporter, permease component (characterized)
to candidate SM_b20903 SM_b20903 sugar uptake ABC transporter permease
Query= reanno::Phaeo:GFF3640 (433 letters) >FitnessBrowser__Smeli:SM_b20903 Length = 453 Score = 461 bits (1186), Expect = e-134 Identities = 231/424 (54%), Positives = 306/424 (72%), Gaps = 8/424 (1%) Query: 11 EHSKRGLFQQLELDVRLLGMIGAFVILCIGFNILT----DGRFLTPRNIFNLTIQTVSVA 66 E+ + F+ E+D RLLGM+GA +I+ +GF ++T DG FL PRN++NLT+QT SVA Sbjct: 30 ENPVKRFFRATEIDTRLLGMVGALIIIWLGFQVMTGGLFDGLFLKPRNLWNLTVQTSSVA 89 Query: 67 IMATGMVFVIVTRHIDLSVGALLATCSAVMAVVQTDVLPDMFGLGLNHPATWIITVAVGL 126 +MATGMV VIVTR+IDLSVG++L C +M V+Q VLP GLG HPATW IT+A G+ Sbjct: 90 VMATGMVLVIVTRNIDLSVGSVLGFCGMIMGVLQAQVLPQYLGLG--HPATWAITLACGI 147 Query: 127 AIGTLIGAFQGWMVGFLTIPAFIVTLGGFLVWRNVAWYLTDGQTIGPLDSTF-LVFGGTS 185 A+G IGA G ++ FL +PAFIVTLGG LVWR W++T GQT+ P+D+TF L+ GGT Sbjct: 148 AVGGAIGALHGSIIAFLNVPAFIVTLGGLLVWRGATWFVTSGQTVAPMDATFRLMGGGTE 207 Query: 186 GTLGTTLSWVVGIVATLLALAALWNSRRAKQGHGFPVKPAWAEAVIAGSIAASILGFVAI 245 G++G T SW+VG +A + + A+ NSR+ ++ GFP++P WAE ++ A +LG VA+ Sbjct: 208 GSIGATASWIVGSLACIAIVGAILNSRKQRKRFGFPLRPVWAEYFLSILGCALVLGAVAV 267 Query: 246 LNAYQIPARRLKRMMEAQGETMPEG-LVVGYGLPISVLILIATAVVMTIIARRTRLGRYI 304 N Y P +R +A G P+G L + +G+ I VL+ I +VMT IA R R GRY+ Sbjct: 268 ANHYYWPVNIARRYADANGIAWPDGGLQISHGIAIPVLVAIVVGIVMTFIATRLRFGRYV 327 Query: 305 FATGGNPDAAELSGINTRLLTVKIFALMGFLCALSAVVASARLANHSNDIGTLDELRVIA 364 FA GGNP+AAEL+GI TR +TVKIF LMG LCA++A +++ARL +N G LDEL IA Sbjct: 328 FALGGNPEAAELAGIKTRWVTVKIFTLMGVLCAIAAAISTARLNAATNAQGELDELYTIA 387 Query: 365 AAVIGGTALSGGFGTIYGAILGALIMQSLQSGMAMVGVDAPFQNIVVGTVLVAAVWIDIL 424 AAVIGGT+L+GG GTI GA++GAL+MQSLQSGM ++G+D PFQ IVVG VLV AVW+D + Sbjct: 388 AAVIGGTSLAGGVGTIAGAMIGALVMQSLQSGMVLLGIDTPFQRIVVGVVLVTAVWLDTV 447 Query: 425 YRKR 428 YR R Sbjct: 448 YRAR 451 Lambda K H 0.327 0.141 0.419 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: 722 Number of extensions: 41 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: 433 Length of database: 453 Length adjustment: 32 Effective length of query: 401 Effective length of database: 421 Effective search space: 168821 Effective search space used: 168821 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