Align Glucose/fructose:H+ symporter, GlcP (characterized)
to candidate N515DRAFT_0382 N515DRAFT_0382 MFS transporter, sugar porter (SP) family
Query= TCDB::P15729 (468 letters) >FitnessBrowser__Dyella79:N515DRAFT_0382 Length = 472 Score = 486 bits (1250), Expect = e-142 Identities = 254/456 (55%), Positives = 332/456 (72%), Gaps = 6/456 (1%) Query: 17 VLLISGVAALGGFLFGFDTAVINGAVAALQKHFQTDSLLTGLSVSLALLGSALGAFGAGP 76 V+LI+ AALGGFLFGFDTAVINGAV A++ F + G +VS ALLGSALGA+ AGP Sbjct: 17 VVLIAAAAALGGFLFGFDTAVINGAVDAVRGSFGLGAGRIGFAVSCALLGSALGAWYAGP 76 Query: 77 IADRHGRIKTMILAAVLFTLSSIGSGLPFTIWDFIFWRVLGGIGVGAASVIAPAYIAEVS 136 +ADR GR++TM +AAVL +S++GSGL +WD + WR++GGIGVG ASVIAP YIAEVS Sbjct: 77 LADRWGRVRTMQVAAVLLAISALGSGLVAGVWDLVLWRLVGGIGVGVASVIAPTYIAEVS 136 Query: 137 PAHLRGRLGSLQQLAIVSGIFIALLSNWFIALMAGGSAQNPWLFGAAAWRWMFWTELIPA 196 PA +RGRLGSLQQLAIV GIF ALLS+ ++A AGG++Q WL G AWRWMF ++PA Sbjct: 137 PARVRGRLGSLQQLAIVLGIFAALLSDAWLAGTAGGASQKLWL-GLEAWRWMFLVAVVPA 195 Query: 197 LLYGVCAFLIPESPRYLVAQGQGEKAAAILWKV----EGGDVPSRIEEIQATVSLDHKPR 252 L+YG +PESPR+LVA+G+ ++A +L +V + + ++ +I ++ +++P Sbjct: 196 LIYGSLVLGVPESPRHLVAKGRMDEAKQVLRQVLDLQDEHALQHKLGDIAQSLRSEYRPG 255 Query: 253 FSDLLSRRGGLLPIVWIGMGLSALQQFVGINVIFYYSSVLWRSVGFTEEKSLLITVITGF 312 DL GLLP+VW+G+ LS QQFVGINVIFYYSS LW SVGF+E + I+V+T Sbjct: 256 LRDLRGSMAGLLPVVWVGILLSVFQQFVGINVIFYYSSTLWHSVGFSESDAFSISVVTSV 315 Query: 313 INILTTLVAIAFVDKFGRKPLLLMGSIGMTITLGILSVVFGGATVVNGQPTLTGAAGIIA 372 +N+L TLVAIA VD+ GRKPLL +GS GMT+TLG+++ F A +L G++A Sbjct: 316 VNVLVTLVAIALVDRIGRKPLLAIGSAGMTVTLGLMAWCFSQAAGSGAALSLPAPWGMVA 375 Query: 373 LVTANLYVFSFGFSWGPIVWVLLGEMFNNKIRAAALSVAAGVQWIANFIISTTFPPLLDT 432 LV AN YV FG SWGP+VWVLLGEMF N+IRA AL+VAA QW+ANFII+++FP L + Sbjct: 376 LVAANAYVVFFGLSWGPMVWVLLGEMFPNRIRAIALAVAAAAQWVANFIITSSFPALSE- 434 Query: 433 VGLGPAYGLYATSAAISIFFIWFFVKETKGKTLEQM 468 +GL AYG+YA A +S+ F+ V+ETKG LE+M Sbjct: 435 LGLSFAYGVYAFFALVSLVFVVKAVRETKGMELEEM 470 Lambda K H 0.325 0.140 0.430 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: 679 Number of extensions: 31 Number of successful extensions: 4 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: 468 Length of database: 472 Length adjustment: 33 Effective length of query: 435 Effective length of database: 439 Effective search space: 190965 Effective search space used: 190965 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 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