Align Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate H281DRAFT_00166 H281DRAFT_00166 carbohydrate ABC transporter substrate-binding protein, CUT1 family
Query= uniprot:A0A165KPY4 (416 letters) >FitnessBrowser__Burk376:H281DRAFT_00166 Length = 415 Score = 438 bits (1126), Expect = e-127 Identities = 238/412 (57%), Positives = 284/412 (68%), Gaps = 8/412 (1%) Query: 8 AAVAVGLAAAMSA--SAGEVEVLHYWTSGGEAKSVAELKKIMQGKGHTWRDFAVAGGGGD 65 A A GL +SA +A VEVLH+WTSGGE+K+V LK M +G+TW+DFAVAGG G Sbjct: 9 ALCAAGLMCGVSAVQAAESVEVLHWWTSGGESKAVGVLKDDMTKQGYTWKDFAVAGGAGA 68 Query: 66 SAMTVLKSRVISGNPPSAAQTKGPAIQEWASEGVLANMDTLAKAEKWDELLPKVVADVMK 125 +AMT LK++VISGN PSAAQ KGP IQ+WAS+GVL +D++A W + LP + +M Sbjct: 69 AAMTALKTQVISGNAPSAAQIKGPLIQDWASQGVLVPIDSVAG--DWKKNLPPEIDKIMH 126 Query: 126 YKGAYVAAPVNVHRVNWMWGSSEALKKAGVAAMPKTWDEFFAAADKLKAAGLVPVAHGGQ 185 G YVAAP +VHRVNW++ + AL KAG +P TW EFFA ADK+KAAG+ P+A GGQ Sbjct: 127 ADGHYVAAPFSVHRVNWLYINKAALDKAG-GKVPTTWPEFFAVADKMKAAGIQPIAMGGQ 185 Query: 186 NWQDFTTFESVVLGVGGAKFYQDALVKLDNTALTSDTMKKSLETFRRIKGYTDPGAPGRD 245 WQD T +E VVL G A FY+ ALV LD LTSD M +T R+I+GY D G GRD Sbjct: 186 PWQDLTLWEDVVLSQG-ADFYKKALVDLDEKTLTSDKMVGVFDTVRKIQGYFDAGRTGRD 244 Query: 246 WNLATAMLIQGKAGFQLMGDWAKGEFLAAGKAPGKDFLCAAAPGSANAFTFNVDSFILFK 305 WNLATAM+I GKAG Q MGDWAKGEF AGK G D++CAA PG+ A+TFNVDSF+ F+ Sbjct: 245 WNLATAMVINGKAGMQFMGDWAKGEFANAGKKSGSDYVCAAVPGTEKAYTFNVDSFVFFQ 304 Query: 306 LK-DAAAQKAQSDLASSIMSPAFQEVFNLNKGSIPVRAGQPMDKFDDCAKASAKDFVDTA 364 K AA Q LA +IMSP FQE F+LNKGSIPVR G M KFDDCAK S D Sbjct: 305 QKGQKAATPGQLALAKTIMSPEFQEQFSLNKGSIPVRLGVSMAKFDDCAKKSYADEQVAI 364 Query: 365 KSGGLVPSAAHGMAIAPATEGAIKDVVSQFWNDDKVSVADAMKKIAAAAKTK 416 KSGG VPS AHGMA A GAI DVV++F N + S A+ +A AAKTK Sbjct: 365 KSGGYVPSLAHGMAQPDAAAGAISDVVTKFMNSQQDS-KSAVAALAKAAKTK 415 Lambda K H 0.315 0.128 0.383 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: 40 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 416 Length of database: 415 Length adjustment: 31 Effective length of query: 385 Effective length of database: 384 Effective search space: 147840 Effective search space used: 147840 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 50 (23.9 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