Align Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate BPHYT_RS04180 BPHYT_RS04180 sugar ABC transporter substrate-binding protein
Query= uniprot:A0A165KPY4 (416 letters) >FitnessBrowser__BFirm:BPHYT_RS04180 Length = 415 Score = 410 bits (1055), Expect = e-119 Identities = 218/411 (53%), Positives = 274/411 (66%), Gaps = 6/411 (1%) Query: 7 IAAVAVGLAAAMSASAGEVEVLHYWTSGGEAKSVAELKKIMQGKGHTWRDFAVAGGGGDS 66 I A + +A ++++A + VLH+WTSGGE+K++ LK M +G+ W+DFAVAGG G + Sbjct: 10 IVASTLATSAQVASAAESLSVLHWWTSGGESKAIRVLKDDMDKQGYEWKDFAVAGGAGAA 69 Query: 67 AMTVLKSRVISGNPPSAAQTKGPAIQEWASEGVLANMDTLAKAEKWDELLPKVVADVMKY 126 AMT LK++V+SGN PSAAQ KGP IQ+WA +GVL ++D A W LP + M Sbjct: 70 AMTALKTQVMSGNAPSAAQIKGPLIQDWADQGVLVDIDK--SATDWKAQLPAQINKTMMS 127 Query: 127 KGAYVAAPVNVHRVNWMWGSSEALKKAGVAAMPKTWDEFFAAADKLKAAGLVPVAHGGQN 186 KG YVAAP +VHR+NW+W + AL K G P TW EFFA ADK +AAG+ PVA GGQ Sbjct: 128 KGHYVAAPFSVHRINWLWINKAALDKVG-GKPPTTWPEFFALADKFRAAGITPVARGGQP 186 Query: 187 WQDFTTFESVVLGVGGAKFYQDALVKLDNTALTSDTMKKSLETFRRIKGYTDPGAPGRDW 246 WQD T +E+VVL G A FY+ A++ LD LTS M + +T R+I+GY D G+ GRDW Sbjct: 187 WQDMTIWETVVLSQG-ADFYRKAMIDLDQKTLTSPQMLQVFQTARKIQGYFDKGSTGRDW 245 Query: 247 NLATAMLIQGKAGFQLMGDWAKGEFLAAGKAPGKDFLCAAAPGSANAFTFNVDSFILFKL 306 NLATAM+I G G Q MGDWAKGEF A K D++CAAAPG++NAFT+ VDSF+ F+ Sbjct: 246 NLATAMVINGSGGMQFMGDWAKGEFANANKKADVDYICAAAPGTSNAFTYTVDSFVFFQQ 305 Query: 307 K-DAAAQKAQSDLASSIMSPAFQEVFNLNKGSIPVRAGQPMDKFDDCAKASAKDFVDTAK 365 A Q LA +IMSPAFQE F+L KGSIPVR MDKFD CAK S D T K Sbjct: 306 NGKKEATLGQLALAKTIMSPAFQEQFSLYKGSIPVRQDVSMDKFDACAKKSYADEQTTIK 365 Query: 366 SGGLVPSAAHGMAIAPATEGAIKDVVSQFWNDDKVSVADAMKKIAAAAKTK 416 S PS A G + ATEGAI DVV+ F N ++ +AM+K+AAAAK K Sbjct: 366 SNTFFPSFAFGDVQSSATEGAITDVVTGFMNSNE-DPQEAMRKVAAAAKVK 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: 564 Number of extensions: 32 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: 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