Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate GFF2276 PGA1_c23080 ribose transport system permease protein RbsC
Query= uniprot:B2T9V8 (351 letters) >FitnessBrowser__Phaeo:GFF2276 Length = 324 Score = 131 bits (329), Expect = 3e-35 Identities = 96/310 (30%), Positives = 156/310 (50%), Gaps = 29/310 (9%) Query: 38 LRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLIVLTGKFDLSL 97 L + +L A AL I+ +P FLT N +V+ +SA L ++ L + +V++G DLS+ Sbjct: 13 LAKQGILIAFALFIIGFTIANPKFLTLDNFENVVRSSAILGVMALGVTFVVISGNLDLSV 72 Query: 98 ESTVGIAPAV--------GAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFLVV 149 S + + V G L +PA A + +GA+IGF+ G+L Sbjct: 73 GSMMSFSTIVVLDLHDKLGPTLAIPAMFA-------------MTLCLGALIGFLVGYL-- 117 Query: 150 RLRLNAFIVTLAMLIVLRGMLVGATKGGTL--FDMPTSFFAL-ATTIVLGLPLSVWLAAA 206 +LN+ IVTL ML + G+ + + G + D ++FA+ +LG+ + + A Sbjct: 118 --KLNSLIVTLGMLSAIHGLTLTYSGGKNMDIADKEGTWFAIFGQGNILGIQTPILIFIA 175 Query: 207 AFAIAAFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGY 266 A+ +L GR +YA+GGN AA +GIR R+ + +++ ++ + GLI Sbjct: 176 LAALLGIILAKTPFGRKVYAVGGNGTAATFSGIRRARVVFLCYIMSALCVATAGLIQASR 235 Query: 267 VGAINANQGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFW 326 G G+ V AA ++GG SL GG GT+F + GVL+LG +QN L L + F Sbjct: 236 SMGSQNTVGQGLELEVLAAVILGGASLLGGSGTIFKTVIGVLILGFIQNGLLLVGL-DFS 294 Query: 327 IQAIYGAIIL 336 +Q + II+ Sbjct: 295 VQYVVTWIII 304 Score = 25.8 bits (55), Expect = 0.002 Identities = 28/84 (33%), Positives = 40/84 (47%), Gaps = 6/84 (7%) Query: 98 ESTVGIAPAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVI-GFI-NGFLVVRLRLNA 155 ++TVG G L + AA G +G + V+G +I GFI NG L+V L + Sbjct: 240 QNTVG----QGLELEVLAAVILGGASLLGGSGTIFKTVIGVLILGFIQNGLLLVGLDFSV 295 Query: 156 FIVTLAMLIVLRGMLVGATKGGTL 179 V ++I+L L A K G L Sbjct: 296 QYVVTWIIIILAVWLDIAAKRGKL 319 Lambda K H 0.326 0.140 0.397 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: 290 Number of extensions: 19 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: 2 Length of query: 351 Length of database: 324 Length adjustment: 28 Effective length of query: 323 Effective length of database: 296 Effective search space: 95608 Effective search space used: 95608 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 (21.6 bits) S2: 49 (23.5 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