Align D-lactate transporter, ATP-binding component (characterized)
to candidate WP_015448341.1 R2APBS1_RS13570 ABC transporter ATP-binding protein
Query= reanno::Phaeo:GFF1248 (251 letters) >NCBI__GCF_000230695.2:WP_015448341.1 Length = 588 Score = 84.7 bits (208), Expect = 4e-21 Identities = 65/232 (28%), Positives = 118/232 (50%), Gaps = 18/232 (7%) Query: 6 VKNVGKRFGGLQALSDVNLSVRENTVHAIIGPNGAGKSTLLNCLVGKLIPDTGSVMFDGK 65 ++ V KRFG ++AL ++ ++R + ++GP+GAGK+TL+ + G L+PD GSV G Sbjct: 20 IERVDKRFGAIRALRKLSATIRYGRLTGLVGPDGAGKTTLMRIMTGLLVPDAGSVSLAGF 79 Query: 66 SVLGRAPYEINQMGISRVFQTPEIFGDLSVLENMMIPCFAKRDGAFEMNAISAVSGQRDI 125 V+ + + + Q ++ DLSV+ENM + +A+ G M+A D+ Sbjct: 80 DVV--KDNDAIHVASGYMPQRFGLYEDLSVMENMRL--YARLRG---MDA----DRHADL 128 Query: 126 LEKAEHMLEEMNMADKRHMNAASMSRGDKRRLEIGMCLSQEPRLLLLDEPTAGMARADTN 185 + +LE + A +S G K++L + L P++LLLDEP G+ D Sbjct: 129 FAE---LLEFTRLGPFTKRLAGKLSGGMKQKLGLACALMARPKVLLLDEPGVGV---DPV 182 Query: 186 NTIDLLKQIKSERDITIAIIEHDMHV-VFSLADRITVLAQGTPLVEDDPQNI 236 + DL + +++ D +A++ ++ + + +L QG L + PQ + Sbjct: 183 SRQDLWRMVQALTDEGMAVVWSTAYLDEAERCESVLLLNQGKLLFDGPPQTL 234 Score = 78.6 bits (192), Expect = 3e-19 Identities = 65/237 (27%), Positives = 104/237 (43%), Gaps = 28/237 (11%) Query: 7 KNVGKRFGGLQALSDVNLSVRENTVHAIIGPNGAGKSTLLNCLVGKLIPDTGS---VMFD 63 +N+ KRFG A V+ V + + ++GPNGAGKST L G L P TG V D Sbjct: 342 RNLTKRFGPFTATDSVSFEVHKGEIFGLLGPNGAGKSTTFKMLCGLLKPTTGEAHVVGLD 401 Query: 64 GKSVLGRAPYEINQMGISRVFQTPEIFGDLSVLENMMIPCFAKRDGAFEMNAISAVSGQR 123 + G A + M Q ++G LSV +N+ G +++ + Sbjct: 402 LRRATGAAKSRLGYMA-----QKFSLYGLLSVRQNLEFSA-----GVYQLEG-------Q 444 Query: 124 DILEKAEHMLEEMNMADKRHMNAASMSRGDKRRLEIGMCLSQEPRLLLLDEPTAG---MA 180 E+ E M+ ++ S+ G K+RL + L P +L LDEPT+G + Sbjct: 445 TRRERIEEMIATFDLGGWLSATPDSLPLGHKQRLALACSLMHRPPVLFLDEPTSGVDPIT 504 Query: 181 RADTNNTIDLLKQIKSERDITIAIIEHDMHVVFSLADRITVLAQGTPLVEDDPQNIK 237 R + I+ L + + +TI + H M DR+ +L++ + D P +K Sbjct: 505 RREFWTHINGL----ARKGVTIMVTTHFMDEA-EYCDRVAMLSRARLIALDTPDALK 556 Lambda K H 0.318 0.135 0.379 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: 330 Number of extensions: 21 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: 251 Length of database: 588 Length adjustment: 30 Effective length of query: 221 Effective length of database: 558 Effective search space: 123318 Effective search space used: 123318 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 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 24 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:
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