Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate Ga0059261_2556 Ga0059261_2556 ABC-type multidrug transport system, ATPase component
Query= reanno::acidovorax_3H11:Ac3H11_792 (358 letters) >FitnessBrowser__Korea:Ga0059261_2556 Length = 587 Score = 76.3 bits (186), Expect = 2e-18 Identities = 64/217 (29%), Positives = 104/217 (47%), Gaps = 8/217 (3%) Query: 17 QQDSDYALLPLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRAS 76 + D A+ L + G L+GP G GKTT++ +++GLL P+ GK+ + D+ AS Sbjct: 19 KNDEVVAIDDLSASIKTGIITGLVGPDGAGKTTLIRMIAGLLTPTRGKLTVN--DLEPAS 76 Query: 77 PQERNIAQVFQFPV---IYDTMTVAENLAFPLRNRKVPEGQIKQRVGVIAEMLEMSGQLN 133 + Q+ P +Y+ +TV ENL R V + + E ++ Sbjct: 77 QGDALRQQLGYMPQRFGLYEDLTVLENLTLYSDLRGVDPAKRADMFERMLEFTDLKRFTE 136 Query: 134 QRAAGLAADAKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHELKLTL 193 +RA L+ KQK+ L L+ D +L DEP +DP + +L + + + E K T+ Sbjct: 137 RRAGKLSGGMKQKLGLACTLL-GDPQVLLLDEPSVGVDPISRRELWKMVGDLAGEGK-TI 194 Query: 194 IYVTHDQVEALTFADQVVVMTRGKAVQVGSADALFER 230 I+ T EA +V+++ GK + GS D L ER Sbjct: 195 IWSTAYLDEA-ERCPEVILLDHGKPLYCGSPDELAER 230 Score = 72.4 bits (176), Expect = 3e-17 Identities = 54/205 (26%), Positives = 98/205 (47%), Gaps = 10/205 (4%) Query: 27 LKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRASPQERN----I 82 + + + G Y LLGP+G GK+T ++ GLLVPS G G + R+ R + Sbjct: 354 VSFDVKRGEIYGLLGPNGAGKSTTFKMLCGLLVPSSGDANVLGYSLKRSPGDARQRLGYM 413 Query: 83 AQVFQFPVIYDTMTVAENLAFPLRNRKVPEGQIKQRVGVIAEMLEMSGQLNQRAAGLAAD 142 AQ F +Y T++V +N+ F + ++R+ + + + L L Sbjct: 414 AQKFS---LYGTLSVRQNMEFFAGIYGLDGSDRRERIDAMIDAFALKPYLAMSPDALPLG 470 Query: 143 AKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHELKLTLIYVTHDQVE 202 KQ+++L ++ D A + DEP + +DP + + + + E +T++ TH E Sbjct: 471 FKQRLALACAIMH-DPAILFLDEPTSGVDPLTRREFWTHINGV-VEKGVTVMVTTHFMDE 528 Query: 203 ALTFADQVVVMTRGKAVQVGSADAL 227 A + D++ ++ RGK + G+ D L Sbjct: 529 A-EYCDRIGLIYRGKLIASGAPDDL 552 Lambda K H 0.320 0.136 0.395 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: 423 Number of extensions: 22 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 358 Length of database: 587 Length adjustment: 33 Effective length of query: 325 Effective length of database: 554 Effective search space: 180050 Effective search space used: 180050 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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