Align m-Inositol ABC transporter, ATPase component (itaA) (characterized)
to candidate H281DRAFT_06298 H281DRAFT_06298 L-arabinose ABC transporter ATP-binding protein
Query= reanno::pseudo3_N2E3:AO353_21385 (521 letters) >FitnessBrowser__Burk376:H281DRAFT_06298 Length = 519 Score = 404 bits (1039), Expect = e-117 Identities = 210/490 (42%), Positives = 317/490 (64%), Gaps = 4/490 (0%) Query: 28 LEIINVSKGFPGVVALSDVQLRVRPGSVLALMGENGAGKSTLMKIIAGIYQPDAGELRLR 87 L N+ K FPGV AL V V G V LMGENGAGKSTL+KI+ G YQPD+G + + Sbjct: 12 LRFDNIGKVFPGVRALDGVSFDVNVGQVHGLMGENGAGKSTLLKILGGEYQPDSGRVMID 71 Query: 88 GKPVTFDTPLAALQAGIAMIHQELNLMPHMSIAENIWIGREQLNGFHMIDHREMHRCTAQ 147 GK V F + +++ AGIA+IHQEL +P +++AEN+ +G + N F ++ R+ R + Sbjct: 72 GKEVRFTSAASSIAAGIAVIHQELQYVPDLTVAENLLLG-QLPNSFGWVNKRDAKRFVRE 130 Query: 148 LLERLRINLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITDKEVAHLFSII 207 LE + + LDP ++ LSIA+RQMVEI KA+ ++ ++ +DEPTS+++ +E LF ++ Sbjct: 131 RLEAMGVALDPNAKLRKLSIAQRQMVEICKALLRNARVIALDEPTSSLSHRETEVLFKLV 190 Query: 208 ADLKAQGKGIIYITHKMNEVFSIADEVAVFRDGAYIGLQ-RADSMDGDSLISMMVGRELS 266 DL+A + +IYI+H+M+E++ + D +FRDG I + + D+++S MVGRE+S Sbjct: 191 RDLRADNRAMIYISHRMDEIYELCDACTIFRDGRKIASHPTLEGVSRDTIVSEMVGREIS 250 Query: 267 QLFPVREKPIGDLLMSVRDLRLDGVFKGVSFDLHAGEILGIAGLMGSGRTNVAEAIFGIT 326 ++ E+P+G++ + + + + + SF++ GEI+G GL+G+GR+ + ++G Sbjct: 251 DIYNYSERPLGEVRFAAKAIEGHALSQPASFEVRRGEIVGFFGLVGAGRSELMHLVYGTE 310 Query: 327 PSDGGEICLDGQPVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEMAVLPHYAGN 386 GGE+ LDG+ +R+ AI G L EDRK G+ +V EN+ ++ HY Sbjct: 311 HKKGGELVLDGKTIRVKSAGEAIRHGIVLCPEDRKEEGIVAMATVSENINISCRRHYLRA 370 Query: 387 G-FIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLM-TNPRILILDE 444 G F+ +K + K L++KTPS Q I LSGGNQQKA+L+RWL + +++ILDE Sbjct: 371 GVFLDRKKEAETADRFIKLLKIKTPSRRQKIRFLSGGNQQKAILSRWLAEPDLKVVILDE 430 Query: 445 PTRGIDVGAKAEIYRLISYLASEGMAVIMISSELPEVLGMSDRVMVMHEGDLMGTLDRSE 504 PTRGIDVGAK EIY +I LA G A++MISSELPEVLG+SDR++VM +G + G L R + Sbjct: 431 PTRGIDVGAKHEIYNVIYQLAERGCAIVMISSELPEVLGVSDRIVVMRQGRIAGELSRKD 490 Query: 505 ATQERVMQLA 514 AT++ V+ LA Sbjct: 491 ATEQAVLSLA 500 Lambda K H 0.321 0.137 0.391 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: 646 Number of extensions: 32 Number of successful extensions: 9 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: 521 Length of database: 519 Length adjustment: 35 Effective length of query: 486 Effective length of database: 484 Effective search space: 235224 Effective search space used: 235224 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: 52 (24.6 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:
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