Align ABC-type sugar transport system, ATP-binding protein; EC 3.6.3.17 (characterized, see rationale)
to candidate WP_086510989.1 BZY95_RS16555 L-arabinose ABC transporter ATP-binding protein AraG
Query= uniprot:A0A0C4Y5F6 (540 letters) >NCBI__GCF_002151265.1:WP_086510989.1 Length = 497 Score = 362 bits (929), Expect = e-104 Identities = 229/509 (44%), Positives = 303/509 (59%), Gaps = 19/509 (3%) Query: 12 PLLALRNICKTFPGVRALRKVELTAYAGEVHALMGENGAGKSTLMKILSGAYTADPGGEC 71 P L I FPGVRAL V A+AG+VHALMGENGAGKSTL+K+LSG G Sbjct: 4 PYLRFDGISMVFPGVRALDGVSFGAHAGQVHALMGENGAGKSTLLKVLSGVNHPSEGA-L 62 Query: 72 HIDGQRVQIDGPQSARDLGVAVIYQELSLAPNLSVAENIYLGRALQRRGLVARGDMVRAC 131 IDG+R + A G+A+IYQEL+L+PN++VAEN+ LG+ R G + R + Sbjct: 63 WIDGERHVFANAREALAQGIAIIYQELTLSPNMTVAENLLLGQLPTRHGFIKRRQLRERA 122 Query: 132 APTLARLG-ADFSPAANVASLSIAQRQLVEIARAVHFEARILVMDEPTTPLSTHETDRLF 190 LA LG D P+ V LSI Q+Q++EI RA+ ARI+ DEPT+ LS ET +L Sbjct: 123 LAILADLGEGDIHPSTKVRELSIGQQQMIEIGRALLRNARIIAFDEPTSSLSVQETRQLK 182 Query: 191 ALIRQLRGEGMAILYISHRMAEIDELADRVTVLRDGCFVGT-LDRAHLSQAALVKMMVGR 249 +I +LR EG +LY++HRM E+ ++ D VTV RDG + T A L LV MVGR Sbjct: 183 RIISRLREEGRVVLYVTHRMEEVFDMCDAVTVFRDGKHIRTHASLAALDHDTLVSEMVGR 242 Query: 250 DLSGFYTKTHGQAVEREVMLSVRDVADGRRVKG-CSFDLRAGEVLGLAGLVGAGRTELAR 308 D+ Y + + EV+L + D +GR +K SF++R GEV GL GLVGAGR+EL R Sbjct: 243 DIEDVYG--YRERERGEVILEI-DAIEGRGLKAPVSFEVRRGEVFGLFGLVGAGRSELMR 299 Query: 309 LVFGADARTRGEVRIANPAGSGGLVTLPAGGPRQAIDAGIAYLTEDRKLQGLFLDQSVHE 368 LV GA+ + GEVR A P +AI GIA EDRK QG+F SV + Sbjct: 300 LVCGAERASAGEVRFQGQARR-------FASPGEAIRMGIAMCPEDRKSQGIFPVASVAD 352 Query: 369 NINLIVAARDALGLGRLNRTAARRRTTEA-IDTLGIRVAHAQVNVGALSGGNQQKVMLSR 427 N+N I R G L T R EA I L I+ + +G LSGGNQQKV+L+R Sbjct: 353 NLN-ISCRRFFRRWGVLRDTRRERANAEAYIQRLSIKTPGPRTAIGTLSGGNQQKVILAR 411 Query: 428 LLEIQPRVLILDEPTRGVDIGAKSEIYRLINALAQSGVAILMISSELPEVVGLCDRVLVM 487 L + + ++DEPTRG+D+GA+ +IY L+ L + G ++++ISS+L EV +CDR+ VM Sbjct: 412 WLAEKIELFVVDEPTRGIDVGARRDIYTLLFDLTEQGKSVVVISSDLAEVSSICDRIGVM 471 Query: 488 REGTLAGEVRPAGSAAETQERIIALATGA 516 R+G L EV P A TQER++ LA A Sbjct: 472 RDGALV-EVVPRHEA--TQERLLGLALPA 497 Lambda K H 0.320 0.136 0.382 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: 625 Number of extensions: 37 Number of successful extensions: 10 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: 540 Length of database: 497 Length adjustment: 35 Effective length of query: 505 Effective length of database: 462 Effective search space: 233310 Effective search space used: 233310 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 Apr 09 2024. 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