Align Galactose/methyl galactoside import ATP-binding protein MglA aka B2149, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate WP_086510989.1 BZY95_RS16555 L-arabinose ABC transporter ATP-binding protein AraG
Query= TCDB::P0AAG8 (506 letters) >NCBI__GCF_002151265.1:WP_086510989.1 Length = 497 Score = 373 bits (958), Expect = e-108 Identities = 207/496 (41%), Positives = 306/496 (61%), Gaps = 8/496 (1%) Query: 11 EYLLEMSGINKSFPGVKALDNVNLKVRPHSIHALMGENGAGKSTLLKCLFGIYQKDSGTI 70 E L GI+ FPGV+ALD V+ +HALMGENGAGKSTLLK L G+ G + Sbjct: 3 EPYLRFDGISMVFPGVRALDGVSFGAHAGQVHALMGENGAGKSTLLKVLSGVNHPSEGAL 62 Query: 71 LFQGKEIDFHSAKEALENGISMVHQELNLVLQRSVMDNMWLGRYPTKGMFVDQDKMYRET 130 G+ F +A+EAL GI++++QEL L +V +N+ LG+ PT+ F+ + ++ Sbjct: 63 WIDGERHVFANAREALAQGIAIIYQELTLSPNMTVAENLLLGQLPTRHGFIKRRQLRERA 122 Query: 131 KAIFDEL-DIDIDPRARVGTLSVSQMQMIEIAKAFSYNAKIVIMDEPTSSLTEKEVNHLF 189 AI +L + DI P +V LS+ Q QMIEI +A NA+I+ DEPTSSL+ +E L Sbjct: 123 LAILADLGEGDIHPSTKVRELSIGQQQMIEIGRALLRNARIIAFDEPTSSLSVQETRQLK 182 Query: 190 TIIRKLKERGCGIVYISHKMEEIFQLCDEVTVLRDGQWIATEP-LAGLTMDKIIAMMVGR 248 II +L+E G ++Y++H+MEE+F +CD VTV RDG+ I T LA L D +++ MVGR Sbjct: 183 RIISRLREEGRVVLYVTHRMEEVFDMCDAVTVFRDGKHIRTHASLAALDHDTLVSEMVGR 242 Query: 249 SLNQRFPDKENKPGEVILEVRNLTS--LRQPSIRDVSFDLHKGEILGIAGLVGAKRTDIV 306 + + +E + GEVILE+ + L+ P VSF++ +GE+ G+ GLVGA R++++ Sbjct: 243 DIEDVYGYRERERGEVILEIDAIEGRGLKAP----VSFEVRRGEVFGLFGLVGAGRSELM 298 Query: 307 ETLFGIREKSAGTITLHGKQINNHNANEAINHGFALVTEERRSTGIYAYLDIGFNSLISN 366 + G SAG + G+ + EAI G A+ E+R+S GI+ + N IS Sbjct: 299 RLVCGAERASAGEVRFQGQARRFASPGEAIRMGIAMCPEDRKSQGIFPVASVADNLNISC 358 Query: 367 IRNYKNKVGLLDNSRMKSDTQWVIDSMRVKTPGHRTQIGSLSGGNQQKVIIGRWLLTQPE 426 R ++ L D R +++ + I + +KTPG RT IG+LSGGNQQKVI+ RWL + E Sbjct: 359 RRFFRRWGVLRDTRRERANAEAYIQRLSIKTPGPRTAIGTLSGGNQQKVILARWLAEKIE 418 Query: 427 ILMLDEPTRGIDVGAKFEIYQLIAELAKKGKGIIIISSEMPELLGITDRILVMSNGLVSG 486 + ++DEPTRGIDVGA+ +IY L+ +L ++GK +++ISS++ E+ I DRI VM +G + Sbjct: 419 LFVVDEPTRGIDVGARRDIYTLLFDLTEQGKSVVVISSDLAEVSSICDRIGVMRDGALVE 478 Query: 487 IVDTKTTTQNEILRLA 502 +V TQ +L LA Sbjct: 479 VVPRHEATQERLLGLA 494 Lambda K H 0.318 0.136 0.384 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: 569 Number of extensions: 27 Number of successful extensions: 8 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: 506 Length of database: 497 Length adjustment: 34 Effective length of query: 472 Effective length of database: 463 Effective search space: 218536 Effective search space used: 218536 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: 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