Align Xylose/arabinose import ATP-binding protein XylG; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_017221119.1 A923_RS0107850 ribose ABC transporter ATP-binding protein RbsA
Query= uniprot:P0DTT6 (251 letters) >NCBI__GCF_000276805.1:WP_017221119.1 Length = 501 Score = 159 bits (402), Expect = 1e-43 Identities = 86/243 (35%), Positives = 148/243 (60%), Gaps = 2/243 (0%) Query: 4 LLEIRDVHKSFGAVKALDGVSMEINKGEVVALLGDNGAGKSTLIKIISGYHKPDRGDLVF 63 +L++ + KSF VKALD + + G+V+ALLG+NGAGKSTL+K+++G + D+G + + Sbjct: 5 ILKLSGIEKSFPGVKALDNACLNVYPGKVMALLGENGAGKSTLMKVLTGIYHMDKGSINY 64 Query: 64 EGKKVIFNSPNDARSLGIETIYQDLALIPDLPIYYNIFLAREVTNKI-FLNKKKMMEESK 122 +G V F+ P ++ +GI I+Q+L LIP+L I NI+L RE TN + +M ++ Sbjct: 65 QGSDVTFDGPRHSQEVGISIIHQELNLIPELTIAENIYLGRETTNAFGGIKWTQMFADAD 124 Query: 123 KLLDSLQIRIPDINMKVENLSGGQRQAVAVARAVYFSAKMILMDEPTAALSVVEARKVLE 182 LL L ++ + E LS G++Q V +A+A+ F +++I+MDEPT AL+ E + + + Sbjct: 125 ALLQRLNVKHSSRQLLGE-LSLGEQQMVEIAKALSFKSQVIVMDEPTDALTESETKSLFK 183 Query: 183 LARNLKKKGLGVLIITHNIIQGYEVADRIYVLDRGKIIFHKKKEETNVEEITEVMTSFAL 242 + L+ +G G++ I+H + + +E+ D I VL GK I + + + + E M L Sbjct: 184 VINELRNEGCGIVYISHRLKEIFEICDDITVLRDGKFIAEIAVTDIDEDGLIEKMVGRRL 243 Query: 243 GKV 245 ++ Sbjct: 244 DEI 246 Score = 90.9 bits (224), Expect = 5e-23 Identities = 56/216 (25%), Positives = 111/216 (51%), Gaps = 5/216 (2%) Query: 23 VSMEINKGEVVALLGDNGAGKSTLIKIISGYHKPDRGDLVFEGKKVIFNSPNDARSLGIE 82 VS ++ GE++ + G GAG++ L+K I G GD++ + K V +P D + GI Sbjct: 272 VSFTLDHGEILGISGLMGAGRTELMKAIYGALPRQSGDVILDDKVVSPITPRDGLANGIA 331 Query: 83 TIYQDL---ALIPDLPIYYNIFLAR--EVTNKIFLNKKKMMEESKKLLDSLQIRIPDINM 137 I +D LI L + N+ L ++ + L+ K + + ++ P + Sbjct: 332 YISEDRKGDGLILGLSVKENMSLCALDALSKGLQLDHAKEATAVEDFMRQFNVKTPSRDQ 391 Query: 138 KVENLSGGQRQAVAVARAVYFSAKMILMDEPTAALSVVEARKVLELARNLKKKGLGVLII 197 + NLSGG +Q VA+A+ + K++++DEPT + V +++ +L K +G+ ++++ Sbjct: 392 IIGNLSGGNQQKVAIAKGLMTRPKVLILDEPTRGVDVGAKKEIYQLINQFKAEGMSIILV 451 Query: 198 THNIIQGYEVADRIYVLDRGKIIFHKKKEETNVEEI 233 + + + ++DRI V+ G+I + N E++ Sbjct: 452 SSEMPEVLGMSDRILVMHEGRISGEFMAADANQEKL 487 Lambda K H 0.318 0.137 0.371 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: 275 Number of extensions: 10 Number of successful extensions: 4 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: 501 Length adjustment: 29 Effective length of query: 222 Effective length of database: 472 Effective search space: 104784 Effective search space used: 104784 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: 49 (23.5 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