Align Xylose/arabinose import ATP-binding protein XylG; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_084935592.1 HA51_RS15895 sugar ABC transporter ATP-binding protein
Query= uniprot:P0DTT6 (251 letters) >NCBI__GCF_002095475.1:WP_084935592.1 Length = 501 Score = 164 bits (416), Expect = 2e-45 Identities = 81/234 (34%), Positives = 151/234 (64%), Gaps = 1/234 (0%) Query: 4 LLEIRDVHKSFGAVKALDGVSMEINKGEVVALLGDNGAGKSTLIKIISGYHKPDRGDLVF 63 +LE+R++ + FG+ AL GV + + GEV AL+G+NGAGKSTL+KI++G + G+++ Sbjct: 6 ILEMREITRRFGSFYALKGVDLTVWPGEVHALMGENGAGKSTLMKILAGAYTASSGEILI 65 Query: 64 EGKKVIFNSPNDARSLGIETIYQDLALIPDLPIYYNIFLAREVTNKIFLNKKKMMEESKK 123 +G+ P +A + GI IYQ++ L P+L + NIFL E+T + +++M EE++ Sbjct: 66 DGQPYAIKGPKEALAAGITLIYQEINLAPNLTVAENIFLGSEITRGGLVKRRQMAEEAQL 125 Query: 124 LLDSLQIRIPDINMKVENLSGGQRQAVAVARAVYFSAKMILMDEPTAALSVVEARKVLEL 183 +++ L + ++ V LS ++Q V +ARA++ ++++++MDEPTAALS E ++ L Sbjct: 126 VINRLGAQFSATDL-VSRLSIAEQQQVEIARALHRNSRILVMDEPTAALSNRETEQLFAL 184 Query: 184 ARNLKKKGLGVLIITHNIIQGYEVADRIYVLDRGKIIFHKKKEETNVEEITEVM 237 + L+ +G+ ++ I+H + + YE++DR+ VL G+ + +++ N E+ +M Sbjct: 185 IKRLRSEGMAIIYISHRMAEVYELSDRVSVLRDGQYVGSLTRDQLNASELVRMM 238 Score = 114 bits (284), Expect = 5e-30 Identities = 71/243 (29%), Positives = 132/243 (54%), Gaps = 15/243 (6%) Query: 1 MSDLLEIRDVHKSFGAVKALDGVSMEINKGEVVALLGDNGAGKSTLIKIISGYHKPDRGD 60 ++ L + R VH S AV+A GE+V L G GAG+S L ++I G H+P G+ Sbjct: 262 VNHLTDNRKVHPSSLAVRA----------GEIVGLAGLVGAGRSELAQLIFGVHQPKGGE 311 Query: 61 LVFEGKKVIFNSPNDARSLGIETIYQ---DLALIPDLPIYYNIFLAREVTNKIF--LNKK 115 + +G+KV +SP DA + GI + + + L +L NI +A + + LN++ Sbjct: 312 IWIDGEKVKIHSPRDAIARGIGFLTENRKEQGLFLELAAQENIVMATIERDASYGLLNRR 371 Query: 116 KMMEESKKLLDSLQIRIPDINMKVENLSGGQRQAVAVARAVYFSAKMILMDEPTAALSVV 175 K + + + ++SL IR+P ++ LSGG +Q + ++R V + +++L+DEPT + V Sbjct: 372 KGQKIASEAIESLNIRVPHAQVRAGGLSGGNQQKLLISRWVSIAPRILLLDEPTRGVDVG 431 Query: 176 EARKVLELARNLKKKGLGVLIITHNIIQGYEVADRIYVLDRGKIIFHKKKEETNVEEITE 235 ++ + + ++G+ +L+I+ + + ++DR+YV+ G I +E + E I Sbjct: 432 AKSEIYRMMNQMAQQGVAILMISSELPEVVGMSDRVYVMREGSIAGELSGKEISQENIMT 491 Query: 236 VMT 238 + T Sbjct: 492 LAT 494 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: 229 Number of extensions: 9 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