Align Monosaccharide-transporting ATPase, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate WP_043920019.1 jaqu_RS16085 sugar ABC transporter ATP-binding protein
Query= TCDB::G4FGN3 (494 letters) >NCBI__GCF_000877395.1:WP_043920019.1 Length = 498 Score = 340 bits (872), Expect = 7e-98 Identities = 181/484 (37%), Positives = 294/484 (60%), Gaps = 3/484 (0%) Query: 3 PILEVKSIHKRFPGVHALKGVSMEFYPGEVHAIVGENGAGKSTLMKIIAGVYQPDEGEII 62 P++ ++ + KR+ + AL V + GE + GENG+GKSTL+K++ GV +P G I+ Sbjct: 7 PLVTLEGVTKRYAAITALSEVDLTIRAGEAVCLAGENGSGKSTLIKVLVGVERPSAGRIL 66 Query: 63 YEGRGVRWNHPSEAINAGIVTVFQELSVMDNLSVAENIFMGDEEKRGIFIDYKKMYREAE 122 ++G P+ A AG+ +FQ+ S+ NLSVAENI M E G + +++ RE Sbjct: 67 FDGVPQTRLTPTAATRAGMQVIFQDFSLFPNLSVAENIAMTAERATGARLVHRRRARERA 126 Query: 123 KFMKEEFGIEIDPEEKLGKYSIAIQQMVEIARAVYKKAKVLILDEPTSSLTQKETEKLFE 182 + + + G+++D + ++ + +A +Q+V I RA+ A+++I+DEPT++LT++E +L + Sbjct: 127 REVLDRIGVDLDLDARVERLPVAHKQLVAICRALAADARLIIMDEPTTALTEREVARLLD 186 Query: 183 VVKSLKEKGVAIIFISHRLEEIFEICDKVSVLRDGEYIGTDSIENLTKEKIVEMMVGRKL 242 +++ LK GVA++F+SH+L E+ E+C+ V VLR+GE + E + M GR + Sbjct: 187 LIRRLKADGVAVLFVSHKLAEVLEVCEHVVVLRNGEKVADGPAETFDAASLTRAMTGRDV 246 Query: 243 EKFYIKEAHEPGEVVLEVKNLSGE-RFENVSFSLRRGEILGFAGLVGAGRTELMETIFGF 301 + + +L+V+NL+ + F +VS +LR GE+LG AGL+G+GRT L + +FG Sbjct: 247 AETPPEPLDPSASDLLKVENLTKDGAFRDVSLTLRAGEVLGVAGLLGSGRTSLAKALFGL 306 Query: 302 RPKRGGEIYIEGKRVEINHPLDAIEQGIGLVPEDRKKLGLILIMSIMHNVSLPSLDRIKK 361 G + ++G V + P+ A GIG VPEDR GL L SI N+++ L+ Sbjct: 307 ATPDSGRVTLDGTDVPLGDPIAAAGAGIGYVPEDRLTEGLFLEQSIARNIAVGRLEAHAS 366 Query: 362 GPFISFKRE-KELADWAIKTFDIRPAYPDRKVLYLSGGNQQKVVLAKWLALKPKILILDE 420 G ++ + +E A+W +K ++ P V LSGGNQQ+VVLA+W+A +P++LIL+ Sbjct: 367 GGVLNLRDLWEEAAEW-LKRLSVKAPDPQAPVRSLSGGNQQRVVLARWMARQPRVLILNG 425 Query: 421 PTRGIDVGAKAEIYRIMSQLAKEGVGVIMISSELPEVLQMSDRIAVMSFGKLAGIIDAKE 480 P+ G+DVG+KAEI+ I+S LA G+GVI+IS +LPE+L RI VM G + + E Sbjct: 426 PSVGVDVGSKAEIHAIISDLAARGLGVIVISDDLPELLGTCHRILVMKAGVITDEVAGGE 485 Query: 481 ASQE 484 E Sbjct: 486 GITE 489 Lambda K H 0.318 0.138 0.385 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: 579 Number of extensions: 27 Number of successful extensions: 6 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: 494 Length of database: 498 Length adjustment: 34 Effective length of query: 460 Effective length of database: 464 Effective search space: 213440 Effective search space used: 213440 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 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