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_037446034.1 N825_RS01525 sugar ABC transporter ATP-binding protein
Query= TCDB::G4FGN3 (494 letters) >NCBI__GCF_000576635.1:WP_037446034.1 Length = 496 Score = 403 bits (1035), Expect = e-117 Identities = 217/495 (43%), Positives = 318/495 (64%), Gaps = 7/495 (1%) Query: 4 ILEVKSIHKRFPGVHALKGVSMEFYPGEVHAIVGENGAGKSTLMKIIAGVYQPDEGEIIY 63 +L + + K FPGV AL V +E GEV A+VGENGAGKSTL+KI+ G+ +PD G I Sbjct: 1 MLALAGVSKSFPGVKALDDVRLELRAGEVMALVGENGAGKSTLVKILTGIERPDAGGITI 60 Query: 64 EGRGVRWNHPSEAINAGIVTVFQELSVMDNLSVAENIFMGDEEKRGI-----FIDYKKMY 118 +G V + P +A AGI + QE + D+L+VAENI MG G F+D++ M Sbjct: 61 DGSPVSFGSPHDAWLAGITAIHQETVMFDDLTVAENIHMGHHPTLGRGPFRRFVDWRAM- 119 Query: 119 REAEKFMKEEFGIEIDPEEKLGKYSIAIQQMVEIARAVYKKAKVLILDEPTSSLTQKETE 178 + + + ++I P+ L ++A + +V IA+A+ A+++I+DEPT++L+Q E Sbjct: 120 KARTRAVLARLEVDIQPDTVLRDLTVARKHIVGIAKALSHDARIVIMDEPTAALSQHEIA 179 Query: 179 KLFEVVKSLKEKGVAIIFISHRLEEIFEICDKVSVLRDGEYIGTDSIENLTKEKIVEMMV 238 +L+++V LK G AI+FISH+ +EIF I D+ +VLRDG +IG +I +T++++V MMV Sbjct: 180 ELYKIVGQLKAAGKAILFISHKFDEIFAIADRWTVLRDGRFIGAGAIGEVTRDELVTMMV 239 Query: 239 GRKLEKFYIKEAHEPGEVVLEVKNLSGE-RFENVSFSLRRGEILGFAGLVGAGRTELMET 297 GR+L++ + K GE VLEV +LS F+ + F LRRGEILGF GLVGAGR+E M+ Sbjct: 240 GRRLDQVFPKITVPLGETVLEVNDLSHPTEFDGIGFKLRRGEILGFYGLVGAGRSEAMQA 299 Query: 298 IFGFRPKRGGEIYIEGKRVEINHPLDAIEQGIGLVPEDRKKLGLILIMSIMHNVSLPSLD 357 +FG G + I G+ V + +P DAI GI VPEDR+ G IL M I N++LP +D Sbjct: 300 LFGITKPSRGRVRIAGRDVVVRNPSDAIRAGIAYVPEDRQVQGAILPMGITENITLPVVD 359 Query: 358 RIKKGPFISFKREKELADWAIKTFDIRPAYPDRKVLYLSGGNQQKVVLAKWLALKPKILI 417 R+ GP + RE+ +A + ++ + D+ V LSGGNQQKV++AKWLA P ++I Sbjct: 360 RVNGGPVLRPARERAVARRFGERLAVKATHWDQPVGTLSGGNQQKVLIAKWLATNPAVII 419 Query: 418 LDEPTRGIDVGAKAEIYRIMSQLAKEGVGVIMISSELPEVLQMSDRIAVMSFGKLAGIID 477 LDEPT+GIDVG+KA ++ M +L + G+ VI++SSELPE++ MSD I VM G++ Sbjct: 420 LDEPTKGIDVGSKAAVHEFMGELVRSGLAVILVSSELPEIMGMSDTIIVMHEGRIRRRFS 479 Query: 478 AKEASQEKVMKLAAG 492 EA+ E ++ A G Sbjct: 480 RAEATAEAIVTAATG 494 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: 631 Number of extensions: 31 Number of successful extensions: 7 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: 496 Length adjustment: 34 Effective length of query: 460 Effective length of database: 462 Effective search space: 212520 Effective search space used: 212520 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