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 GFF2673 PS417_13635 D-ribose transporter ATP-binding protein
Query= TCDB::G4FGN3 (494 letters) >FitnessBrowser__WCS417:GFF2673 Length = 510 Score = 419 bits (1077), Expect = e-121 Identities = 232/501 (46%), Positives = 335/501 (66%), Gaps = 10/501 (1%) Query: 1 MKPILEVKSIHKRFPGVHALKGVSMEFYPGEVHAIVGENGAGKSTLMKIIAGVYQPDEG- 59 ++P+LE++ I K F G+ LK V ++ YPGE+HA++GENGAGKSTLMKI++G YQ D G Sbjct: 3 LEPLLEMQGISKTFNGLRVLKTVGLKVYPGEIHALMGENGAGKSTLMKILSGAYQADPGG 62 Query: 60 EIIYEGRGVRWNHPSEAINAGIVTVFQELSVMDNLSVAENIFMGDEEKRGIFIDYKKMYR 119 EI G+ + P+ A GI ++QELS+ NLSVAENI++G E +RG ID K M Sbjct: 63 EIRIAGQLIPTFDPATAKALGIAVIYQELSLCPNLSVAENIYLGRELRRGWTIDRKGMEA 122 Query: 120 EAEKFMKEEFGIEIDPEEKLGKYSIAIQQMVEIARAVYKKAKVLILDEPTSSLTQKETEK 179 + + + G E P ++ SIA +Q+VEIARA++ AK+L++DEPT+ L+ +ET++ Sbjct: 123 GCIEVL-QRLGAEFTPATRVSSLSIAERQLVEIARALHAHAKILVMDEPTTPLSSRETDR 181 Query: 180 LFEVVKSLKEKGVAIIFISHRLEEIFEICDKVSVLRDGEYIGTDSIENLTKEKIVEMMVG 239 LF ++K L+ +G+AII+ISHR+ EI+ + D+VSVLRDG YIG + + L+ E +V+MMVG Sbjct: 182 LFALIKQLRSQGLAIIYISHRMAEIYALSDRVSVLRDGHYIGELTRDALSAEALVKMMVG 241 Query: 240 RKLEKFYIKE--AHEPGEVVLEVKNLS-GERFENVSFSLRRGEILGFAGLVGAGRTELME 296 R L FY KE A+ PG VV+ V++++ G+R + SF L GE+LG AGLVGAGRTEL Sbjct: 242 RDLSGFYKKEHAAYNPGNVVMRVRDMADGKRVRHCSFDLHAGEVLGIAGLVGAGRTELAR 301 Query: 297 TIFGFRPKRGGEIYIEGKRV-EINHPLDAIEQGIGLVPEDRKKLGLILIMSIMHNVSL-P 354 IF P+ G + + GK V + P DAI G+ + EDRK GL L MS+ N+++ Sbjct: 302 LIFAADPRTSGTLEVVGKAVTPLRTPADAIRAGVVYLTEDRKAQGLFLDMSVADNINVCA 361 Query: 355 SLDRIKKGPFISFKREKELADWAIKTFDIRPAYPDRKVLYLSGGNQQKVVLAKWLALKPK 414 + G + + ++ AIK+ IR A LSGGNQQKV+LA+ L +KP Sbjct: 362 CVPDAHAGGVLDRDHALQRSNDAIKSLSIRVASGKVNAGALSGGNQQKVLLARLLEVKPH 421 Query: 415 ILILDEPTRGIDVGAKAEIYRIMSQLAKEGVGVIMISSELPEVLQMSDRIAVMSFGKL-- 472 +LILDEPTRG+D+G+K+EIYRI++QLA+ G+G+++ISSELPE++ DR+ +M G+L Sbjct: 422 VLILDEPTRGVDIGSKSEIYRIINQLAQAGIGIVVISSELPEIIGTCDRVLIMREGQLVA 481 Query: 473 -AGIIDAKEASQEKVMKLAAG 492 G + SQE+++ LA G Sbjct: 482 EVGGASGQAISQERIIDLATG 502 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: 679 Number of extensions: 37 Number of successful extensions: 10 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: 510 Length adjustment: 34 Effective length of query: 460 Effective length of database: 476 Effective search space: 218960 Effective search space used: 218960 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