Align The Na+-dependent sugar transporter, HP1174 (transports glucose, galactose, mannose and 2-deoxyglucose (Psakis et al. 2009)). (most similar to 2.A.1.7.2; 49% identity) (characterized)
to candidate 7025962 Shewana3_3110 glucose/galactose transporter (RefSeq)
Query= TCDB::O25788 (407 letters) >lcl|FitnessBrowser__ANA3:7025962 Shewana3_3110 glucose/galactose transporter (RefSeq) Length = 432 Score = 180 bits (456), Expect = 8e-50 Identities = 146/432 (33%), Positives = 215/432 (49%), Gaps = 41/432 (9%) Query: 2 QKTSNTLALGSLTALFFLMGFITVLNDILIPHLKPIFDLTYFEASLIQFCFFGAYFIMGG 61 Q+ S+ L + + ALFF++GF T LN L+P+LK I L F+ASLI F F+ A Sbjct: 7 QQKSSFLPMAIVAALFFILGFATWLNGSLMPYLKQILQLNPFQASLILFSFYIAVTFTAL 66 Query: 62 VFGNVISKIGYPFGVVLGFVITATGCALFYPAAHFGSYGFFLGALFILASGIVCLQTAGN 121 VI K+GY G+ LG I LF PAA +G FL A ++ +G LQTA N Sbjct: 67 PSAWVIRKVGYKNGMALGMGIMMLAGLLFIPAAKTQIFGLFLCAQLVMGTGQTLLQTAVN 126 Query: 122 PFVTLLSKGKEARNLVLVQAFNSLGT-TLGPIFGSLLIFSTTKMGDNASLIDKLAD--AK 178 P+V L + A V V + G + P+ S LI + K +L D A Sbjct: 127 PYVVRLGPEESAAARVSVMGILNKGAGVIAPLVFSALILDSFKDRIGTTLTQVQIDEMAN 186 Query: 179 SVQMPYLGLAVFSLLLALIMYLLKLPDV--EKEMPKETTQ---KSLFSHKHFVFGALGIF 233 S+ PYLG+A+F +LAL + LP++ E E+ + T + K+ SH + FG + +F Sbjct: 187 SLVFPYLGMAIFIGVLALAVKKSPLPELSNEDEVAEHTDKGQIKAALSHPNLAFGVIALF 246 Query: 234 FYVGGEVAIGSFLVLSFEKLLNLDSQSSAHYLV---YYWGGAMVGRFLGSVLMNK-IAPN 289 YV EV G + +F L ++ HY V Y ++G LG +L+ + I+ Sbjct: 247 VYVAVEVIAGD-TIGTFALSLGVE-----HYGVMTSYTMVCMVLGYTLGIILIPRFISQP 300 Query: 290 KYLAFNALSSIVLIALAIIIG---------------GKIA----LFALTFVGFFNSIMFP 330 L +A+ + L+ LAI+ G G +A L + F+G N+I++P Sbjct: 301 TALMISAILGL-LLTLAILFGDNNSYAIANALLVPFGGVALPDTLLFIAFLGLANAIVWP 359 Query: 331 TIFSLATLNLGHLTSKASGVISMAIVGGALIPPIQGAVTDMLTATESNLLYAYGVPLLCY 390 ++ LA LG LTS S ++ M I GGA P G + +AT+ Y V L CY Sbjct: 360 AVWPLALSGLGKLTSTGSALLIMGIAGGAFGPLFWGLTS---SATDMGQQGGYMVMLPCY 416 Query: 391 FYILFFALKGYK 402 +ILF+A+KG+K Sbjct: 417 LFILFYAVKGHK 428 Lambda K H 0.328 0.144 0.423 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: 466 Number of extensions: 22 Number of successful extensions: 5 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: 407 Length of database: 432 Length adjustment: 32 Effective length of query: 375 Effective length of database: 400 Effective search space: 150000 Effective search space used: 150000 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
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