Align Sodium/myo-inositol cotransporter 2; Na(+)/myo-inositol cotransporter 2; Sodium-dependent glucose cotransporter; Sodium/glucose cotransporter KST1; rKST1; Sodium/myo-inositol transporter 2; SMIT2; Solute carrier family 5 member 11 (characterized)
to candidate Echvi_1880 Echvi_1880 transporter, SSS family
Query= SwissProt::Q28728 (674 letters) >lcl|FitnessBrowser__Cola:Echvi_1880 Echvi_1880 transporter, SSS family Length = 624 Score = 284 bits (726), Expect = 1e-80 Identities = 165/487 (33%), Positives = 268/487 (55%), Gaps = 36/487 (7%) Query: 28 DIAVLVLYFLFVLAVGLW--STVKTKRDTVKGYFLAGGDMVWWPVGASLFASNVGSGHFV 85 D + ++Y L +++VGLW T K T + YFLA + WW VGASL A+N+ + HF+ Sbjct: 9 DYVIFIVYALAIVSVGLWVSRTKKGLEKTAQEYFLADKSLTWWAVGASLLAANISAEHFI 68 Query: 86 GLAGSGAATGISVAAYEFNGMFSVLMLAWIFLPIYIAGQVTTMPEYLRRRFGGSRIAITL 145 G +GSG A G+ ++AYE+ +++++A FLPI++ V TMP++L RF ++ Sbjct: 69 GTSGSGFAIGLGISAYEWIAAIALIIVAKYFLPIFLKHGVYTMPQFLSERF-NKGVSTAF 127 Query: 146 AVLYLFIYIFTKISVDMYAGAIFIQQSLHLDLYLSVVGLLAVTALYTVAGGLAAVIYTDA 205 AV +L +Y+F ++ Y GA+ + + + + L ++GLL + +Y++ GGL AV +TD Sbjct: 128 AVFWLLVYVFVNLTSVSYLGALALDKIMGIPLQYGIIGLLIFSGIYSIYGGLEAVAWTDV 187 Query: 206 LQTLIMLVGALTLMGYSFAAVGGMEGL-----------QEKYFLALPSNRSENSSCGLPR 254 +Q +I++ G L + AVG +G+ ++ + + +P R Sbjct: 188 VQVIILVAGGLITTFLALDAVGMGDGIFAGMSNLYNDAKDHFVMIMPQGRVMVPDGLGGS 247 Query: 255 EDAFHLFRDPLTSDLPWPG-ILFGMSIPSLWYWCTDQVIVQRSLAAKNLSHAKGGSLMAA 313 DAF DLP IL GM + +L YW +Q I+Q+ LAAK++ AK G L A Sbjct: 248 RDAF--------QDLPGLAVILGGMWLTNLGYWGFNQYIIQKGLAAKSIEEAKKGLLFAG 299 Query: 314 YLKVLPLFIMVFPGMVSRILFPDQVACADPETCQRVCNNP------SGCSDIAYPKLVLE 367 YLK+L I+V PG+ + +L D PE + N P SD AYP L+ Sbjct: 300 YLKLLMPIIVVIPGIAAYVLINDY----SPEQLAAILNMPVEHIGTIQKSDEAYPWLLRN 355 Query: 368 LLPTGLRGLMMAVMVAALMSSLTSIFNSASTIFTMDLWN-HVRPRASEKELMIVGRVFVL 426 +P G+RGL A + AA++SSL S+ NS STIFTMD++ + +P A+ +L+ GR+ + Sbjct: 356 FIPNGIRGLAFAALAAAIVSSLASMINSTSTIFTMDIYKVYFKPNANNHQLVRTGRIVAV 415 Query: 427 LLVLVSVLWIPVVQASQGGQLFVYIQAISSYLQPPVAMVFVLGCFWKRANEKGAFWGLVL 486 + + ++++ P Q + Q+F YIQ + Y+ P V +VF +G W++A A W + Sbjct: 416 VALAIAMIVAP--QLASLDQVFQYIQEYTGYIYPGVVVVFGMGLIWRQATASAALWTAIA 473 Query: 487 GLLLGFI 493 + G + Sbjct: 474 TIPAGIV 480 Lambda K H 0.325 0.138 0.426 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: 886 Number of extensions: 51 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 674 Length of database: 624 Length adjustment: 38 Effective length of query: 636 Effective length of database: 586 Effective search space: 372696 Effective search space used: 372696 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 54 (25.4 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 paper from 2022 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