Align Major myo-inositol transporter IolT (characterized)
to candidate WP_084931296.1 HA51_RS00995 sugar porter family MFS transporter
Query= SwissProt::O34718 (473 letters) >NCBI__GCF_002095475.1:WP_084931296.1 Length = 483 Score = 455 bits (1170), Expect = e-132 Identities = 238/453 (52%), Positives = 306/453 (67%), Gaps = 10/453 (2%) Query: 10 FLRTIILVSTFGGLLFGYDTGVLNGALPYMGEPDQLNLNAFTEGLVTSSLLFGAALGAVF 69 F++ I LV+T GGLLFGYDTGV++GAL +M D L L FT GLVTSSLLFGAA GA+ Sbjct: 24 FVKIIALVATLGGLLFGYDTGVVSGALLFMR--DDLQLTPFTTGLVTSSLLFGAAFGALL 81 Query: 70 GGRMSDFNGRRKNILFLAVIFFISTIGCTFAPNVTVMIISRFVLGIAVGGASVTVPAYLA 129 G +D GRRK I+ LA IF + +G FAP+V MI+SR LGIAVGGA+ TVP Y+A Sbjct: 82 AGHFADAMGRRKIIIMLAFIFALGAVGSAFAPDVVSMIVSRLFLGIAVGGAAATVPVYIA 141 Query: 130 EMSPVESRGRMVTQNELMIVSGQLLAFVFNAILGTTMGDNSHVWRFMLVIASLPALFLFF 189 E++P RG++VT ELMIVSGQLLA+V NA G H WR+ML I+++PA+ L+ Sbjct: 142 EIAPANKRGQLVTLQELMIVSGQLLAYVSNATFNEIWG-GEHTWRWMLAISTVPAVLLWL 200 Query: 190 GMIRMPESPRWLVSKGRKEDALRVLKKIRDEKRAAAELQEIEFAFKKEDQLEKATFKDLS 249 GMI MPESPRW V +G +A +VL+K R EL+EIE ++ Q K +DL Sbjct: 201 GMIFMPESPRWHVMRGNTGEARKVLEKTRAADDVEWELEEIEETIEENRQKGKGRLRDLK 260 Query: 250 VPWVRRIVFIGLGIAIVQQITGVNSIMYYGTEILRNSGFQTEAALIGNIANGVISVLATF 309 PW+R++ +G+GIA +QQ+TGVN+IMYY +L +G +AAL IANGVISVL T Sbjct: 261 TPWLRKVFLLGIGIAAIQQLTGVNTIMYYAPTMLTATGLSNDAALFATIANGVISVLMTL 320 Query: 310 VGIWLLGRVGRRPMLMTGLIGTTTALLLIGIFSLVL-------EGSPALPYVVLSLTVTF 362 VGIW++G++GRRP+++ G +G T L I + E + Y+VL+ + F Sbjct: 321 VGIWMIGKIGRRPLVLVGQMGCTACLFFIAAVCFFMPEYHVGGEVNLVRAYLVLTGMLMF 380 Query: 363 LAFQQGAISPVTWLMLSEIFPLRLRGLGMGVTVFCLWMVNFAVSFTFPILLAAIGLSTTF 422 L FQQGA+SPVTWL+LSEIFP RLRG+ MG VF LWM NFA+S FPILLAA GL+ F Sbjct: 381 LCFQQGALSPVTWLLLSEIFPARLRGICMGGAVFALWMANFAISMAFPILLAAFGLAGAF 440 Query: 423 FIFVGLGICSVLFVKRFLPETKGLSLEQLEENF 455 F +GI +FV R +PET+G SLEQ+E F Sbjct: 441 LAFAIIGIGGSMFVLRTIPETRGRSLEQIEHYF 473 Lambda K H 0.327 0.142 0.418 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: 667 Number of extensions: 25 Number of successful extensions: 4 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: 473 Length of database: 483 Length adjustment: 34 Effective length of query: 439 Effective length of database: 449 Effective search space: 197111 Effective search space used: 197111 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: 51 (24.3 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