Align Major myo-inositol transporter, IolT1, of 456 aas (characterized)
to candidate WP_058930749.1 AU252_RS11015 sugar porter family MFS transporter
Query= TCDB::E1WAV3 (456 letters) >NCBI__GCF_001484605.1:WP_058930749.1 Length = 479 Score = 272 bits (696), Expect = 2e-77 Identities = 143/461 (31%), Positives = 269/461 (58%), Gaps = 23/461 (4%) Query: 1 MGGILFGYDTAVISGAIGSLTSYFHLSPAETGWAVSCVVVGCVIGSFSAGYLSKRFGRKK 60 +GG LFG+D++V++GA+ ++ F LS A TG+AV+ ++GC G+F AG ++ R+GR Sbjct: 25 VGGFLFGFDSSVVNGAVDAIKDEFALSEAVTGFAVAIALLGCAAGAFLAGKVADRYGRIP 84 Query: 61 SLMVSALLFTISAVGTSLSYTFTHFVIYRIIGGLAVGLAATVSPMYMSEVSPKNMRGRAL 120 ++ + ALLF +SA+GT ++ + +R++GGL +GLA+ ++P Y+SE+SP+ +RGR Sbjct: 85 AMKLGALLFLVSAIGTGFAFGVWDLIFWRLVGGLGIGLASVIAPAYISEISPRQVRGRLA 144 Query: 121 SMQQFAIVFGQILIFYVNYKIASIAADT----WLIELGWRYMFAAGIIPCILFCILVFLI 176 S+QQ AI G + A+ A WL WR+MF A +P +++ + + + Sbjct: 145 SLQQLAITTGIFAALLSDALFATTAGGADQAFWLGLEAWRWMFLAAAVPAVVYGWIAYTL 204 Query: 177 PESPRWMMMIGREEETLKILTKISNEEHARHLLADIKTSLQNDQLNAHQ-KLNYRDGNVR 235 PESPR+++ G+E+E K+ I+ E + +I+ +++ D+L+ + L + ++ Sbjct: 205 PESPRFLVFQGKEDEARKVFDSIAPSEDTDRHIREIQDAIEEDKLSGQKGSLRGKTFGLQ 264 Query: 236 FILILGCMIAMLQQVTGVNVMMYYAPIVLKDVTGSAQEALFQTIWIGVIQLIGSIIGAMI 295 ++ +G ++++LQQ G+NV+ YY+ + K V +++L ++ + ++ +++ + Sbjct: 265 AVVWVGIVLSVLQQFVGINVIFYYSTTLWKAVGFQEKDSLTISVATSITNILVTLVAIAL 324 Query: 296 MDKMGRLSLMRKGTIGSIIGL----LLTSWALYS-------QATGYFALFGMLFFMIFYA 344 +D++GR ++ G+IG + L L S A+ S A G AL F++ + Sbjct: 325 VDRIGRRPILLAGSIGMAVSLGTMALAFSAAVGSGSEISLPGAWGPVALVAANIFVVSFG 384 Query: 345 LSWGVGAWVLISEIFPNRMRSQGMSISVGFMWMANFLVSQFFPMINENPYLLSHFHGAFP 404 SWG WVL+ EIFP+R+R++ + ++ W+ANF ++ FP++ L++ Sbjct: 385 ASWGPLVWVLLGEIFPSRIRARALGLAAAAQWVANFAITLSFPVMAAASLPLTYA----- 439 Query: 405 MWIFAICCIFSYFFICRYLPETKGISLEKMESVVLAKRRKK 445 ++A+ S+FF+ +PET G+SLE+ E++ + K KK Sbjct: 440 --MYALFAAASFFFVMFKVPETNGMSLEQAETLFVPKGSKK 478 Lambda K H 0.329 0.141 0.436 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: 603 Number of extensions: 28 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: 456 Length of database: 479 Length adjustment: 33 Effective length of query: 423 Effective length of database: 446 Effective search space: 188658 Effective search space used: 188658 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 (21.8 bits) S2: 51 (24.3 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