Align Facilitated trehalose transporter Tret1; AmTRET1 (characterized)
to candidate 16922 b2841 arabinose transporter (NCBI)
Query= SwissProt::A9ZSY2 (502 letters) >lcl|FitnessBrowser__Keio:16922 b2841 arabinose transporter (NCBI) Length = 472 Score = 215 bits (547), Expect = 3e-60 Identities = 135/451 (29%), Positives = 237/451 (52%), Gaps = 21/451 (4%) Query: 41 MQLLAALAVSMASLMIGYSSSYTSPALVSMRDNTTATFEVTMDMAMWIGSIMPLSALIGG 100 M + ++A ++A L+ G + AL + D+ F +T + W+ S M L A IG Sbjct: 21 MNMFVSVAAAVAGLLFGLDIGVIAGALPFITDH----FVLTSRLQEWVVSSMMLGAAIGA 76 Query: 101 IIGGPCIEYIGRRNTILSTALPFLAGWLFIALATNVAMILVGRSICGFCVGVASLSLPVY 160 + G +GR+ ++++ A+ F+ G + A AT+V M++ R + G VG+AS + P+Y Sbjct: 77 LFNGWLSFRLGRKYSLMAGAILFVLGSIGSAFATSVEMLIAARVVLGIAVGIASYTAPLY 136 Query: 161 LGESIQPEVRGSLGLLPTVFGNSGILMCF---TAGMYLA-WRNLALLGACIPIIFLILMF 216 L E VRG + + + GI++ F TA Y WR + + A ++ +IL+ Sbjct: 137 LSEMASENVRGKMISMYQLMVTLGIVLAFLSDTAFSYSGNWRAMLGVLALPAVLLIILVV 196 Query: 217 LIPETPRWYISKGKIKEARKSLQWLRGKTADISEELDSIQKMHIESERIATEGALIELFR 276 +P +PRW KG+ EA + L+ LR + EEL+ I+ ES ++ G + Sbjct: 197 FLPNSPRWLAEKGRHIEAEEVLRMLRDTSEKAREELNEIR----ESLKLKQGGWALFKIN 252 Query: 277 KNHIKPVFISLGLMFFQQFSGINAVIFYTVQIFKDSGSTVDEN--LSTIIVGLVNFISTF 334 +N + VF+ + L QQF+G+N +++Y +IFK +G T E ++T++VGL +TF Sbjct: 253 RNVRRAVFLGMLLQAMQQFTGMNIIMYYAPRIFKMAGFTTTEQQMIATLVVGLTFMFATF 312 Query: 335 VAAMIIDRLGRKMLLYISSILMCITLFTFGTFFYVKELMDVTA---FGWIPLMSLIVYVI 391 +A +D+ GRK L I +M + G + + + + TA W+ + ++ + Sbjct: 313 IAVFTVDKAGRKPALKIGFSVMALGTLVLG--YCLMQFDNGTASSGLSWLSVGMTMMCIA 370 Query: 392 GFSFGFGPIPWLMMGEILPVKIRGTAASVATAFNWSCTFVVTKTYEDLVLHIGPYGTFWL 451 G++ P+ W++ EI P+K R + +T NW ++ T+ L+ IG GTFWL Sbjct: 371 GYAMSAAPVVWILCSEIQPLKCRDFGITCSTTTNWVSNMIIGATFLTLLDSIGAAGTFWL 430 Query: 452 FGTLVAVAFIFVII-CVPETRGRSLEEIERR 481 + T + +AF+ + +PET+ +LE IER+ Sbjct: 431 Y-TALNIAFVGITFWLIPETKNVTLEHIERK 460 Lambda K H 0.327 0.141 0.425 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: 608 Number of extensions: 31 Number of successful extensions: 6 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: 502 Length of database: 472 Length adjustment: 34 Effective length of query: 468 Effective length of database: 438 Effective search space: 204984 Effective search space used: 204984 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: 52 (24.6 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