Align gluconate:H+ symporter (gntT) (characterized)
to candidate PfGW456L13_5135 Gluconate transporter family protein
Query= reanno::Cup4G11:RR42_RS28835 (453 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_5135 Length = 449 Score = 591 bits (1524), Expect = e-173 Identities = 294/448 (65%), Positives = 364/448 (81%), Gaps = 4/448 (0%) Query: 6 GTTLLLYALIAVIALVVLIAKFKLNPFITLVVVSVLLGFAVGMPMGDIVKSFEAGVGGTL 65 G LL+YA IA+IAL+VLIA+++LNPFI + ++S+ L GMP +V ++EAGVG TL Sbjct: 6 GYWLLVYAAIAIIALIVLIARYRLNPFIVITLISIGLALVAGMPPSGVVGAYEAGVGKTL 65 Query: 66 GHIALVVGLGTMLGKMMAESGGAERIARTLIDAFGEKNVHWAMVTIAFIVGLPVFFEVGF 125 GHIALVV LGTMLGKMMAESGGAE++ARTLID FGEKN HWAMVTIAF+VGLP+FFEVGF Sbjct: 66 GHIALVVALGTMLGKMMAESGGAEQVARTLIDRFGEKNAHWAMVTIAFLVGLPLFFEVGF 125 Query: 126 VLLVPIAFNVAKRTGTSMVLVGIPMVAGLSVVHGLIPPHPAALLAVTAYKADIGKTILYA 185 VLLVPIAF VA+R G S+++VG+PMVAGLSVVH L+PPHPAA+LAV Y+A +G+T++YA Sbjct: 126 VLLVPIAFTVARRVGVSILMVGLPMVAGLSVVHALVPPHPAAMLAVQVYQASVGQTLMYA 185 Query: 186 LIVGIPTAAIAGPLFAKLMTRYVTLPDVNPLAAQFTEEDEGVKASHELPGFGITLFTILL 245 +++GIPTA IAGPL+AK + + LP NPL QF E + LPGFGIT+ TILL Sbjct: 186 ILIGIPTAIIAGPLYAKFIVPRIQLPAENPLERQFLERE----PRDSLPGFGITMATILL 241 Query: 246 PVILMLIGSWADLITTPKTFANDFLKLIGNSVIALLIAALVSFYTFGKRRGFTRENILRF 305 PV+LMLIG WA+LI+TP + N FL IGNSVIALL+A L+SF+T G +GF RE+IL+F Sbjct: 242 PVVLMLIGGWANLISTPGSGFNQFLLFIGNSVIALLLATLLSFWTLGLAQGFNRESILKF 301 Query: 306 TNECVAPTAIITLVVGAGGGFGRVLRDSGISNAIVDVATGAHVSVLLLGWLVAVLIRIAT 365 TNEC+APTA ITL+VGAGGG R+L D+G+++ IV +A H+S LL+GWL A L+RIAT Sbjct: 302 TNECLAPTASITLLVGAGGGLNRILVDAGVTDQIVGLAHEFHLSPLLMGWLFAALMRIAT 361 Query: 366 GSATVAMTTAAGIVAPIAASVPGTRPELLVLTTGAGSLILSHVNDGGFWLVKEYFNMTVA 425 GSATVAMTTA+G+VAP+A + PELLVL TGAGS+I SHVNDGGFWL+KEYFNMTV Sbjct: 362 GSATVAMTTASGVVAPVAIGLGYPHPELLVLATGAGSVIFSHVNDGGFWLIKEYFNMTVT 421 Query: 426 QTFKTWSVCETLISVIALLLTLALATVV 453 QTFKTW+V ETLISV+A LT+ L+ ++ Sbjct: 422 QTFKTWTVLETLISVVAFGLTVGLSYLI 449 Lambda K H 0.326 0.141 0.410 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: 805 Number of extensions: 52 Number of successful extensions: 3 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: 453 Length of database: 449 Length adjustment: 33 Effective length of query: 420 Effective length of database: 416 Effective search space: 174720 Effective search space used: 174720 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 (21.6 bits) S2: 51 (24.3 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