Align Alpha-ketoglutarate permease (characterized)
to candidate BWI76_RS21415 BWI76_RS21415 MFS transporter
Query= SwissProt::P0AEX3 (432 letters) >FitnessBrowser__Koxy:BWI76_RS21415 Length = 432 Score = 749 bits (1934), Expect = 0.0 Identities = 374/432 (86%), Positives = 397/432 (91%) Query: 1 MAESTVTADSKLTSSDTRRRIWAIVGASSGNLVEWFDFYVYSFCSLYFAHIFFPSGNTTT 60 M ES+++ DTRRRIWAIVGASSGNLVEWFDFYVYSFCSLYFAHIFFPSGNTTT Sbjct: 1 MTESSISERESQDHGDTRRRIWAIVGASSGNLVEWFDFYVYSFCSLYFAHIFFPSGNTTT 60 Query: 61 QLLQTAGVFAAGFLMRPIGGWLFGRIADKHGRKKSMLLSVCMMCFGSLVIACLPGYETIG 120 QLLQTAGVFAAGFLMRPIGGW+FGRIAD+ GRK SML+SVCMMCFGSLVIACLPGY TIG Sbjct: 61 QLLQTAGVFAAGFLMRPIGGWIFGRIADRRGRKTSMLISVCMMCFGSLVIACLPGYATIG 120 Query: 121 TWAPALLLLARLFQGLSVGGEYGTSATYMSEVAVEGRKGFYASFQYVTLIGGQLLALLVV 180 TWAPALLLLARLFQGLSVGGEYGTSATYMSEVAVEG+KGFYASFQYVTLIGGQLLA+LVV Sbjct: 121 TWAPALLLLARLFQGLSVGGEYGTSATYMSEVAVEGKKGFYASFQYVTLIGGQLLAVLVV 180 Query: 181 VVLQHTMEDAALREWGWRIPFALGAVLAVVALWLRRQLDETSQQETRALKEAGSLKGLWR 240 V LQ + D AL WGWRIPFALGAVLA+VALWLRRQLDETS+QETRALKEAGS KGLWR Sbjct: 181 VALQQILSDEALHAWGWRIPFALGAVLAIVALWLRRQLDETSKQETRALKEAGSFKGLWR 240 Query: 241 NRRAFIMVLGFTAAGSLCFYTFTTYMQKYLVNTAGMHANVASGIMTAALFVFMLIQPLIG 300 NR+AFIMVLGFTAAGSL FYTFTTYMQKYLVNTAGM A AS IMTAALFV+ML+QPL G Sbjct: 241 NRKAFIMVLGFTAAGSLSFYTFTTYMQKYLVNTAGMTAGTASMIMTAALFVYMLVQPLFG 300 Query: 301 ALSDKIGRRTSMLCFGSLAAIFTVPILSALQNVSSPYAAFGLVMCALLIVSFYTSISGIL 360 ALSDKIGRRTSMLCFG L +FTVPIL+ALQNVSSPYAAF LV+CALLIVSFYTSISGIL Sbjct: 301 ALSDKIGRRTSMLCFGVLVTVFTVPILNALQNVSSPYAAFALVICALLIVSFYTSISGIL 360 Query: 361 KAEMFPAQVRALGVGLSYAVANAIFGGSAEYVALSLKSIGMETAFFWYVTLMAVVAFLVS 420 KAEMFPAQVRALGVGLSYAVANA+FGGSAEYVALSLKS G+E AF+WYVT+M +AFLVS Sbjct: 361 KAEMFPAQVRALGVGLSYAVANALFGGSAEYVALSLKSAGIEHAFYWYVTVMGAIAFLVS 420 Query: 421 LMLHRKGKGMRL 432 L LHRKGKG+RL Sbjct: 421 LTLHRKGKGLRL 432 Lambda K H 0.328 0.138 0.419 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: 716 Number of extensions: 14 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: 432 Length of database: 432 Length adjustment: 32 Effective length of query: 400 Effective length of database: 400 Effective search space: 160000 Effective search space used: 160000 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 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