Align Alpha-ketoglutarate permease (characterized)
to candidate BPHYT_RS03430 BPHYT_RS03430 major facilitator transporter
Query= SwissProt::P0AEX3 (432 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS03430 BPHYT_RS03430 major facilitator transporter Length = 425 Score = 247 bits (631), Expect = 4e-70 Identities = 148/432 (34%), Positives = 230/432 (53%), Gaps = 13/432 (3%) Query: 6 VTADSKLTSSDTRRRIW-AIVGASSGNLVEWFDFYVYSFCSLYFAHIFFPSGNTTTQLLQ 64 + A + + + +R+ W A++ AS GN +EWFD VY F ++ A +FFP+GN T LL Sbjct: 1 MNATTAASLAGSRQNSWRAVIAASIGNALEWFDLVVYGFFAVIIAKLFFPAGNDTVSLLL 60 Query: 65 TAGVFAAGFLMRPIGGWLFGRIADKHGRKKSMLLSVCMMCFGSLVIACLPGYETIGTWAP 124 T G F F MRP+G + G AD+ GRK ++ LS+ +M G+L+IA LP Y++IG AP Sbjct: 61 TLGTFGVSFFMRPLGAIVIGAYADRAGRKAALTLSILLMMGGTLIIAILPTYQSIGLAAP 120 Query: 125 ALLLLARLFQGLSVGGEYGTSATYMSEVAVEGRKGFYASFQYVTLIGGQLLALLVVVVLQ 184 +L+LARL QG S GGE+G++ +++E V GR+GF+AS+Q + LLA V+L Sbjct: 121 VILVLARLMQGFSAGGEFGSATAFLAE-HVPGRRGFFASWQVASQGLTTLLAAGFGVLLT 179 Query: 185 HTMEDAALREWGWRIPFALGAVLAVVALWLRRQLDETSQQETRALKEAGSLKGLWRNRRA 244 + + WGWR+PF G ++ VA ++R +LDET + E + Sbjct: 180 GKLSPEQMASWGWRVPFFFGLLIGPVAWYIRTKLDETPEFLAAETTETPLRDTFTSQKLR 239 Query: 245 FIMVLGFTAAGSLCFYTFTTYMQKYLVNTAGMHANVASGIMTAALFVFMLIQPLIGALSD 304 ++ +G G++ Y +M + V G+ +VA + + M+ PL+G LSD Sbjct: 240 LLIAIGVVVLGTVSTY-LVLFMPTFGVKQLGLAPSVAFSAIALTGLIQMVFSPLVGHLSD 298 Query: 305 KIGRRTSMLCFGSLAAIFTVPILSALQNVSSPYAAFGL-----VMCALLIVSFYTSISGI 359 + GR T ML L + P L V+ P FG ++ L+ ++ ++ G+ Sbjct: 299 RHGRTTIMLSSALLLLVLIYPAFVYL--VAHP--TFGTLIAMQIVFGFLMTGYFAALPGL 354 Query: 360 LKAEMFPAQVRALGVGLSYAVANAIFGGSAEYVALSLKSIGMETAFFWYVTLMAVVAFLV 419 L +EMFP Q R G+ L+Y +A IFGG ++ L S+ A Y + A + LV Sbjct: 355 L-SEMFPVQTRTTGMSLAYNIAVTIFGGFGPFIIAWLISVTGSKAAPSYYLIFAAIVSLV 413 Query: 420 SLMLHRKGKGMR 431 +L R+ G R Sbjct: 414 ALTAARRKLGFR 425 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: 478 Number of extensions: 25 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: 432 Length of database: 425 Length adjustment: 32 Effective length of query: 400 Effective length of database: 393 Effective search space: 157200 Effective search space used: 157200 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