Align L-glutamine and L-histidine transporter (characterized)
to candidate N515DRAFT_0606 N515DRAFT_0606 basic amino acid/polyamine antiporter, APA family
Query= reanno::Korea:Ga0059261_1577 (470 letters) >FitnessBrowser__Dyella79:N515DRAFT_0606 Length = 477 Score = 315 bits (807), Expect = 2e-90 Identities = 180/438 (41%), Positives = 261/438 (59%), Gaps = 15/438 (3%) Query: 32 LVALGVGAIVGTGILTLIGVGAG-KAGPAVIMSFVIAGAICACAALAYAEMATMMPASGS 90 L A+G+G I+G G+ L G A AGPAV +SF+IAG A AAL YAE A ++P +GS Sbjct: 35 LTAIGIGGIIGVGVFVLAGQQAALNAGPAVAISFLIAGIASAAAALCYAEFAGLIPVTGS 94 Query: 91 AYAYSYAVLGEIIAWVVGWSLILEYSLVVSTVAVGWSGYAAPLLHAWTGMPLELMA---- 146 AY Y YAVLGE+ AW++GW L+LEY+L+V+ VA+GWSGY L A G+ L + A Sbjct: 95 AYTYGYAVLGELAAWLIGWDLLLEYALIVAVVAIGWSGYVQSAL-ASIGVDLPVWAKGAI 153 Query: 147 GPHANGIVNLPAIFIIAVVAGLLCLGTKESATLNAALVVVKIIALAVFVAVALPYFNGAN 206 G + N+ A + V+ LL T+ A N +V +K+ A+A+ + V Y N Sbjct: 154 GTGEGHVFNVVAALVTLGVSALLIFRTEWGARFNTFVVAIKVAAVALVIGVGAFYVKPEN 213 Query: 207 LEPFAPFGFAKTISPDGVE----RGVMAAAAIIFFAFYGFDAISTAAEETKNPGRDLAIG 262 PF P + + DGV +GV AAA++FFA +G+D ++TAAEE+KNP RDL Sbjct: 214 WVPFIP---ERIVGSDGVGHFGFQGVATAAAVVFFAVFGYDTLTTAAEESKNPQRDLPRA 270 Query: 263 IVGSMIACVAIYMLVAVAAVGATPFTHFANSPEPLALILRDLGRPGFATFLAVSAIIALP 322 ++ S+ +A+Y+ V++ G +T + P+A + LG A ++VSA+ L Sbjct: 271 VLLSLGISMAMYLAVSMVLTGIAHYTTL-KTDAPVADAFKGLGLHWVALTVSVSAVFGLI 329 Query: 323 TVLLGFLFGQSRIFFTMARDGMLPIGLAKVSKR-GSPVRITLFTAAIVAVIAGLLPIDEI 381 +VL F+ G +RI+F +ARDG+LP AK R G+P R T+ A++AGLLPI+E+ Sbjct: 330 SVLFAFMLGATRIWFALARDGLLPGWFAKPHPRYGTPHRPTIVLGVFTALVAGLLPIEEV 389 Query: 382 AALANAGTLAAFTAVAVCMMVLRVRAPDMPRMFRTPLWWLVGAIAVLGCIYLFFSLPVKT 441 A L N G L+AF + +++LR R PD+ R FRTPL L+ + + I+L LP T Sbjct: 390 AKLVNIGVLSAFIVICSSVLILRKRKPDLYRAFRTPLVPLIPLVGIGFSIWLLAELPWVT 449 Query: 442 QLWFLAWNALGVVIYFAY 459 FL W ++G+V+YF Y Sbjct: 450 WEVFLIWVSIGLVVYFGY 467 Lambda K H 0.327 0.140 0.426 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: 715 Number of extensions: 49 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: 470 Length of database: 477 Length adjustment: 33 Effective length of query: 437 Effective length of database: 444 Effective search space: 194028 Effective search space used: 194028 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: 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