Align General amino-acid permease GAP2 (characterized)
to candidate WP_051056359.1 LACPOB_RS0100170 amino acid permease
Query= SwissProt::A0A1D8PK89 (588 letters) >NCBI__GCF_000349725.1:WP_051056359.1 Length = 470 Score = 341 bits (875), Expect = 3e-98 Identities = 184/469 (39%), Positives = 274/469 (58%), Gaps = 16/469 (3%) Query: 88 MIAIGGSIGTGLFVGSGSSLHTGGPAGLLIAYILIGTMIYCTVMSLGELAVTFPVSGAFV 147 MIA+GGSIGTGLFV SGS++ T GP G L+AYI IG M+Y + SLGE+A PV+G+F Sbjct: 1 MIALGGSIGTGLFVASGSAISTAGPGGALVAYIGIGLMVYFLMTSLGEMATYLPVTGSFA 60 Query: 148 TYNSRFIDPSWGFAMAWNYAMQWLVVLPLELVAAAMTVKYWDAKTNSAAFVVIFYVLIVA 207 TY RF+DP+ GFAM WNY W + L +++ + +K+W + S AF V +I Sbjct: 61 TYARRFVDPAMGFAMGWNYWFNWAITLAVDVSTVGLVLKFWFPRVPSWAFSVGALAIIFI 120 Query: 208 INFFGVRGYGEAEFIFSAVKVLAVLGFIILGIVLCAGGGPQGGYIGGKNWYIEG-----A 262 IN V +GE E+ + +KV+ V+ F+++G + G I G Y+E A Sbjct: 121 INALSVNSFGETEYWMALIKVVTVIVFLVVGFLTIFG------IINGHATYLENFVYRKA 174 Query: 263 PFPNGAKGVITVFVNAAFAFAGTELCGLAAAETENPRKSLPKACKQVFWRITLFYVICLT 322 PF G +++VFV A F+F GTEL G+ A E+ENP +S+PKA KQVFWRI LFY++ + Sbjct: 175 PFVGGIPTILSVFVVAGFSFQGTELIGITAGESENPGESIPKAIKQVFWRIILFYILSIF 234 Query: 323 LVGLLVPWNDERLLGSSSADASASPFVISIRNAGIKGLPSVMNVVIMIAVLSVGNSSVYG 382 ++ L+P+ LLGS + D + SPF + R AG+ G +MN VI+ +VLS NS +Y Sbjct: 235 VIAALIPYTSPNLLGSDAGDVTISPFTLVFRRAGLAGAAGIMNAVILTSVLSAANSGMYA 294 Query: 383 SSRTLAALAASNQAPKIFGYIDKQGRPLVGIIAQLLVGLLCFLAASDKQGEVFNWLLALS 442 S+R L +L S APKIF ++ +G P+ ++ VGL+ F A S ++N+L++ S Sbjct: 295 STRMLFSLGVSGDAPKIFKRVNTRGIPMPALVGTAAVGLITF-ATSIFGDRIYNFLVSAS 353 Query: 443 GLSSIFTWGSINVCLIRFRRALAAQGRDTGELVFTSQVGVIGAIWGAFLNTVVLCLQFWI 502 GLS W I + RFRRA AQG D EL + ++ G I L +V+ Q Sbjct: 354 GLSGFIAWVGIAISHYRFRRAFKAQGHDLSELQYHAKWFPFGPILALILCILVIIGQDLG 413 Query: 503 AVWPLHSSPSAEAFFSAYLTVPVVIVFYVGHKLWTKNWQVYICAKDIDI 551 + +S +A +Y++VP+ ++ ++ +K+ K + + D+ I Sbjct: 414 S----FASFDWQAILFSYMSVPLFLILFIYYKIRHKTKLIPLEEVDLTI 458 Lambda K H 0.324 0.139 0.431 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: 765 Number of extensions: 33 Number of successful extensions: 4 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: 588 Length of database: 470 Length adjustment: 35 Effective length of query: 553 Effective length of database: 435 Effective search space: 240555 Effective search space used: 240555 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.5 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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:
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