Align Arbuscular mycorrhizal fungal proline:H+ symporter, AAP1 (binds and probably transports nonpolar, hydrophobic amino acids) (characterized)
to candidate WP_054653911.1 CES79_RS01340 amino acid permease
Query= TCDB::Q2VQZ4 (536 letters) >NCBI__GCF_002217945.1:WP_054653911.1 Length = 491 Score = 309 bits (792), Expect = 1e-88 Identities = 171/470 (36%), Positives = 259/470 (55%), Gaps = 23/470 (4%) Query: 30 NGG--LKQDLKNRHMQMIAIGGAIGAGLFVGSGGALQKGGPAALLIGYLIIGIMLLCTCL 87 NGG +K+ LK RH+ MIA+GG+IG GLFV SG A+ GP L+ Y+ +GIM+ Sbjct: 8 NGGNEVKRSLKTRHLSMIALGGSIGTGLFVASGSAISTAGPGGGLLAYVALGIMVYFLMT 67 Query: 88 ALAEMAVLYPVNGAFFTYIVRFVDPSWGFAMGWQYALAWLTVLPFELIAASITIRFWRED 147 +L EMA PV+G+F TY ++VDP+ GFAMGW Y W L ++ A++ ++FW + Sbjct: 68 SLGEMATNMPVSGSFATYSTKYVDPALGFAMGWNYWFNWAITLAVDISTAALVMKFWLPN 127 Query: 148 INMAVWVSVFLVVLMGIQIFGVRGYGEVEFVLSIIKICACVGFIILGIVINCGGVGDQ-- 205 + +W ++ LV++ I V+ +GE E+ +++IK+ V F+I+G G +G Sbjct: 128 VPGWIWSTIILVMIFMINALTVKAFGETEYWMAMIKVVTVVIFLIVGFATIFGIMGGHAT 187 Query: 206 GYIGVKYWRDPGAFTSFKGFCAVFVVAAFSFGGTEMVGLAAAESANPRKSIPMASKQVFW 265 G Y + P +VFVVA FSF GTE+VG+ A ESA P KS+P A QVFW Sbjct: 188 GLSNFTYKKAP-FVGGVPAILSVFVVAGFSFQGTELVGITAGESATPEKSVPKAINQVFW 246 Query: 266 RIAIFYILNLFIVGLILPANDPRLMGASGANTKASPFVLAIQDAGIKVLPSIMNAVITVA 325 RI +FYIL +F++ ++P P+L+G+S ++ SPF L + AG+ S+MNAVI + Sbjct: 247 RILLFYILAIFVIACLIPYTSPKLLGSSASDIAISPFTLVFERAGLAAAASVMNAVILTS 306 Query: 326 VLSVANSCTFGSTRTIQAMAERNMAPNFFKYIDSKGRPLYCVILQIAFGLLAYIGAAPQG 385 V+S ANS + S+R + ++A + AP +F++ G PL + G +A+I + G Sbjct: 307 VISAANSGMYASSRMLYSLALDDFAPKYFEHTTKNGVPLRAQVATTIVGAIAFI-TSIAG 365 Query: 386 MEIFGWLLALTGLGFLFVWGSICLAHIRMRAGMKAQGINLGLIPYKTPFGVAGSYLGLGL 445 E++ WL+A +GL W I ++H R R QG L + Y + G L L Sbjct: 366 PEVYSWLIAASGLTGFIAWVGIAISHFRFRRAFVKQGHQLSELKYHAKWFPFGPILAFVL 425 Query: 446 NILALIASFYTALFPASGASPTAEAFFS------SYLAFFSVTLLYLGYK 489 IL +I G +P+A F +YL+ +L+ YK Sbjct: 426 CILVII-----------GQNPSAFVHFDWKQIGVTYLSVPLFFILFFWYK 464 Lambda K H 0.327 0.142 0.442 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: 630 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: 536 Length of database: 491 Length adjustment: 35 Effective length of query: 501 Effective length of database: 456 Effective search space: 228456 Effective search space used: 228456 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: 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