Align general amino acid permease AGP1 (characterized)
to candidate WP_054653911.1 CES79_RS01340 amino acid permease
Query= CharProtDB::CH_091105 (633 letters) >NCBI__GCF_002217945.1:WP_054653911.1 Length = 491 Score = 276 bits (707), Expect = 1e-78 Identities = 160/496 (32%), Positives = 261/496 (52%), Gaps = 22/496 (4%) Query: 109 TGHKSDSLKKTIQPRHVLMIALGTGIGTGLLVGNGTALVHAGPAGLLIGYAIMGSILYCI 168 +G+ + +K++++ RH+ MIALG IGTGL V +G+A+ AGP G L+ Y +G ++Y + Sbjct: 6 SGNGGNEVKRSLKTRHLSMIALGGSIGTGLFVASGSAISTAGPGGGLLAYVALGIMVYFL 65 Query: 169 IQACGEMALVYSNLTGGYNAYPSFLVDDGFGFAVAWVYCLQWLCVCPLELVTASMTIKYW 228 + + GEMA ++G + Y + VD GFA+ W Y W +++ TA++ +K+W Sbjct: 66 MTSLGEMA-TNMPVSGSFATYSTKYVDPALGFAMGWNYWFNWAITLAVDISTAALVMKFW 124 Query: 229 TTSVNPDVFVIIFYVLVITINIFGARGYAEAEFFFNCCKILMMTGFFILGIIIDVGGAGN 288 +V ++ I V++ IN + + E E++ K++ + F I+G A Sbjct: 125 LPNVPGWIWSTIILVMIFMINALTVKAFGETEYWMAMIKVVTVVIFLIVGF------ATI 178 Query: 289 DGFIGGKYWHDPGAFNGKHAIDRFKG----VAATLVTAAFAFGGSEFIAITTAEQSNPRK 344 G +GG H G N + F G + + V A F+F G+E + IT E + P K Sbjct: 179 FGIMGG---HATGLSNFTYKKAPFVGGVPAILSVFVVAGFSFQGTELVGITAGESATPEK 235 Query: 345 AIPGAAKQMIYRILFLFLATIILLGFLVPYNSDQLLGSTGGGTKASPYVIAVASHGVRVV 404 ++P A Q+ +RIL ++ I ++ L+PY S +LLGS+ SP+ + G+ Sbjct: 236 SVPKAINQVFWRILLFYILAIFVIACLIPYTSPKLLGSSASDIAISPFTLVFERAGLAAA 295 Query: 405 PHFINAVILLSVLSMANSSFYSSARLFLTLSEQGYAPKVFSYIDRAGRPLIAMGVSALFA 464 +NAVIL SV+S ANS Y+S+R+ +L+ +APK F + + G PL A + + Sbjct: 296 ASVMNAVILTSVISAANSGMYASSRMLYSLALDDFAPKYFEHTTKNGVPLRAQVATTIVG 355 Query: 465 VIAFCAASPKEEQVFTWLLAISGLSQLFTWTAICLSHLRFRRAMKVQGRSLGELGFKSQT 524 IAF + E V++WL+A SGL+ W I +SH RFRRA QG L EL + ++ Sbjct: 356 AIAFITSIAGPE-VYSWLIAASGLTGFIAWVGIAISHFRFRRAFVKQGHQLSELKYHAKW 414 Query: 525 GVWGSAYACIMMILILIAQFWVAIAPIGEGKLDAQAFFENYLAMPILIALYVGYKVWHKD 584 +G A ++ IL++I Q P D + YL++P+ L+ YK+ K Sbjct: 415 FPFGPILAFVLCILVIIGQ-----NPSAFVHFDWKQIGVTYLSVPLFFILFFWYKI--KY 467 Query: 585 WKLFIRADKIDLDSHR 600 I DK+D+ H+ Sbjct: 468 HTGIIPLDKVDVTPHK 483 Lambda K H 0.324 0.138 0.424 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: 778 Number of extensions: 42 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: 633 Length of database: 491 Length adjustment: 36 Effective length of query: 597 Effective length of database: 455 Effective search space: 271635 Effective search space used: 271635 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: 41 (22.0 bits) S2: 53 (25.0 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