Align valine/tyrosine/tryptophan amino-acid permease (characterized)
to candidate WP_054653911.1 CES79_RS01340 amino acid permease
Query= CharProtDB::CH_091631 (619 letters) >NCBI__GCF_002217945.1:WP_054653911.1 Length = 491 Score = 283 bits (723), Expect = 2e-80 Identities = 164/485 (33%), Positives = 264/485 (54%), Gaps = 12/485 (2%) Query: 88 NNLTKSIKSRHLVMISLGTGIGTGLLVGNGQVLGTAGPAGLVLGYGIASIMLYCIIQAAG 147 N + +S+K+RHL MI+LG IGTGL V +G + TAGP G +L Y IM+Y ++ + G Sbjct: 11 NEVKRSLKTRHLSMIALGGSIGTGLFVASGSAISTAGPGGGLLAYVALGIMVYFLMTSLG 70 Query: 148 ELGLCYAGLTGNYTRYPSILVDPSLGFAVSVVYTIQWLTVLPLQLVTAAMTVKYWT-SVN 206 E+ ++G++ Y + VDP+LGFA+ Y W L + + TAA+ +K+W +V Sbjct: 71 EMATNMP-VSGSFATYSTKYVDPALGFAMGWNYWFNWAITLAVDISTAALVMKFWLPNVP 129 Query: 207 ADIFVAVVFVFVIIINLFGSRGYAEAEFIFNSCKILMVIGFVILAIIINCGGAGDRRYIG 266 I+ ++ V + +IN + + E E+ K++ V+ F+I+ G G Sbjct: 130 GWIWSTIILVMIFMINALTVKAFGETEYWMAMIKVVTVVIFLIVGFATIFGIMGGHATGL 189 Query: 267 AEYWHNPGPFAHGFKGVCTVFCYAAFSYGGIEVLLLSAAEQENPTKSIPNACKKVVYRIL 326 + + + PF G + +VF A FS+ G E++ ++A E P KS+P A +V +RIL Sbjct: 190 SNFTYKKAPFVGGVPAILSVFVVAGFSFQGTELVGITAGESATPEKSVPKAINQVFWRIL 249 Query: 327 LIYMLTTILVCFLVPYNSDELLGSSDSSGSHASPFVIAVASHGVKVVPHFINAVILISVI 386 L Y+L ++ L+PY S +LLGSS +S SPF + G+ +NAVIL SVI Sbjct: 250 LFYILAIFVIACLIPYTSPKLLGSS-ASDIAISPFTLVFERAGLAAAASVMNAVILTSVI 308 Query: 387 SVANSSLYSGPRLLLSLAEQGVLPKCLAYVDRNGRPLLCFFVSLVFGCIGFVATSDAEEQ 446 S ANS +Y+ R+L SLA PK + +NG PL + + G I F+ TS A + Sbjct: 309 SAANSGMYASSRMLYSLALDDFAPKYFEHTTKNGVPLRAQVATTIVGAIAFI-TSIAGPE 367 Query: 447 VFTWLLAISSLSQLFIWMSMSLSHIRFRDAMAKQGRSMNEVGYKAQTGYWGSWLAVLIAI 506 V++WL+A S L+ W+ +++SH RFR A KQG ++E+ Y A+ +G LA ++ I Sbjct: 368 VYSWLIAASGLTGFIAWVGIAISHFRFRRAFVKQGHQLSELKYHAKWFPFGPILAFVLCI 427 Query: 507 FFLVCQFWVAIAPVNEHGKLNVKVFFQNYLAMPIVLFAYFGHKIYFKSWSFWIPAEKIDL 566 ++ Q A + K YL++P+ +F +KI + + IP +K+D+ Sbjct: 428 LVIIGQNPSAFV------HFDWKQIGVTYLSVPLFFILFFWYKIKYHTGI--IPLDKVDV 479 Query: 567 DSHRN 571 H++ Sbjct: 480 TPHKH 484 Lambda K H 0.324 0.138 0.420 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: 712 Number of extensions: 36 Number of successful extensions: 8 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: 619 Length of database: 491 Length adjustment: 36 Effective length of query: 583 Effective length of database: 455 Effective search space: 265265 Effective search space used: 265265 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: 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