Align general amino acid permease AGP1 (characterized)
to candidate GFF4632 PS417_23700 aromatic amino acid transporter
Query= CharProtDB::CH_091105 (633 letters) >lcl|FitnessBrowser__WCS417:GFF4632 PS417_23700 aromatic amino acid transporter Length = 467 Score = 219 bits (559), Expect = 2e-61 Identities = 145/470 (30%), Positives = 235/470 (50%), Gaps = 30/470 (6%) Query: 116 LKKTIQPRHVLMIALGTGIGTGLLVGNGTALVHAGPAGLLIGYAIMGSILYCIIQACGEM 175 LK+ ++ RH+ +IALG IGTGL +G+ L AGP+ +++GYAI G I + I++ GEM Sbjct: 11 LKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPS-MILGYAIAGFIAFLIMRQLGEM 69 Query: 176 ALVYSNLTGGYNAYPSFLVDDGFGFAVAWVYCLQWLCVCPLELVTASMTIKYWTTSVNPD 235 +V + G ++ + GF W Y + ++ V EL I++W + Sbjct: 70 -IVEEPVAGSFSHFAHKYWGGYAGFLAGWNYWVLYVLVGMAELTAVGKYIQFWWPDIPTW 128 Query: 236 VFVIIFYVLVITINIFGARGYAEAEFFFNCCKILMMTGFFILGIIIDVGGAGNDGFIGGK 295 V ++F+V V IN + + E EF+F K++ + G +LG + G G Sbjct: 129 VSALVFFVAVNLINTLNVKFFGETEFWFAIIKVVAIVGMIVLGCYLLFSGTGGPQASVSN 188 Query: 296 YWHDPGAF-NGKHAIDRFKGVAATLVTAAFAFGGSEFIAITTAEQSNPRKAIPGAAKQMI 354 W G F NG G+ ++ F+FGG E + IT AE S PRK IP A Q++ Sbjct: 189 LWSHGGFFPNGG------MGLLMSMAFIMFSFGGLELVGITAAEASEPRKVIPKAINQVV 242 Query: 355 YRILFLFLATIILLGFLVPYNSD-QLLGSTGGGTKASPYVIAVASHGVRVVPHFINAVIL 413 YRIL ++ + +L L P++ Q LG++G SP+V + G H +N V+L Sbjct: 243 YRILIFYVGALTVLLSLYPWDQLLQTLGASGDAYSGSPFVQIFSLIGNDTAAHILNFVVL 302 Query: 414 LSVLSMANSSFYSSARLFLTLSEQGYAPKVFSYIDRAGRPLIAMGVSALFAVIAFCAASP 473 + LS+ NS Y ++R+ L+EQG APK +++ G P+ A+ +SAL ++ Sbjct: 303 TAALSVYNSGVYCNSRMLFGLAEQGDAPKSLMKLNKQGVPIRALAISALVTMLCVVVNYV 362 Query: 474 KEEQVFTWLLAISGLSQLFTWTAICLSHLRFRRAMKVQGRSLGELGFKSQTGVW--GSAY 531 + L A+ S + W I ++H++FR+AM QG + FK+ W S Y Sbjct: 363 APQSALELLFALVVASLMINWALISITHIKFRKAMGEQGVT---PSFKT---FWFPFSNY 416 Query: 532 ACIMMILILIAQFWVAIAPIGEGKLDAQAFFENYLAMPILIA-LYVGYKV 580 C + +++I +AI I E+ AMP+ + +YV Y++ Sbjct: 417 LC-LAFMVMIISVMLAIPGIS----------ESVYAMPVWVGIIYVAYRL 455 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: 692 Number of extensions: 35 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: 467 Length adjustment: 35 Effective length of query: 598 Effective length of database: 432 Effective search space: 258336 Effective search space used: 258336 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: 52 (24.6 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