Align histidine permease (characterized)
to candidate GFF4632 PS417_23700 aromatic amino acid transporter
Query= reanno::pseudo3_N2E3:AO353_12275 (468 letters) >lcl|FitnessBrowser__WCS417:GFF4632 PS417_23700 aromatic amino acid transporter Length = 467 Score = 381 bits (979), Expect = e-110 Identities = 193/453 (42%), Positives = 283/453 (62%), Gaps = 13/453 (2%) Query: 7 GLKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGPAVLLAYLIGGAAVFMVMRALGEM 66 GLKRGL RHI+ +ALG AIGTGLF GSA ++ AGP+++L Y I G F++MR LGEM Sbjct: 10 GLKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPSMILGYAIAGFIAFLIMRQLGEM 69 Query: 67 AVHNPVAGSFGQYASTYLGPMAGFILGWTYAFEMVIVGMADVTAFGIYMGFWFPEVSRWI 126 V PVAGSF +A Y G AGF+ GW Y V+VGMA++TA G Y+ FW+P++ W+ Sbjct: 70 IVEEPVAGSFSHFAHKYWGGYAGFLAGWNYWVLYVLVGMAELTAVGKYIQFWWPDIPTWV 129 Query: 127 WVLGVVSIVGGLNLCNVKVFGEMEFWLSLLKVAAIVAMILGGFGIMLFGISTAPGQVTDI 186 L V +N NVK FGE EFW +++KV AIV MI+ G ++ G G + Sbjct: 130 SALVFFVAVNLINTLNVKFFGETEFWFAIIKVVAIVGMIVLGCYLLFSGTG---GPQASV 186 Query: 187 SNLWTQGGFMPNGMGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQHVLPRAINAVPLRIL 246 SNLW+ GGF PNG GL+ S A +MF+FGG+E++G+TA EA +P+ V+P+AIN V RIL Sbjct: 187 SNLWSHGGFFPNGGMGLLMSMAFIMFSFGGLELVGITAAEASEPRKVIPKAINQVVYRIL 246 Query: 247 LFYVLTMLVLMSIFPWQQI---------GSQGSPFVQIFDKLGISSAATILNIVVITAAI 297 +FYV + VL+S++PW Q+ GSPFVQIF +G +AA ILN VV+TAA+ Sbjct: 247 IFYVGALTVLLSLYPWDQLLQTLGASGDAYSGSPFVQIFSLIGNDTAAHILNFVVLTAAL 306 Query: 298 SAINSDIFGAGRMMFGLAQQGHAPKGFAHLSRNGVPWMTVVVMSVALLLGVLLNYLIPEN 357 S NS ++ RM+FGLA+QG APK L++ GVP + + ++ +L V++NY+ P++ Sbjct: 307 SVYNSGVYCNSRMLFGLAEQGDAPKSLMKLNKQGVPIRALAISALVTMLCVVVNYVAPQS 366 Query: 358 VFLLIASIATFATVWVWLMILFTQVAMRRSMTAEQVAQLKFPVPFWPYAPMAAIAFMLFV 417 L+ ++ + + W +I T + R++M EQ F ++P++ +AFM+ + Sbjct: 367 ALELLFALVVASLMINWALISITHIKFRKAM-GEQGVTPSFKTFWFPFSNYLCLAFMVMI 425 Query: 418 FGVLGYFPDTQAALIVGVVWIVLLVLAYLMWVK 450 V+ P ++ VW+ ++ +AY + V+ Sbjct: 426 ISVMLAIPGISESVYAMPVWVGIIYVAYRLRVR 458 Lambda K H 0.329 0.142 0.441 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: 650 Number of extensions: 36 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: 468 Length of database: 467 Length adjustment: 33 Effective length of query: 435 Effective length of database: 434 Effective search space: 188790 Effective search space used: 188790 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 (21.8 bits) S2: 51 (24.3 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