Align Probable Glycine/alanine/asparagine/glutamine uptake porter, AgcS (characterized)
to candidate SM_b20069 SM_b20069 amino acid carrier protein
Query= TCDB::W0WFC6 (449 letters) >FitnessBrowser__Smeli:SM_b20069 Length = 467 Score = 614 bits (1583), Expect = e-180 Identities = 296/449 (65%), Positives = 367/449 (81%) Query: 1 MESLQKWVVDLNGVVWGPLMLVLILGTGLYLMLGLKFMPLVRLGVGFRLLWQGRSKDDES 60 ME+L ++ LNG+VWG M+VLI+GTGLYL L L FMP+ ++ GFR++ + R + Sbjct: 1 MEALNQFFNWLNGIVWGVPMIVLIIGTGLYLQLRLGFMPIRKVAYGFRMILKSRRPGRAA 60 Query: 61 SGEISPFQALMTCLAATVGTGNIAGVATAIFLGGPGALFWMWCTALVGMATKFSEVVLAV 120 GEI+P+ ALMT L+AT+GTGNIAGVATAI +GGPGALFWMW TA VGMATK++EVV+AV Sbjct: 61 EGEITPYAALMTALSATIGTGNIAGVATAIAVGGPGALFWMWVTAFVGMATKYAEVVVAV 120 Query: 121 HYREKDERNEHVGGPMYAIKNGLGKRWAWLGAAFALFGGLAGFGIGNMVQVNSMADALEV 180 YRE D++ EH GGPM+AIKNGLGK W WLG AFA+FGGLAGFGIGNMVQ N +A A+E Sbjct: 121 KYREVDDKGEHAGGPMFAIKNGLGKHWQWLGTAFAIFGGLAGFGIGNMVQANGIASAVEN 180 Query: 181 SFGVPDWVTGVATMLVTGLVILGGIRRIGKVAEALVPFMCVGYIVASVIVLVVHAEAIPG 240 +FG+ W++G+ ++TG VILGGI+RIG VAE +VPFM + Y+V VLVV A IP Sbjct: 181 AFGIETWISGIVMTVLTGAVILGGIKRIGAVAEKVVPFMAIFYLVCVAAVLVVFAGNIPQ 240 Query: 241 AFQLIFTHAFTPIAATGGFAGAAVMAAIRFGVARGIFSNEAGLGTAGIAQAAGTTHSAVR 300 A IFT AF+P AATGGF G+ V+ AIR GVARGIFSNEAGLGTAGIAQAAG+T + V Sbjct: 241 AIATIFTQAFSPTAATGGFLGSTVLMAIRMGVARGIFSNEAGLGTAGIAQAAGSTANPVF 300 Query: 301 SGLIGMLGTFIDTLIICSLTGLAIITSGVWTSGASGAALSSAAFEAAMPGVGHYILSLAL 360 SG+IGM+GTFIDT+I+C+LTGLAI+ SGVW SG +GA LSSAAFEAA+PG G+Y+++++L Sbjct: 301 SGVIGMMGTFIDTIIVCTLTGLAIMVSGVWASGETGAVLSSAAFEAALPGYGNYLVTISL 360 Query: 361 VVFAYTTILGWSYYGERCWEYLAGTRAILPFRIVWTLAIPFGAMTQLDFAWLVADTLNAL 420 +FA+TTILGW+YY E+CWEYL GT + +PFRIVWT+A+ FGA LDFAWLVADTLNAL Sbjct: 361 ALFAFTTILGWAYYAEKCWEYLIGTASAIPFRIVWTVAVFFGATLSLDFAWLVADTLNAL 420 Query: 421 MAIPNLIALLLLSPVVFRLTREYFAKARS 449 MAIPNLI+LLLLSPV+ +LTR+YFA+ R+ Sbjct: 421 MAIPNLISLLLLSPVIAQLTRDYFAEERA 449 Lambda K H 0.326 0.140 0.437 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: 737 Number of extensions: 43 Number of successful extensions: 1 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: 449 Length of database: 467 Length adjustment: 33 Effective length of query: 416 Effective length of database: 434 Effective search space: 180544 Effective search space used: 180544 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: 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