Align Broadly selective nucleoside:Na+ cotransporter, hfCNT (transports uridine, thymidine, inosine, 3'-azido-3'deoxythymidine, 2'3'dideoxycytidine, and 2'3'dideoxyinosine) (Na+/uridine = 2) (characterized)
to candidate WP_055434951.1 ASC41_RS01910 Na+ dependent nucleoside transporter
Query= TCDB::Q9UA35 (683 letters) >NCBI__GCF_001418085.1:WP_055434951.1 Length = 577 Score = 264 bits (675), Expect = 8e-75 Identities = 167/471 (35%), Positives = 248/471 (52%), Gaps = 61/471 (12%) Query: 186 LDTAKRGANQVIP------------FFGLILYILLVFIFSKHPTKVRWRIVIWGLLLQFI 233 LDT K +IP G++ I + F+FS + + W+ V GL LQ I Sbjct: 117 LDTTKPEMGSIIPSQGFSLSSLWRGVLGMVTLIFVAFLFSSNRRGINWKTVGLGLALQLI 176 Query: 234 FGLIILRTKPGLDAFNWLGIQVQTFLKYTDAGSRFLFGDDFQ----DHFFAFAVLPIVIF 289 + +L+ F ++G L YT AGS FLFG FAF VLP +IF Sbjct: 177 IAIGVLKVSFVKTVFEFIGKGFIEILSYTQAGSEFLFGGMLDVTSFGFIFAFQVLPTIIF 236 Query: 290 FSTVMSMMYYLGLMQWLILKVGWLMQITMGTSPMESMVSAGNIFVGQTESPLLIRPYLAD 349 FS + S+++YLG++Q ++ +G L+ +G S ES+ AGNIF+GQTE+PLLI+ YL Sbjct: 237 FSALTSVLFYLGIIQKVVKLMGLLLTKVLGISGAESLSVAGNIFLGQTEAPLLIKAYLEK 296 Query: 350 LTISEMHSVMSSGFATIAGSVLGAYIS-LG--------IPAAHLLTASVMSAPAALAISK 400 + SE+ VM G AT+AG+VL AYI LG A HLL ASVM+AP A+ ISK Sbjct: 297 MNKSEILLVMIGGMATVAGAVLAAYIGFLGGEDEALQLFYAKHLLAASVMAAPGAIVISK 356 Query: 401 TFWPETKKSKNSTQTSIKLEKGQENNLVEAASQGASAAVPLVANIAANLIAFLAVLAFIN 460 +P+T++ + S ++ +N++EA + G + + L N+ A L+ F+A +A +N Sbjct: 357 ILFPQTEEVNTDVEVS---QEKIGSNILEAIANGTTEGLRLAVNVGAMLLVFVAFIAMVN 413 Query: 461 A----------------TLSWLGSMFN--------YPQFSFEIICSYVLMPFAFMMGVNY 496 L W + N Y S E + Y+ P +++GV Sbjct: 414 GIMGGIAGFNGLTIDALNLKWEFTSLNEVIEANTPYDSLSLEFLLGYIFAPLMWLIGVAR 473 Query: 497 DDSFLVAELLGMKTFFNEFVAYQRLSEYIHNRESGGPLFVDGVRQYMSVRSEAIATYALC 556 +D L+ +LLG+K +EF+ Y +L+E + V +S +ATY LC Sbjct: 474 EDMALMGQLLGIKLAASEFIGYIQLAELKN---------VANATHLTYEKSVIMATYMLC 524 Query: 557 GFANFGSLGIMIGGLSSLAPHRKSDIASCGIRALIAGTIACFSTACIAGVL 607 GFANF S+GI IGG+ SLAP ++ ++ G++ALI GTIA +A IAG++ Sbjct: 525 GFANFASIGIQIGGIGSLAPGQRKQLSKFGMKALIGGTIASLISATIAGMI 575 Lambda K H 0.325 0.139 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: 831 Number of extensions: 47 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: 683 Length of database: 577 Length adjustment: 38 Effective length of query: 645 Effective length of database: 539 Effective search space: 347655 Effective search space used: 347655 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 (21.6 bits) S2: 54 (25.4 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