Align Xanthosine permease; Xanthosine transporter (characterized)
to candidate BWI76_RS20600 BWI76_RS20600 nucleoside permease
Query= SwissProt::P45562 (418 letters) >FitnessBrowser__Koxy:BWI76_RS20600 Length = 418 Score = 724 bits (1870), Expect = 0.0 Identities = 354/418 (84%), Positives = 387/418 (92%) Query: 1 MSIAMRLKVMSFLQYFIWGSWLVTLGSYMINTLHFTGANVGMVYSSKGIAAIIMPGIMGI 60 M IA RLK+MSFLQYFIWGSWLVTLGSYMINTLHFTGANVGMVYSSKG+AAIIMPG+MGI Sbjct: 1 MGIASRLKLMSFLQYFIWGSWLVTLGSYMINTLHFTGANVGMVYSSKGLAAIIMPGVMGI 60 Query: 61 IADKWLRAERAYMLCHLVCAGVLFYAASVTDPDMMFWVMLVNAMAFMPTIALSNSVSYSC 120 IADKWLRAERAYMLCHLVCAGVL YA +VTDPD MFWVML+NAMA+MPTI+LSNSVSYSC Sbjct: 61 IADKWLRAERAYMLCHLVCAGVLLYATTVTDPDTMFWVMLINAMAYMPTISLSNSVSYSC 120 Query: 121 LAQAGLDPVTAFPPIRVFGTVGFIVAMWAVSLLHLELSSLQLYIASGASLLLSAYALTLP 180 LAQ+G DP TAFPP+RVFGT+GFIVAMW VSL+ LELSS QLYIAS ASLLL+ YA TLP Sbjct: 121 LAQSGQDPATAFPPVRVFGTLGFIVAMWMVSLMGLELSSAQLYIASAASLLLALYAFTLP 180 Query: 181 KIPVAEKKATTSLASKLGLDAFVLFKNPRMAIFFLFAMMLGAVLQITNVFGNPFLHDFAR 240 KIPV EKKA+T+LA++LGLDAFVLFKNPRMAIFF FAMMLGAVLQITNVFGNPFLHDFAR Sbjct: 181 KIPVTEKKASTTLAARLGLDAFVLFKNPRMAIFFFFAMMLGAVLQITNVFGNPFLHDFAR 240 Query: 241 NPEFADSFVVKYPSILLSVSQMAEVGFILTIPFFLKRFGIKTVMLMSMVAWTLRFGFFAY 300 NP FADSFVV+YPSILLSVSQMAEV FILTIPFFLKRFGIKTVMLMSM+AWTLRFGFFA+ Sbjct: 241 NPAFADSFVVRYPSILLSVSQMAEVAFILTIPFFLKRFGIKTVMLMSMLAWTLRFGFFAF 300 Query: 301 GDPSTTGFILLLLSMIVYGCAFDFFNISGSVFVEQEVDSSIRASAQGLFMTMVNGVGAWV 360 GDPS GF+LLL+SMIVYGCAFDFFNISGSVFVEQ+V ++IRASAQGLFMTMVNGVGAWV Sbjct: 301 GDPSPFGFVLLLMSMIVYGCAFDFFNISGSVFVEQQVGANIRASAQGLFMTMVNGVGAWV 360 Query: 361 GSILSGMAVDYFSVDGVKDWQTIWLVFAGYALFLAVIFFFGFKYNHDPEKIKHRAVTH 418 GS+LSG+AVDYFS+DGVKDWQTIWLVFA Y+L LAVIF F+Y H+PE+ + + H Sbjct: 361 GSVLSGLAVDYFSLDGVKDWQTIWLVFAAYSLMLAVIFALFFRYKHEPEQRMEKELAH 418 Lambda K H 0.330 0.141 0.435 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: 699 Number of extensions: 20 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: 418 Length of database: 418 Length adjustment: 32 Effective length of query: 386 Effective length of database: 386 Effective search space: 148996 Effective search space used: 148996 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 (21.9 bits) S2: 50 (23.9 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