Align Xanthosine permease; Xanthosine transporter (characterized)
to candidate WP_009124973.1 HMPREF9446_RS07490 nucleoside permease
Query= SwissProt::P45562 (418 letters) >NCBI__GCF_000195635.1:WP_009124973.1 Length = 414 Score = 465 bits (1197), Expect = e-135 Identities = 234/416 (56%), Positives = 295/416 (70%), Gaps = 8/416 (1%) Query: 1 MSIAMRLKVMSFLQYFIWGSWLVTLGSYMINTLHFTGANVGMVYSSKGIAAIIMPGIMGI 60 MSI RL M FLQ+F+WG+WL++LG YM TLHF G +G ++++ GIA+IIMPG+ GI Sbjct: 1 MSIKFRLTAMQFLQFFVWGAWLISLGGYMGGTLHFEGGQIGAIFATMGIASIIMPGLTGI 60 Query: 61 IADKWLRAERAYMLCHLVCAGVLFYAASVTDPDMMFWVMLVNAMAFMPTIALSNSVSYSC 120 IADKW+ AER Y + HL+ AG L YA++ T M+W ML+N +A+MPT+AL+N+VSY+ Sbjct: 61 IADKWVNAERLYGILHLIGAGALIYASTATTYSHMYWAMLLNMLAYMPTLALANTVSYNA 120 Query: 121 LAQAGLDPVTAFPPIRVFGTVGFIVAMWAVSLLHLELSSLQLYIASGASLLLSAYALTLP 180 L + +D + FPPIRV+GTVGFI AMWAV L + QLY+A+ ++ LL YA TLP Sbjct: 121 LEKYKMDLIKDFPPIRVWGTVGFICAMWAVDLTGFKTGVAQLYVAAASATLLGCYAFTLP 180 Query: 181 KIPVAEKKATTSLASKLGLDAFVLFKNPRMAIFFLFAMMLGAVLQITNVFGNPFLHDFAR 240 P + T L S GLDA +LFK +MAIFFLF+M+LGA LQITN +G+ FL FA Sbjct: 181 ACPPMRSEGKTML-SAFGLDALILFKQKKMAIFFLFSMLLGAALQITNTYGDLFLSSFAS 239 Query: 241 NPEFADSFVVKYPSILLSVSQMAEVGFILTIPFFLKRFGIKTVMLMSMVAWTLRFGFFAY 300 PE+ADSF VK+ ILLS+SQM+E FIL IPFFLK FGIK VML+SM AW RFG F Sbjct: 240 IPEYADSFGVKHSVILLSISQMSETLFILAIPFFLKHFGIKRVMLISMFAWVFRFGLFGL 299 Query: 301 GDPSTTGFILLLLSMIVYGCAFDFFNISGSVFVEQEVDSSIRASAQGLFMTMVNGVGAWV 360 GDP +G +L+LSMIVYG AFDFFN+SGS+F E E SIRASAQGLF M NG+GA + Sbjct: 300 GDPG-SGLWMLILSMIVYGMAFDFFNVSGSLFTEMEAHPSIRASAQGLFFMMTNGIGAII 358 Query: 361 GSILSGMAVDYFSV--DG----VKDWQTIWLVFAGYALFLAVIFFFGFKYNHDPEK 410 G SG VD FSV DG ++W +WL+FAGYAL + ++F F+Y H PEK Sbjct: 359 GGYASGAVVDAFSVYADGGGLISREWTPVWLIFAGYALVIGLLFGAVFRYKHTPEK 414 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: 574 Number of extensions: 28 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: 418 Length of database: 414 Length adjustment: 31 Effective length of query: 387 Effective length of database: 383 Effective search space: 148221 Effective search space used: 148221 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 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