Align Glucose facilitated diffusion protein (characterized)
to candidate WP_010538095.1 KCY_RS0116360 D-xylose transporter XylE
Query= SwissProt::P21906 (473 letters) >NCBI__GCF_000226135.1:WP_010538095.1 Length = 484 Score = 315 bits (808), Expect = 2e-90 Identities = 180/494 (36%), Positives = 277/494 (56%), Gaps = 36/494 (7%) Query: 2 SSESSQGLVTRLALIAAIGGLLFGYDSAVIAAIGTPVDIHFIAPRHLSATAAASLSGMVV 61 ++E S+ + + +A +GGLLFGYD+AVI+ ++ F++ + G+ Sbjct: 5 TNEGSKLYLYSITSVAILGGLLFGYDTAVISGAEKGLEAFFLSASDFQYNKV--MHGITS 62 Query: 62 VAVLVGCVTGSLLSGWIGIRFGRRGGLLMSSICFVAAGFGAALTEKLFGTGGSA----LQ 117 + L+GCV G LSG R GRR L ++++ F + G+ E LF G L Sbjct: 63 SSALIGCVLGGALSGIFASRLGRRNSLRLAAVLFFLSALGSYYPEVLFFEYGKPNMDLLI 122 Query: 118 IFCFFRFLAGLGIGVVSTLTPTYIAEIAPPDKRGQMVSGQQMAIVTGALTGYIFTWLLA- 176 F +R L G+G+G+ S + P YIAEIAP + RG +VS Q AI+ G L Y +L+ Sbjct: 123 AFNLYRVLGGIGVGLASAVCPMYIAEIAPSNIRGTLVSCNQFAIIFGMLVVYFVNYLIMG 182 Query: 177 -HFGSID----------------WVNASGWCWSPASEGLIGIAFLLLLLTAPDTPHWLVM 219 H I W GW + SE F +LL P TP +LV+ Sbjct: 183 DHQNPIILKDAAGVLSVSTESDMWTVQEGWRYMFGSEAFPAALFGMLLFFVPKTPRYLVL 242 Query: 220 KGRHSEASKILARLEPQADPNLTIQKIKAGFDKAMDKSSAGLFAFGITVVFAGVSVAAFQ 279 + +A IL ++ +A + IKA + +K +F +G+TV+ G+ ++ FQ Sbjct: 243 VQQEEKAYSILEKINGKAKAREILNDIKATAQEKTEK----IFTYGVTVIVIGILLSVFQ 298 Query: 280 QLVGINAVLYYAPQMFQNLGFGADTALLQTISIGVVNFIFTMIASRVVDRFGRKPLLIWG 339 Q +GINAVLYYAP++F+N G ++QT+ +GVVN IFT++A VDRFGRKPLLI G Sbjct: 299 QAIGINAVLYYAPRIFENAG-AEGGGMMQTVIMGVVNIIFTLVAIFTVDRFGRKPLLIIG 357 Query: 340 ALGMAAMMAVLGCCFWFKVGGVLPLASVLLYIAVFGMSWGPVCWVVLSEMFPSSIKGAAM 399 ++GMA + C + GVLP+ S+++Y A F MSWGP+CWV++SE+FP++I+G A+ Sbjct: 358 SIGMAVGAFAVAMCDSMAIKGVLPVLSIIVYAAFFMMSWGPICWVLISEIFPNTIRGKAV 417 Query: 400 PIAVTGQWLANILVNFLFKVADGSPALNQTFNHGFSYLVFAALSILGGLIVARFVPETKG 459 IAV QW+ N +V+ F PAL F+ F+Y ++ + + + V R+VPETKG Sbjct: 418 AIAVAFQWIFNYIVSSTF------PAL-YDFSPMFAYSLYGIICVAAAIFVWRWVPETKG 470 Query: 460 RSLDEIEEMWRSQK 473 ++L+++ ++W+ K Sbjct: 471 KTLEDMSKLWKKNK 484 Lambda K H 0.327 0.140 0.434 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: 536 Number of extensions: 27 Number of successful extensions: 7 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: 473 Length of database: 484 Length adjustment: 34 Effective length of query: 439 Effective length of database: 450 Effective search space: 197550 Effective search space used: 197550 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 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