Align Nucleoside permease; Flags: Precursor (characterized, see rationale)
to candidate H281DRAFT_03110 H281DRAFT_03110 concentrative nucleoside transporter, CNT family
Query= uniprot:A0KU05 (419 letters) >FitnessBrowser__Burk376:H281DRAFT_03110 Length = 425 Score = 468 bits (1203), Expect = e-136 Identities = 232/425 (54%), Positives = 319/425 (75%), Gaps = 12/425 (2%) Query: 3 ILMSLVGVVVLLAIGFLLSNNKKAINLRTVGGALAIQAAFGGFVLYVPVGKDILKSVSDA 62 I +++G+ VLL I F+ S N++AI LRTV AL Q G F+L+VP+GK IL + + Sbjct: 4 IARNVLGIAVLLFIAFIFSTNRRAIRLRTVSSALLAQVCIGAFILFVPLGKTILAAAAAG 63 Query: 63 VSSVIGYAQNGIGFLFGDLANFKL-------GFIFAVNVLPVIVFFSSLIAVLYYLGIMQ 115 V++V+GY GI FLFG L ++ GF+FAV VLP I+F ++LI+VLYYLG+M+ Sbjct: 64 VNNVLGYGNAGIEFLFGGLVQSRMFEVFGNGGFVFAVRVLPAIIFVTALISVLYYLGVMR 123 Query: 116 WIIRIIGGGLQKALGTSRTESMSATANIFVGQTEAPLVVRPFIPTMTQSELFAIMVGGLA 175 WI+ ++G QK LG S+ ES SA IF+GQ+E P VV+PF MT +ELFA+M G+A Sbjct: 124 WIVIVLGTVFQKLLGVSKLESFSAVTTIFLGQSEMPAVVKPFTRDMTGAELFAVMSSGMA 183 Query: 176 SIAGSVLAGYAQMGVPIEYLVAASFMAAPGGLLMAKLMHPETEVAKNDMDELPEDPDKPA 235 ++AGSVLAGYA +GV IEYL+AASFMA PGGLL AK++HP TE ++ +D L D +PA Sbjct: 184 AVAGSVLAGYAGLGVRIEYLLAASFMAVPGGLLFAKIIHPSTEPSRVHLDNLNFDEKRPA 243 Query: 236 NVLDAAAAGASSGMHLALNVGAMLLAFVGLIAMINGIIGGVGGWFGVEGLTLELILGYIF 295 NV++AA++GA+ G+ +A+ VGAML+AFVGLIA++NG++GG+G WFG L+++ +LG +F Sbjct: 244 NVIEAASSGATVGLRIAVMVGAMLIAFVGLIALLNGLVGGIGAWFGHPQLSMQSVLGVVF 303 Query: 296 MPLAFLIGVPWNEALVAGSFIGQKIVVNEFVAYLNFAPYLKDIADGGMIVADTGL-AMTD 354 PLA+LIGVPWNEA++AG+F+GQKI++NEFVAY + +PYLKD A V GL A+ Sbjct: 304 APLAWLIGVPWNEAVIAGNFLGQKIILNEFVAYASLSPYLKDAAS----VTAAGLHALDP 359 Query: 355 RTKAIISFALCGFANLSSIAILLGGLGAMAPNRRHDLAKLGIRAVIAGSLANLMSATIAG 414 RT AI+SFALCGFAN +SIA+L GG A+AP RR ++A+ G+R V+A +L+NLMSATIAG Sbjct: 360 RTIAILSFALCGFANFASIAVLTGGFSAVAPERRAEVARYGLRVVLAATLSNLMSATIAG 419 Query: 415 LFLAI 419 +F+ + Sbjct: 420 MFITL 424 Lambda K H 0.325 0.142 0.407 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: 575 Number of extensions: 23 Number of successful extensions: 3 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: 419 Length of database: 425 Length adjustment: 32 Effective length of query: 387 Effective length of database: 393 Effective search space: 152091 Effective search space used: 152091 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: 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