Align deoxynucleoside transporter, ATPase component (characterized)
to candidate WP_004129793.1 RHSP_RS32525 sugar ABC transporter ATP-binding protein
Query= reanno::Burk376:H281DRAFT_01113 (515 letters) >NCBI__GCF_000359745.1:WP_004129793.1 Length = 527 Score = 339 bits (870), Expect = 1e-97 Identities = 201/485 (41%), Positives = 288/485 (59%), Gaps = 13/485 (2%) Query: 21 VHKRFTGVHALRGVSLSFQRGQIYHLLGENGCGKSTLIKIISGAQPPDEGQLVIEGVPHA 80 V K F GVHALRGVSL+ Q G I+ L+GENG GKSTL+KI+ G P EG + + G + Sbjct: 18 VRKSFGGVHALRGVSLTIQPGTIHALVGENGAGKSTLLKILQGVVTPTEGSIEVFGEHMS 77 Query: 81 RLSALEALAAGIETVYQDLSLLPNMSVAENVALTSELATHEGRLARTFDRRVLAATAARA 140 S + GIE ++QDLSL+P ++VA+N+ L E RL+ D R A AA Sbjct: 78 SSSPENSRRLGIEMIFQDLSLIPTLTVAQNIFLNRE----PRRLSILVDERREIAQAAEI 133 Query: 141 LEAVGLPGNSEFQSTLIEQLPLATRQLVAIARAIASEAKFVIMDEPTTSLTQKEVDNLIA 200 + + L + T + +L QL IA+AI +A+ +I+DEPT+SL+ +E D L Sbjct: 134 IGQLNLRVDPR---TPVFELSPGQAQLTEIAKAIHQDARILILDEPTSSLSAQEADTLFG 190 Query: 201 VLANLRAQGVTVLFVSHKLDECYAIGGEVIVLRDGQKMAQGPIAEFTKAQISELMTGRHL 260 +L L A G V++VSH++ E I E+ +LRDGQ + G +EFT I + M G+ + Sbjct: 191 MLKKLTAAGTAVIYVSHRMSEIMTIADEITILRDGQNVTSGKTSEFTLDSIVQHMVGKRV 250 Query: 261 SNERYRESA--HAQDIVLDVRGFTR-AGQFSDVSFKLHGGEILGVTGLLDSGRNELARAL 317 + +Y+ A + L VRG + +G+ SDVSF +H GEI+G+ GL+ +GR+ELAR L Sbjct: 251 TGFQYQARAIDRSGKPALSVRGLSGPSGKPSDVSFDVHRGEIVGIAGLMGAGRSELARLL 310 Query: 318 AGVAPAQSGDVLLDGQQIALRTPSDAKRHRIGYVPEDRLNEGLFLDKPIRDNVITAMISS 377 GV +G V L + ++PSDA + I VPE R EGL ++ + DN+ I Sbjct: 311 FGVDKKTAGTVELGDTAVEFKSPSDAIKAGIVLVPESRHEEGLVVEHSVGDNLGLPQIGQ 370 Query: 378 L-RDRFGQIDRTRAQALAEQTVKELQIATPGVDKPVQSLSGGNQQRVLIGRWLAIDPRVL 436 L R F IDR R L +K+L+I TP D V++LSGGNQQ+++I +WLAIDP V+ Sbjct: 371 LVRGPF--IDRRREGTLTSDLIKQLRIKTPSADNKVRNLSGGNQQKIVIAKWLAIDPSVV 428 Query: 437 ILHGPTVGVDVGSKDIIYRIMQRLSQRGIGIILISDDLPELLQNCDRILMMKKGHVSAEY 496 IL PT GVD+GSK I +++ ++ G +I+IS + ELL DRIL+M G ++ E Sbjct: 429 ILDEPTAGVDIGSKAEIVELIRSVASSGKSVIVISSEPAELLATSDRILVMNNGRLAREI 488 Query: 497 RADEL 501 DE+ Sbjct: 489 ERDEI 493 Lambda K H 0.319 0.135 0.376 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: 595 Number of extensions: 25 Number of successful extensions: 6 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: 515 Length of database: 527 Length adjustment: 35 Effective length of query: 480 Effective length of database: 492 Effective search space: 236160 Effective search space used: 236160 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 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