Align ABC-type sugar transport system, ATP-binding protein; EC 3.6.3.17 (characterized, see rationale)
to candidate WP_058930145.1 AU252_RS07280 sugar ABC transporter ATP-binding protein
Query= uniprot:A0A0C4Y5F6 (540 letters) >NCBI__GCF_001484605.1:WP_058930145.1 Length = 506 Score = 348 bits (892), Expect = e-100 Identities = 199/496 (40%), Positives = 298/496 (60%), Gaps = 11/496 (2%) Query: 4 MSDTSTKAPLLALRNICKTFPGVRALRKVELTAYAGEVHALMGENGAGKSTLMKILSGAY 63 M + PLL +R + K F GV+AL+ V+L GEVH +MG+NGAGKSTL+K LSG + Sbjct: 1 MFEEDQPRPLLEVRGLTKRFAGVQALKGVDLQVLPGEVHCVMGQNGAGKSTLIKTLSGVH 60 Query: 64 TADPGGECHIDGQRVQIDGPQSARDLGVAVIYQELSLAPNLSVAENIYLGRALQRRGLVA 123 D GGE +G+++ + P +A DLG+A +YQEL + LSVAENI+LG G++ Sbjct: 61 QPD-GGEIRWEGKQITLPRPTAALDLGIATMYQELDVVDGLSVAENIFLGHERSTGGVLH 119 Query: 124 RGDMVRACAPTLARLG-ADFSPAANVASLSIAQRQLVEIARAVHFEARILVMDEPTTPLS 182 L RLG SP+ V +LS A +Q+V +ARA+ + ++++MDEP+ L Sbjct: 120 VKKTNAIARTLLKRLGHGSLSPSTEVGTLSAANKQIVSMARALSRDTKLIIMDEPSAILD 179 Query: 183 THETDRLFALIRQLRGEGMAILYISHRMAEIDELADRVTVLRDGCFVGT-LDRAHLSQAA 241 + E LF ++R+L +G+A++YISHR+ EI ++ DR++V++DG L ++ Sbjct: 180 SGEVSNLFRVVRELTAQGIAVVYISHRLEEIRQIGDRISVIKDGRSTANGLSVTDTQKSE 239 Query: 242 LVKMMVGRDLSGFYTKTHGQAVEREVMLSVRDVADGRRVKGCSFDLRAGEVLGLAGLVGA 301 L+++M GRD++ + + + V+L V ++ + S +RAGE+LG AGLVG+ Sbjct: 240 LIRLMTGRDVANVFPERKPVPADAPVVLDVDNLELYGHFEKVSLTVRAGEILGFAGLVGS 299 Query: 302 GRTELARLVFGADARTRGEVRIANPAGSGGLVTLPAGGPRQAIDAGIAYLTEDRKLQGLF 361 R+E+ ++GA + G V + A G VT A++AGI E+RK QGL Sbjct: 300 KRSEILETIYGARKASSGRVSVNGKALRPGSVT-------SAVNAGIGLSPEERKSQGLI 352 Query: 362 LDQSVHENINLIVAARDALGLGRLNRTAARRRTTEAIDTLGIRVAHAQVNVGALSGGNQQ 421 LD+ + +N+ L R A +G LN A R E I L +R A LSGGNQQ Sbjct: 353 LDEPLFKNVTLSTFERFAR-MGYLNEAAERNAAREQIAALELRPADPDRPARTLSGGNQQ 411 Query: 422 KVMLSRLLEIQPRVLILDEPTRGVDIGAKSEIYRLINALAQSGVAILMISSELPEVVGLC 481 K++L+R L VL+LDEPTRGVD+GA+SEIY LI LA++G AI+++SSE+ EV+GL Sbjct: 412 KILLARWLVHGTSVLLLDEPTRGVDVGARSEIYDLIRKLAEAGTAIIVVSSEIEEVLGLA 471 Query: 482 DRVLVMREGTLAGEVR 497 D VLV+ +G + + + Sbjct: 472 DNVLVIDDGKVLTQTK 487 Lambda K H 0.320 0.136 0.382 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: 602 Number of extensions: 37 Number of successful extensions: 9 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: 540 Length of database: 506 Length adjustment: 35 Effective length of query: 505 Effective length of database: 471 Effective search space: 237855 Effective search space used: 237855 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 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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