Align ABC transporter related; Flags: Precursor (characterized, see rationale)
to candidate WP_110805879.1 C8J30_RS10885 sugar ABC transporter ATP-binding protein
Query= uniprot:B2T9V9 (510 letters) >NCBI__GCF_003217355.1:WP_110805879.1 Length = 511 Score = 269 bits (687), Expect = 2e-76 Identities = 166/486 (34%), Positives = 258/486 (53%), Gaps = 9/486 (1%) Query: 22 KRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILTGLRKPDTGEVRFSGAAAPSI 81 K + T AL V + G + LVG NGAGKSTL+ ++ G+ G + G Sbjct: 16 KVYPGTRALKGVDFDLRMGAVNVLVGENGAGKSTLMKLIAGVEDMTEGTITMDGREMRFR 75 Query: 82 ADRDAWRERVACVYQHSTIIRDLSVAENLFINRQPLRGGV-IDWQAMRRDARALLDHWKI 140 DA + V+Q + +LSVAEN+FI + RGG+ ID +A R R L++ + Sbjct: 76 TKADAVAAGIGIVFQELNLFPNLSVAENIFIGHETTRGGIDIDIEAHREATRQLMERLEQ 135 Query: 141 DVREDARAGDLSVEARQLVEIARALSYGARFIILDEPTAQLDGDEIKRLFRRISELQREG 200 ++ D G+L + +Q+VEIA+AL+ AR +ILDEPT+ L E++ LFR I EL +G Sbjct: 136 NIHPDTPLGNLRIGQQQIVEIAKALAQNARILILDEPTSALSAAEVEVLFRVIDELTAQG 195 Query: 201 VTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPREQLIEAMTG----ERGGLAVA 256 V ++ISH L+E+ + +TVLRD + + + +++AM G E G VA Sbjct: 196 VGIVYISHRLEELIRVGDYITVLRDGVITGARSMEGVDIPWIVKAMIGSSSKEYGRSEVA 255 Query: 257 DAAARGALPADTAVALELKELTGADYEGVSFTVKRGEVVGLTGATSSGRTSVAEAIAGLR 316 + D + + G + VS +++ GE+VGL G +GR+ E + Sbjct: 256 NFGPEIFRAEDITLP---RAGGGFTVDHVSLSIRSGEIVGLYGLMGAGRSEFLECVMAQH 312 Query: 317 AAKRGTISVDGAILPPGDVPASLAHGIGCVPKDRHHEGLVLTQSVAENASMTIARVLGKF 376 G V+G L DVP +A GI +P+DR +GL+ S+ EN +++ K Sbjct: 313 PHSGGKFWVEGKPLTERDVPGRIARGIALIPEDRKRDGLIQIMSIRENLTLSSLPSFTKL 372 Query: 377 GIAAPAKKNAFGQKMIDALGIVAQGPEHVVSGLSGGNQQKVVMARALATNPNVLVLIDPT 436 K+ + I L I PE+ VS LSGGNQQKVV+ +AL T P VL++ +P+ Sbjct: 373 FHLDLKKEAKTAVEFIKRLTIKVASPENPVSSLSGGNQQKVVIGKALMTGPKVLLMDEPS 432 Query: 437 AGVDVKSKEALLSVVDRVREEGKAVLVVSGELDD-LRTCDRVLVMFRGRVAAEFPAGWQD 495 G+D+ +K + + R+ EG +L V+ +LD+ L DR++VM +GRV EFP+G + Sbjct: 433 RGIDIGAKAEVFRTMRRLAAEGLGILFVTSDLDEVLALSDRIIVMAQGRVTGEFPSGTEA 492 Query: 496 HDLIAS 501 +I++ Sbjct: 493 AKVISA 498 Lambda K H 0.318 0.134 0.377 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: 578 Number of extensions: 24 Number of successful extensions: 8 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: 510 Length of database: 511 Length adjustment: 35 Effective length of query: 475 Effective length of database: 476 Effective search space: 226100 Effective search space used: 226100 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 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