Align ABC transporter related; Flags: Precursor (characterized, see rationale)
to candidate WP_009141256.1 HMPREF9452_RS06110 ABC transporter ATP-binding protein
Query= uniprot:B2T9V9 (510 letters) >NCBI__GCF_000225705.1:WP_009141256.1 Length = 508 Score = 267 bits (682), Expect = 8e-76 Identities = 162/486 (33%), Positives = 266/486 (54%), Gaps = 6/486 (1%) Query: 20 VTKRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILTGLRKPDTGEVRFSGAAAP 79 + K FGS AL+ V + V G HA++G NGAGKSTL+++L GL + + GE+ G Sbjct: 14 IVKMFGSFCALDHVDLDVERGSIHAILGENGAGKSTLMNVLYGLYQAEEGEIFLGGEKVS 73 Query: 80 SIADRDAWRERVACVYQHSTIIRDLSVAENLFINRQPLRG-GVIDWQAMRRDARALLDHW 138 DA + V+QH ++ + +V +N+ + ++P RG G++D +A + R ++ + Sbjct: 74 ISNPNDAIAHGIGMVHQHFMLVDNFTVTQNIILGQEPCRGAGLLDMKAAGQRVRDIIAEY 133 Query: 139 KIDVREDARAGDLSVEARQLVEIARALSYGARFIILDEPTAQLDGDEIKRLFRRISELQR 198 ++V DA+ D+SV +Q VEI +AL GA +ILDEPTA L EI RL + + L Sbjct: 134 GLEVDPDAKIEDISVGMQQRVEILKALYRGADILILDEPTAVLTPQEIDRLVQIMRGLAA 193 Query: 199 EGVTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPREQLIEAMTGERGGLAVADA 258 +G T + I+H L+E+ T++R +++ + V+ + E+L E M G L V A Sbjct: 194 KGKTIIIITHKLKEIKASSDTCTIIRRGKYVGAVDVAGVDEEELAEKMVGHHVNLVVEKA 253 Query: 259 AARGALPADTAVALELKELTGAD-YEGVSFTVKRGEVVGLTGATSSGRTSVAEAIAGLRA 317 A L +K+ G + ++ +V GE+VG+ G +G+ + EAI L Sbjct: 254 PANPGKEVFRIDDLVVKDERGIEAVRHLNLSVCAGEIVGIAGIDGNGQKELVEAITCLTR 313 Query: 318 AKRGTISVDGAILPPGDVPASLAHGIGCVPKDRHHEGLVLTQSVAENASMTIARV--LGK 375 A+ GTI+V+G + + H + + +DR GLVL +VAENA + R G+ Sbjct: 314 AQSGTITVNGEEIQNTTPRNVIDHKVSTIHEDRQRRGLVLPFTVAENAVLEKYRTPEFGE 373 Query: 376 FGIAAPAKKNAFGQKMIDALGI-VAQGPEHVVSGLSGGNQQKVVMARALATNPNVLVLID 434 G+ AK + F +++I + A +H +GLSGGNQQKV++ R ++ NP+VL+ + Sbjct: 374 HGVLDRAKMHEFTEQLIHDYDVRPADCADHTAAGLSGGNQQKVIIGREISNNPDVLIAVQ 433 Query: 435 PTAGVDVKSKEALLSVVDRVREEGKAVLVVSGELDD-LRTCDRVLVMFRGRVAAEFPAGW 493 PT G+DV + E + + R+ G A+L++S ELD+ + D + V++ G + F G Sbjct: 434 PTRGLDVGAIEYVHKTLVAERDRGTAILLISLELDEVMSVADTIAVIYAGAIVDTFKQGD 493 Query: 494 QDHDLI 499 D + I Sbjct: 494 VDENRI 499 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: 588 Number of extensions: 30 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: 510 Length of database: 508 Length adjustment: 34 Effective length of query: 476 Effective length of database: 474 Effective search space: 225624 Effective search space used: 225624 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