Align ABC transporter related; Flags: Precursor (characterized, see rationale)
to candidate WP_011914604.1 PST_RS17845 ABC transporter ATP-binding protein
Query= uniprot:B2T9V9 (510 letters) >NCBI__GCF_000013785.1:WP_011914604.1 Length = 525 Score = 203 bits (516), Expect = 1e-56 Identities = 152/504 (30%), Positives = 249/504 (49%), Gaps = 36/504 (7%) Query: 10 SSVPVVEALEVTKRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILTGLRKPDTG 69 S++ ++ V+K F AL+ GE HAL+G NGAGKS+L++I GL P++G Sbjct: 2 SNLNAIQLSGVSKSFDGFMALSQADFTARWGEVHALLGENGAGKSSLMNIAAGLYAPESG 61 Query: 70 EVRFSGAAAPSIADRDAWRERVACVYQHSTIIRDLSVAENLFINRQPLRGGVIDWQAMRR 129 + + A RDA R + V+QH +++ +VAEN+ + P G + R Sbjct: 62 SLLINDNAVRLSGPRDASRYHIGMVHQHFKLVKPFTVAENIQL-ALPEGPGNHAFSGSHR 120 Query: 130 DARALLDH----------WKIDVREDARAGDLSVEARQLVEIARALSYGARFIILDEPTA 179 A L+ + ID R+ + LSV +Q VEI + L GAR +ILDEPTA Sbjct: 121 QRLAALEQRISDKAAELGFSIDPRKITES--LSVAEQQRVEILKVLLAGARILILDEPTA 178 Query: 180 QLDGDEIKRLFRRISELQREGVTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPR 239 L E +RL + R+G + ++H + +V VTV+R R I + + Sbjct: 179 VLTDGEAERLLETVRAFARQGAAVILVTHKMSDVKRFADRVTVMRGGRTIQTLDPQTVSV 238 Query: 240 EQLIEAMTGERGGLAVADAAARGALPADTAVALELKELTGAD----YEGVSFTVKRGEVV 295 +L+ GE + + + A+P + + + TGA GV+ +++ GE+ Sbjct: 239 PELVRLTVGE----SAPASEYQPAIPGEVRLQVRDLRSTGAGGQGVLNGVNLSLRAGEIY 294 Query: 296 GLTGATSSGRTSVAEAIAGLRAAKRGTISVDGAILPPGDVPASLAH-----GIGCVPKDR 350 G+ G +G++ +A + GL GT+ + G GD+ + A I +P DR Sbjct: 295 GIAGVGGNGQSELANVLMGLPEPCDGTLELTGF----GDLRRASAEQRRELRIAAIPADR 350 Query: 351 HHEGLVLTQSVAENASMTIARVLGKFGIAAPAKKNAFGQKMIDAL-GIVAQGPEHV---V 406 + L SVAEN + G++G ++ + +A+ G QG + Sbjct: 351 YGAALAGELSVAENFGVGQVH-SGRYGSFFRLRRKRLEAEAAEAVAGFDVQGVRSLKQKA 409 Query: 407 SGLSGGNQQKVVMARALATNPNVLVLIDPTAGVDVKSKEALLSVVDRVREEGKAVLVVSG 466 + LSGGN QK+V+AR + +P ++++ P+ G+DV++ A+ + + RE G AVLV+S Sbjct: 410 ALLSGGNAQKLVIAREFSRDPLLVLVHSPSRGLDVRATAAVHARLRAAREAGAAVLVISE 469 Query: 467 ELDD-LRTCDRVLVMFRGRVAAEF 489 +LD+ L DR+ VM GR+ AEF Sbjct: 470 DLDEVLALADRIGVMSGGRIVAEF 493 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: 632 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: 510 Length of database: 525 Length adjustment: 35 Effective length of query: 475 Effective length of database: 490 Effective search space: 232750 Effective search space used: 232750 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 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