Align Inositol transport system ATP-binding protein (characterized)
to candidate AZOBR_RS31880 AZOBR_RS31880 sugar ABC transporter ATP-binding protein
Query= reanno::Phaeo:GFF717 (261 letters) >FitnessBrowser__azobra:AZOBR_RS31880 Length = 515 Score = 155 bits (392), Expect = 2e-42 Identities = 89/240 (37%), Positives = 136/240 (56%), Gaps = 5/240 (2%) Query: 7 LIRMQGIEKHFGSVIALAGVSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDILF 66 ++R+ GI K FG ++A +S+ + GE LLG+NGAGK+T + + G + +G I Sbjct: 7 VLRLSGITKRFGPLVANDSISLTLHKGEVLALLGENGAGKTTLMNILFGHYVADEGSIEA 66 Query: 67 EGQPLHFADPRDAIAAGIATVHQHLAMIPLMSVSRNFFMGNEPIRKIGPLKLFDHDYANR 126 GQPL PR A+AAGI VHQH + +SV N +G E + + D A Sbjct: 67 FGQPLPPGSPRAALAAGIGMVHQHFTLADNLSVLDNIAVGTESLWR----PRSDRAAAKA 122 Query: 127 ITMEEMRKMGINLRGPDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALGVRQTAN 186 ++ R+ G+ +R PD VG LS GERQ I +A++ A+VLILDEPT+ L +++A+ Sbjct: 123 KLLDLARRFGLEVR-PDALVGDLSVGERQRAEILKALYRDARVLILDEPTAVLTPQESAS 181 Query: 187 VLATIDKVRKQGVAVVFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEELQDMMAG 246 + T+ ++ G+AVVFI+H + A D VL G+ + T + + EEL ++M G Sbjct: 182 LFDTLRRLTADGLAVVFISHKMNEVFAASDTVAVLRGGRLVATRKTAETDREELAELMVG 241 Score = 78.2 bits (191), Expect = 3e-19 Identities = 59/250 (23%), Positives = 108/250 (43%), Gaps = 4/250 (1%) Query: 5 QPLIRMQGIEKHFGSVIALA-GVSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGD 63 +P++ + G+ G L GV + V + + G +G G++ + +SG+ P G Sbjct: 256 EPVLTLSGVTVASGHGRPLLDGVDLTVRRRQIVGIAGVSGNGQTALAELISGLIHPDSGT 315 Query: 64 ILFEGQPLHFADPRDAIAAGIATVHQ--HLA-MIPLMSVSRNFFMGNEPIRKIGPLKLFD 120 + +G+ + A+P + + G+A + + H A ++ M+V N L Sbjct: 316 MTLKGEAIGNAEPAEMVRRGVARIPEDRHAAGLVGAMAVWENLIAERYHDPAFQRFGLIR 375 Query: 121 HDYANRITMEEMRKMGINLRGPDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALG 180 A E + + GPD LSGG Q + + R + G +++ +PT L Sbjct: 376 RGAARAYAEEVIAAFDVRCPGPDARTQLLSGGNMQKLILGRTLAHGPDLILASQPTRGLD 435 Query: 181 VRQTANVLATIDKVRKQGVAVVFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEEL 240 V + V + + R G V+ I+ ++ LA+ D TV G+ G +S +L Sbjct: 436 VGAVSYVHGRLLEARAAGAGVLVISEDLDEILALADGITVAYHGRLTPVLPHGRVSVRQL 495 Query: 241 QDMMAGGQEL 250 +MAG E+ Sbjct: 496 GLLMAGHWEI 505 Lambda K H 0.321 0.137 0.395 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: 348 Number of extensions: 18 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 261 Length of database: 515 Length adjustment: 30 Effective length of query: 231 Effective length of database: 485 Effective search space: 112035 Effective search space used: 112035 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 (21.9 bits) S2: 49 (23.5 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