Align Inositol transport system ATP-binding protein (characterized)
to candidate WP_085544213.1 B9Y55_RS04705 ABC transporter ATP-binding protein
Query= reanno::Phaeo:GFF717 (261 letters) >NCBI__GCF_900177735.1:WP_085544213.1 Length = 505 Score = 172 bits (435), Expect = 2e-47 Identities = 85/239 (35%), Positives = 140/239 (58%), Gaps = 5/239 (2%) Query: 8 IRMQGIEKHFGSVIALAGVSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDILFE 67 + ++G+ K FG +A+ +SVD+ G H ++G+NGAGKST +K + G+H P +G+I + Sbjct: 4 LSIKGLTKTFGPFVAVDDISVDIKGGTIHAVVGENGAGKSTIMKCIYGIHHPDRGEISMD 63 Query: 68 GQPLHFADPRDAIAAGIATVHQHLAMIPLMSVSRNFFMGNEPIRKIGPLKLFDHDYANRI 127 G+PL+ PRDA+A+GI VHQH ++P MSV RN +G+EP++ + FD + A Sbjct: 64 GKPLYIRSPRDAMASGIGMVHQHFMLVPSMSVCRNVVLGDEPVKGLA----FDLNRARSE 119 Query: 128 TMEEMRKMGINLRGPDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALGVRQTANV 187 + G+++ PD VGTL G +Q V I + ++ A+VLI DEPT+ L ++ + Sbjct: 120 VFRLIELYGLDI-SPDVPVGTLPVGLQQQVEILKLLYRQAEVLIFDEPTAVLSPKEVGRL 178 Query: 188 LATIDKVRKQGVAVVFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEELQDMMAG 246 T+ + G V+FI HN+ L + D +V+ +G + T ++ L ++M G Sbjct: 179 FETLRGFKDAGKTVIFIAHNLGEVLDISDNISVMRKGSLIDTRPASELDKSSLAELMVG 237 Score = 78.2 bits (191), Expect = 3e-19 Identities = 65/256 (25%), Positives = 120/256 (46%), Gaps = 12/256 (4%) Query: 6 PLIRMQGIEKHFGSVIALAGVSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDIL 65 PL+ + GI S L VS+ + GE + G G G+S + +SG+ + + G ++ Sbjct: 255 PLLELSGISVAGDSRPLLDDVSLKIHGGEVLGVAGITGNGQSELEEVISGLRE-SDGTVV 313 Query: 66 FEGQPLHFADPRDAIAAGIATVHQH---LAMIPLMSVSRNFFMGNEPIRKI--GPLKLFD 120 +G L +D +G+A + + + PL S++ N MG + + GP + Sbjct: 314 IDGVDLTSSDSHRRRESGLAYIPEDRLKTGLAPLASLADNGLMGYQYQDRFRNGPFQ--- 370 Query: 121 HDYANRITMEE--MRKMGINLRGPDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSA 178 + A ++ + M K G+ GTLSGG Q + + R + KVL++ +PT Sbjct: 371 -NRAESLSHIDGIMDKYGVAAAHRAVQSGTLSGGNMQRLVMGRELEHDPKVLVVSQPTRG 429 Query: 179 LGVRQTANVLATIDKVRKQGVAVVFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAE 238 + + + I +R +G AV+ I+ ++ L++ DR V+ RGK + + + + Sbjct: 430 VDIGGAEEIHRHILDLRSRGSAVLLISSDLEEVLSLSDRVAVMFRGKIVALLSSKEATRD 489 Query: 239 ELQDMMAGGQELATLE 254 + +M G+E LE Sbjct: 490 RVGRIMLEGEEGGDLE 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: 369 Number of extensions: 17 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 261 Length of database: 505 Length adjustment: 29 Effective length of query: 232 Effective length of database: 476 Effective search space: 110432 Effective search space used: 110432 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 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