Align Inositol transport system ATP-binding protein (characterized)
to candidate WP_068009665.1 PsAD2_RS19320 ATP-binding cassette domain-containing protein
Query= reanno::Phaeo:GFF717 (261 letters) >NCBI__GCF_001623255.1:WP_068009665.1 Length = 497 Score = 144 bits (364), Expect = 3e-39 Identities = 80/240 (33%), Positives = 138/240 (57%), Gaps = 5/240 (2%) Query: 7 LIRMQGIEKHFGSVIALAGVSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDILF 66 L+ +QGIEK F + L V + + G L G+NGAGKST +K +SG+++ G + + Sbjct: 4 LLELQGIEKSFSGINVLKSVDLTIRAGRVVALAGENGAGKSTLMKIISGIYQRDAGTVFY 63 Query: 67 EGQPLHFADPRDAIAAGIATVHQHLAMIPLMSVSRNFFMGNEPIRKIGPLKLFDHDYANR 126 +G + F + R+++ AGI +HQ L ++P +SV+ N ++G EP K+G ++ D R Sbjct: 64 KGHEVEFTNARESMDAGIGIIHQELNLLPDLSVAENIYLGREP-TKLGKIQ---WDVVQR 119 Query: 127 ITMEEMRKMGINLRGPDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALGVRQTAN 186 + + + ++ ++ P +G LS ++Q V IA+A+ A+V+I+DEPT AL +TA Sbjct: 120 ESKKYLAQLKQDI-DPTTPLGKLSIAQQQMVEIAKALSLNAEVIIMDEPTDALTDIETAI 178 Query: 187 VLATIDKVRKQGVAVVFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEELQDMMAG 246 + +D++R QG +VFI+H + + D +L G+ + DIS ++L M G Sbjct: 179 LFEVVDELRAQGKGLVFISHRLGEIFQMCDDIAILRDGQMVHQGAVADISEDDLIRHMVG 238 Score = 82.4 bits (202), Expect = 2e-20 Identities = 57/226 (25%), Positives = 100/226 (44%), Gaps = 4/226 (1%) Query: 26 VSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDILFEGQPLHFADPRDAIAAGIA 85 +S GE G GAG++ K + G + G + +GQ + P+D + A I Sbjct: 270 ISFTANAGEVVGFAGLVGAGRTELAKAIFGANPIRGGSVKIDGQEISLKSPQDGVKAKIG 329 Query: 86 TV---HQHLAMIPLMSVSRNFFMGNEPIRKIGPLKLFDHDYANRITMEEMRKMGINLRGP 142 V + ++ S+ N + R L + + E + I R Sbjct: 330 YVTEDRKQEGLVQSQSLGSNMSLTGLD-RFCNTLGIVNKTSEAVTISEYIEAFAIKTRDA 388 Query: 143 DQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALGVRQTANVLATIDKVRKQGVAVV 202 + LSGG +Q V+IA+++ +VLILDEPT + V + I+K++ +G+ ++ Sbjct: 389 STIISNLSGGNQQKVSIAKSLVPEPEVLILDEPTRGVDVGAKREIYTLINKLKAEGLCIL 448 Query: 203 FITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEELQDMMAGGQ 248 I+ ++ L + DR VL+ GK G+ R + + E + GQ Sbjct: 449 LISSDMPELLGISDRILVLSDGKLTGSFDRDEATQENIMRCAVAGQ 494 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: 280 Number of extensions: 12 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: 497 Length adjustment: 29 Effective length of query: 232 Effective length of database: 468 Effective search space: 108576 Effective search space used: 108576 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