Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate WP_085219145.1 B9N75_RS12805 ABC transporter ATP-binding protein
Query= uniprot:D8IUD1 (522 letters) >NCBI__GCF_900177405.1:WP_085219145.1 Length = 311 Score = 96.7 bits (239), Expect = 1e-24 Identities = 77/232 (33%), Positives = 126/232 (54%), Gaps = 36/232 (15%) Query: 12 PLLTLSGIGKRYAAPV--LDGIDLDLRPGQVLALTGENGAGKSTLSKIICGLVDASAGGM 69 P+L+++ + K YA+ + L+ + LD+R G++ AL G NGAGK+TL I+CG+V + G + Sbjct: 3 PVLSIASLSKTYASGLTALNDVSLDIRKGEIFALLGPNGAGKTTLISIVCGIVTPTGGTV 62 Query: 70 MLDGQPYAPASRTQAEGLGIRMVMQELN------LIPTLSIAENLFLEKLPRRFGWIDRK 123 ++DG A R +G +V QEL+ + T++ + LF K P Sbjct: 63 LVDGVDAARDFRMARTRIG--LVPQELHTDSFETVWATVTFSRGLF-GKPP--------- 110 Query: 124 KLAEAARAQMEVVGLGELDPW----TPVGDLGLGHQQMVEIARNLIGSCRCLILDEPTAM 179 + A +E V L +L W + + +L G ++ V IA+ L L LDEPTA Sbjct: 111 -----SPAHVEKV-LKDLSLWDKRKSKIQELSGGMKRRVMIAKALSHEPDILFLDEPTAG 164 Query: 180 LTNREVEL---LFSRIERLRAEGVAIIYISHRLEELKRIADRIVVLRDGKLV 228 + +VEL +++ + RLR GV II +H +EE + +ADR+ V+ G+L+ Sbjct: 165 V---DVELRRDMWALVHRLREGGVTIILTTHYIEEAEEMADRVGVISKGELI 213 Score = 65.1 bits (157), Expect = 4e-15 Identities = 50/226 (22%), Positives = 100/226 (44%), Gaps = 22/226 (9%) Query: 264 PVLRIRGLGRA-----PVVHPASLALHAGEVLGIAGLIGSGRTELLRLIFGADRAEQGEI 318 PVL I L + ++ SL + GE+ + G G+G+T L+ ++ G G + Sbjct: 3 PVLSIASLSKTYASGLTALNDVSLDIRKGEIFALLGPNGAGKTTLISIVCGIVTPTGGTV 62 Query: 319 FIGDSQEPARIRSPKDAVKAGIAMVTEDRKGQGLLLPQAISVNTSLANLGSVS-RGGMLD 377 + R + + L+PQ + ++ +V+ G+ Sbjct: 63 LVDGVDAARDFRMARTRIG---------------LVPQELHTDSFETVWATVTFSRGLFG 107 Query: 378 HAAESSVAQDYVKKLRIRSGSVAQAAGELSGGNQQKVVIARWLYRDCPIMLFDEPTRGID 437 + + +K L + ++ ELSGG +++V+IA+ L + I+ DEPT G+D Sbjct: 108 KPPSPAHVEKVLKDLSLWDKRKSKIQ-ELSGGMKRRVMIAKALSHEPDILFLDEPTAGVD 166 Query: 438 IGAKSDIYRLFAELAAQGKGLLVVSSDLRELMQICDRIAVMSAGRI 483 + + D++ L L G +++ + + E ++ DR+ V+S G + Sbjct: 167 VELRRDMWALVHRLREGGVTIILTTHYIEEAEEMADRVGVISKGEL 212 Lambda K H 0.320 0.137 0.390 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: 366 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: 522 Length of database: 311 Length adjustment: 31 Effective length of query: 491 Effective length of database: 280 Effective search space: 137480 Effective search space used: 137480 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 (21.8 bits) S2: 50 (23.9 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