Align Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized)
to candidate WP_055444834.1 AMD28_RS14385 sugar ABC transporter ATP-binding protein
Query= SwissProt::Q9F9B0 (260 letters) >NCBI__GCF_001418105.1:WP_055444834.1 Length = 506 Score = 122 bits (306), Expect = 1e-32 Identities = 72/221 (32%), Positives = 125/221 (56%), Gaps = 9/221 (4%) Query: 7 LTARGLVKRYGRVTALDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPDEGEIRLE 66 L G+ K +G V+ L + + GEI A++G+NGAGKS++IK +SG D G + L+ Sbjct: 10 LEMTGISKSFGVVSVLKNVNLKVKSGEIHALLGENGAGKSTLIKILSGVHQKDTGTVVLD 69 Query: 67 GKPIQFRSPMEARQAGIETVYQNLALSPALSIADNMFLGREIRKPGIMGKWFRSLDRAAM 126 G+ I ++ E + GI VYQ L+L LS+A+N++L K G W ++ + Sbjct: 70 GQEITPKNTHEGQVLGINVVYQELSLVNDLSVAENIYL----HKLGANKTW---MNWKGL 122 Query: 127 EKQARAKLSELGLMTIQNINQAVETLSGGQRQGVAVARAAAFGSKVVIMDEPTAALGVKE 186 K A+ L L N + V+ LS Q+Q V +A+A + +K++I+DEPT K+ Sbjct: 123 IKDAQELLDSLDFKI--NASAKVKDLSIVQKQVVEIAKAISEDTKILILDEPTTVFDPKD 180 Query: 187 SRRVLELILDVRRRGLPIVLISHNMPHVFEVADRIHIHRLG 227 +++ ++ ++ +G I+ ISH++ +F++AD + + R G Sbjct: 181 VKKLFNILFKLKEKGTSIIYISHHLDEIFKIADSVTVLRDG 221 Score = 90.9 bits (224), Expect = 5e-23 Identities = 68/233 (29%), Positives = 116/233 (49%), Gaps = 17/233 (7%) Query: 1 MAQEPILTARGLVKRYGRVTALDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPDE 60 + + PI + L + T + F + PGE+L + G G+G++ K I GA Sbjct: 257 IGEVPIFEVKNLT---AKDTMVHDVSFHVKPGEVLGIAGLGGSGRTETAKLIFGADKKKS 313 Query: 61 GEIRLEGKPIQFRSPMEARQAGIETVYQNLALSPALSIADNMFLGREIRKPGIMGKWFRS 120 G + LEGK I SP++A + I V ++ + +FL IR+ I F S Sbjct: 314 GTLILEGKEIVTNSPVDAARYQIGFVSEDRK-------EEGVFLPLSIRR-NISVTSFDS 365 Query: 121 LDRAA----MEKQARAKLSELGLMTIQNINQA--VETLSGGQRQGVAVARAAAFGSKVVI 174 + +E + + L + + I+ N V+ LSGG +Q VA+A+ + SKV+ Sbjct: 366 ISSKLGFINVESEYKKVLGLIEKLNIKTPNSEINVKNLSGGNQQKVALAKWLSIESKVIF 425 Query: 175 MDEPTAALGVKESRRVLELILDVRRRGLPIVLISHNMPHVFEVADRIHIHRLG 227 +DEPT + V + +LI +V ++G+ +V+IS +MP + ++DRI + G Sbjct: 426 IDEPTRGVDVGAKIEIYKLINEVAKKGVGVVVISSDMPEIMGISDRILVMHEG 478 Lambda K H 0.321 0.136 0.383 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: 268 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: 260 Length of database: 506 Length adjustment: 29 Effective length of query: 231 Effective length of database: 477 Effective search space: 110187 Effective search space used: 110187 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: 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