Align Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized)
to candidate WP_027178119.1 G496_RS0103835 ABC transporter ATP-binding protein
Query= SwissProt::Q9F9B0 (260 letters) >NCBI__GCF_000429985.1:WP_027178119.1 Length = 513 Score = 144 bits (362), Expect = 5e-39 Identities = 82/226 (36%), Positives = 132/226 (58%), Gaps = 11/226 (4%) Query: 2 AQEPILTARGLVKRYGRVTALDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPDEG 61 + PI++ +G+ KR+G+V A ++ DLYPG I A++G+NGAGKS+++ ++G PDEG Sbjct: 20 SSSPIVSLKGITKRFGKVVANNKIVLDLYPGRIKALLGENGAGKSTLMSMLAGRFQPDEG 79 Query: 62 EIRLEGKPIQFRSPMEARQAGIETVYQNLALSPALSIADNMFLGREIRKPGIMGKWFRSL 121 I ++GK + F S +A AGI VYQ+ L ++++ +N+ LG+E G +F + Sbjct: 80 HIEVDGKRVDFSSSKDAINAGIGMVYQHFMLVDSMTVTENVLLGQE-------GGFFVNP 132 Query: 122 DRAAMEKQARAKLSELGLMTIQNINQAVETLSGGQRQGVAVARAAAFGSKVVIMDEPTAA 181 + + A+ EL + INQ LS G++Q V + + S+V+I DEPTA Sbjct: 133 KEMSRRVKKLAEDYELEIDPDARINQ----LSMGEKQRVEILKLLYRESRVLIFDEPTAV 188 Query: 182 LGVKESRRVLELILDVRRRGLPIVLISHNMPHVFEVADRIHIHRLG 227 L +E+ R+ E + + R+G IV ISH + V +AD + I R G Sbjct: 189 LTPRETFRLFEALWAMTRQGKSIVFISHKLEEVMAIADEVAILRRG 234 Score = 53.9 bits (128), Expect = 7e-12 Identities = 51/235 (21%), Positives = 104/235 (44%), Gaps = 11/235 (4%) Query: 22 LDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPDEGEIRLEGKP-IQFRSPMEARQ 80 L + +++ GE++ ++G G G+ ++++ + G P + + + GK +F + M Sbjct: 286 LKNINIEVHRGEVVGIVGVAGNGQQALVEGVCGLRMPPKDSVFIMGKAWREFFAKMTWNH 345 Query: 81 --AGIETVYQNLALSPALSIADNMFLGREIRKPGIMGKWFRSLDRAAMEKQARAKLSELG 138 + I +LA + L + DN+ L + G D+AA + KL E Sbjct: 346 SLSYIPEDRLDLATARELDLVDNLLL---TTRQGFCSGPVLHRDKAA---EVAKKLVEDH 399 Query: 139 LMTIQNINQAVETLSGGQRQGVAVARAAAFGSKVVIMDEPTAALGVKESRRVLELILDVR 198 + I LSGG Q + +AR +++ ++PT L + + V +L+ R Sbjct: 400 DVRPGRIQALAWQLSGGNLQKLVLARELYREPHLIVAEQPTQGLDISATEEVWNRLLEAR 459 Query: 199 RRGLPIVLISHNMPHVFEVADRIHIHRLGRRLCVINPKDYTMSDAVA-FMTGAKE 252 + ++L++ ++ +++DRI + G + + D D V M G +E Sbjct: 460 KMA-GVLLVTGDLNEALQLSDRIAVMYRGEIMDQFSVNDTEKVDKVGLMMAGVRE 513 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: 280 Number of extensions: 12 Number of successful extensions: 3 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: 260 Length of database: 513 Length adjustment: 29 Effective length of query: 231 Effective length of database: 484 Effective search space: 111804 Effective search space used: 111804 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 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