Align Benzoate--CoA ligase; Benzoyl-CoA synthetase; EC 6.2.1.25 (characterized)
to candidate GFF1013 PGA1_c10300 acetyl-coenzyme A synthetase AcsA
Query= SwissProt::Q8GQN9 (527 letters) >FitnessBrowser__Phaeo:GFF1013 Length = 516 Score = 164 bits (416), Expect = 6e-45 Identities = 140/463 (30%), Positives = 223/463 (48%), Gaps = 33/463 (7%) Query: 72 LQPKDRVLVCVLDGIDFPTTFLGAIKGGVVPIAINTLLTESDYEYMLTDSAARVAVVSQE 131 +QP DRV V + +D L K G + + + L A+R+ E Sbjct: 72 VQPGDRVGVLLSQSVDCAVAHLAIWKIGAISVPLFKLFQHDAL-------ASRIGDAGLE 124 Query: 132 LLPLFAPMLGKVPTL-EHLVVAGGAGEDSLAALLATGSEQFEAAPTRPDDHCFWLYSSGS 190 L+ ++ +L + L+VA D L+A A T P+ +Y+SG+ Sbjct: 125 LVLTDGGGTAQLGSLAQPLLVA-----DILSASTGQSDHLLPYAETTPETPAVLIYTSGT 179 Query: 191 TGAPKGTVHIHSDLIH--TAELYARPILGIREGDVVFSAAKLFFAYGLGNGLIFPLAVGA 248 TG+ KG +H H L + LG + GD +++ A + GL + L+ LA+G Sbjct: 180 TGSAKGALHGHRVLSGHLPGVAISHDHLG-QPGDCLWTPADWAWIGGLFDVLMPGLALGV 238 Query: 249 TAVLMA-ERPTPAAVFERLRRHQPDIFYGVPTLYASMLANPDCPKEGELRLRACTSAGEA 307 V ++ TP A E +R+ + PT + A +G LR+ S GE Sbjct: 239 PVVAARLDKFTPEACAEIIRQGDVRNVFFPPTALRLLKA----AGQGLDGLRSVASGGEP 294 Query: 308 LPEDVGRRWQARFGVDILDGIGSTEMLHIFLSNRAGD--VHYGTSGKPVPGYRLRLIDED 365 L ++ Q GV I + G TE ++ +S+ D V G G+PVPG + ++D+ Sbjct: 295 LGAEMLAWGQRHLGVTINEFYGQTEC-NMTVSSCVADFPVRPGCIGRPVPGCTVEVLDDT 353 Query: 366 GAEITTAGVAGELQISGPSSAVM--YWNNPEKTAATFMGEWTRSGDKYLVNDEGYYVYAG 423 G T G++ + ++++M YWN P+ TA F +W +GD+ + + Y + G Sbjct: 354 G---TPTKDEGDVAVRRGAASMMLEYWNRPDATAEKFHADWLITGDRGIWEGD-YLRFVG 409 Query: 424 RSDDMLKVSGIYVSPIEVESALIAHEAVLEAAVVGWEDEDHLIKPKAFIVLKPGYGAGEA 483 R DD++ +G + P E+E L+ H AV VVG DE KA++VLKPG+ E Sbjct: 410 REDDVITSAGYRIGPAEIEDCLMTHPAVATVGVVGKPDELRTEIVKAYVVLKPGHSPSE- 468 Query: 484 LRTDLKAHVKNLLAPYKYPRWIEFVDDLPKTATGKIQRFKLRS 526 +DL+ +VK+ LA Y YPR +EF+D LP T TGK+ R +L++ Sbjct: 469 --SDLQDYVKSRLAKYSYPREVEFLDALPMTVTGKVIRKELKA 509 Lambda K H 0.319 0.138 0.412 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: 783 Number of extensions: 44 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 527 Length of database: 516 Length adjustment: 35 Effective length of query: 492 Effective length of database: 481 Effective search space: 236652 Effective search space used: 236652 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 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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