Align phenylacetate-CoA ligase (EC 6.2.1.30) (characterized)
to candidate WP_066607782.1 V473_RS17010 acyl--CoA ligase
Query= BRENDA::D3GE78 (556 letters) >NCBI__GCF_001046645.1:WP_066607782.1 Length = 556 Score = 120 bits (301), Expect = 1e-31 Identities = 140/521 (26%), Positives = 221/521 (42%), Gaps = 48/521 (9%) Query: 57 RLAAGLRKSGLQRGDRVLLFSGNDLFFPVVFLGVIMAGGIFTGANPTFVARELAYQLQDS 116 R A GL+ G+ RGD V + + + F M G + N + A E+AY Q++ Sbjct: 53 RRARGLKALGIGRGDHVGILLPSSIEFVETLFANAMCGAVSVLMNARYKAPEMAYVAQNA 112 Query: 117 GATYLLC---ASNSLETGLEAAK------QAKLPQSHIFAYDTSIYDGVTNPQKGCAYWS 167 ++ S ++ G + A P + A + + + + Sbjct: 113 DLRAIVTNDLISEHVDFGARLTEAFPDLSSAVDPAALTLAETPLLRQIIMLGGRSAPGFI 172 Query: 168 DLL----ASEEEGAAFTWDELSTPALSSTTLALNYSSGTTGRPKGVEISHRNYVA---NM 220 D A++ D T + T + L Y+SGT+ PKG +SH N+ Sbjct: 173 DQAMFDAAADGVSEMDIHDARLTVRVRDTAMIL-YTSGTSANPKGCLLSHEAVTREANNL 231 Query: 221 LQYCHTASLHPDYKARLERSRWLCFLPMYHAMAQNIFIAAALYRATPVYIMSKFDFVKML 280 +Y PD +A W LP++H A + A T + FD + L Sbjct: 232 ARY--RWGFQPDERA------WSP-LPLFHIAAMLCMLGAMDVGGTFIG-QPHFDAGESL 281 Query: 281 EYTQRFRITDFILVPPVVV---ALAKHPAVGQYDLSSVELVGSGAA----PLGREVCEEV 333 + R+T L P V A+ HP + D+SSV L S A +GR ++ Sbjct: 282 RQIEAERVTMMFL--PFVTFHQAMIAHPDWDKTDMSSVRLQNSCFAFMPDRVGRAYRDKA 339 Query: 334 EKLWPPGKINIKQGWGMTEATCSVTGWNPAEISTSA--SVGELNANCEAKIMFDGVEVKE 391 + G + GMTEAT VT PA +G A E KI+ V+ Sbjct: 340 PNMLQVGTM------GMTEATGIVTTGGPAMDPEMGFRKLGYPLAGIEMKIIDPDTGVER 393 Query: 392 R-NSRGELWVRAPNVMKGYWRNEKATKETKTEDGWLLTGDIAFVDDDGKFHVVDRMKELI 450 + RGE+ +R N+ GY+R+ + T E DGW + DI +D +G R K+++ Sbjct: 394 GVDERGEILIRGYNLFDGYYRDPEKTAEAIDPDGWYHSADIGSIDAEGHVMFHGRFKDML 453 Query: 451 KVKGNQVAPAELEALLLEHPAISDVAVIGVVINN-DERPRAYVVLRPGQSATANEIAHYL 509 KV G VA AE+EA+L HPA+ V+G+ + E P AY+ S +E+ Y Sbjct: 454 KVGGENVAAAEVEAVLASHPAVRLAQVVGLPDDRLAEIPAAYIECDGDVSVEPDELIAYT 513 Query: 510 DNKVSAFKRITGGVVFLEAIPKNPSGKILRMKLREQAKEEL 550 ++++FK + + F++ P + S KI + KLR +EL Sbjct: 514 KARLASFK-VPRHIRFVDEWPMSAS-KIQKFKLRAALMDEL 552 Lambda K H 0.319 0.134 0.403 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: 648 Number of extensions: 29 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: 556 Length of database: 556 Length adjustment: 36 Effective length of query: 520 Effective length of database: 520 Effective search space: 270400 Effective search space used: 270400 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: 53 (25.0 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