Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_008203190.1 ALPR1_RS19255 long-chain fatty acid--CoA ligase
Query= BRENDA::A4YDT1 (564 letters) >NCBI__GCF_000166275.1:WP_008203190.1 Length = 513 Score = 169 bits (429), Expect = 2e-46 Identities = 136/499 (27%), Positives = 247/499 (49%), Gaps = 34/499 (6%) Query: 69 EAKLSYHELSLMSNRVLSTLRKHGLKKGDVVYLMTKVHPMHWAVFLAVIKGGFVMVPSAT 128 + +L++ +++ +N++ ++++K G+KKGD V L P V+ ++K G ++VP + Sbjct: 25 DKRLTFAQINGAANQIANSIQKLGIKKGDRVALSCLNLPYFPMVYFGILKAGAIVVPLSV 84 Query: 129 NLTVAEMKYRFSDLKPSAIISDS------LRASVMEEALGSLKVEKFL-----------I 171 L E++Y + A + E + E+F+ I Sbjct: 85 LLKHDEIEYHLQNSGAKAYFCFEGTPDLPMAKEGYEGFCNTDCCEQFIVISPQMSDPSPI 144 Query: 172 DGKRETWNSLEDESSNAEPEDTRGEDVIINYFTSGTTGMPKRVIHTAVSYPVGSITTASI 231 DG + ++DE T+ +D + +TSGTTG PK + + + ++ + I Sbjct: 145 DGVKALGMLMKDEPPVFSTVVTKSDDTALIIYTSGTTGKPKGAELSHSNLLLNAMLSVKI 204 Query: 232 VGVRESDLHLNLSATGWAKFAWSSFFSP-LLVGATVVGINYEGKLDTRRYLGEVENLGVT 290 + + + D L + + FA + + L VGAT V + + D + G ++ V Sbjct: 205 LSLEKEDTQLIVLPL-FHIFAMTVLMNAGLYVGATSVLLP---RFDASQVFGLMQKHQVN 260 Query: 291 SFCAPPTAWRQFITLDLDQFRFE----RLRSVVSAGEPLNPEVIKIWKDKFNLTIRDFYG 346 F PT + + + +QF + L++ VS G L V++ +K KFN+ I + YG Sbjct: 261 IFAGVPTMYWGLLNFEGEQFDLKGIAKNLKTCVSGGAALPVNVLENFKKKFNVDILEGYG 320 Query: 347 QTETTAMVG-NFPFLKVKPGSMGKPHPLYDIRLLDDEGKEITKPYEVGHITVKLNPRPIG 405 +E + +V N K GS+G P +++++D+EGKE+ E G + + + G Sbjct: 321 MSEGSPVVTFNQKEFGTKAGSVGVPIWGVEVKIVDEEGKELPVG-EKGELIYRGHNVMKG 379 Query: 406 LFLGYSDEKKNMESFREGYYYTGDKAYFDEEGYFYFVGRGDDVIKTSDYRVGPFEVESAL 465 Y++ + + ++ ++G+ Y+GD A DE+G+F+ V R D+I V P E+E + Sbjct: 380 Y---YNNLEASEKTIQDGWLYSGDVAIKDEDGFFFIVDRTKDMIIRKGLNVYPREIEEVM 436 Query: 466 LEHPAVAEAAVVGVPDTVRWQLVKAYIVLKKGYMPSKELAEEIREKMKTLLSPYKVPRII 525 ++H AV+ AV+GVP + +KA +V G+ S+ EE+ K ++ YK PRII Sbjct: 437 MKHEAVSMVAVIGVPAESLGEEIKACVVRNNGFDISE---EELISWTKAHIASYKYPRII 493 Query: 526 EFVDELPKTISGKIRRVEL 544 EF+D LP + +GKI + EL Sbjct: 494 EFLDALPMSATGKILKKEL 512 Lambda K H 0.318 0.137 0.402 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: 608 Number of extensions: 33 Number of successful extensions: 6 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: 564 Length of database: 513 Length adjustment: 35 Effective length of query: 529 Effective length of database: 478 Effective search space: 252862 Effective search space used: 252862 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 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