Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_013645675.1 METBO_RS10410 AMP-binding protein
Query= BRENDA::A4YDR9 (549 letters) >NCBI__GCF_000191585.1:WP_013645675.1 Length = 552 Score = 196 bits (498), Expect = 2e-54 Identities = 158/552 (28%), Positives = 263/552 (47%), Gaps = 48/552 (8%) Query: 27 FLERAGKYFKDKTAVVY--RDSRYTYSTFYDNVMVQASALMRRGFSREDKLSFISRNRPE 84 F E+ + + +VY RD R+TY F + V + A L+ G + D + ++N P+ Sbjct: 11 FFEKQVEKDPSRDFLVYPDRDLRFTYKQFDERVNMLAKGLLSIGVKKGDHVGIWAKNVPD 70 Query: 85 FLESFFGVPYAGGVLVPINFRLSPKEMAYIINHSDSKFVVV-----DEPYLNSLLEVKDQ 139 +L F G VLV +N E+ Y++ SD K + + D YL L ++ + Sbjct: 71 WLTFMFATAKIGVVLVTMNTAYKSHELEYVLKQSDMKALAIIDGFRDVDYLKILYDLVPE 130 Query: 140 IKA----EIILLEDPDNPSASETARKEVRMTYRE---LVKGGSRDPLPI----PAKEEYS 188 ++ E+ P +++ R Y ++ G D + + Sbjct: 131 LRTHERGELKSERFPYLKQVIYVGQEKHRGMYNTNELMLLGKHTDDTEFLRVKKTLDNHD 190 Query: 189 MITLYYTSGTTGLPKGVMHHHRGAFLNAMAEVLEHQMDLNSVYLWTLPMFHAASWGFSWA 248 +I + YTSGTTG PKGVM HR N + +P+FH +G Sbjct: 191 VINMQYTSGTTGFPKGVMLTHRNILNNGYYIGECQKFTEEDKLCLPVPLFHC--FGIVLG 248 Query: 249 TVAV---GATNVCLDKVDYPLIYRLVEKERVTHMCAAPTVYVNLADYMKRNNLKFSNRVH 305 +A+ T V L++ D L V+KE T + PT+++ ++ ++ Sbjct: 249 VLAILTHRGTLVMLEEFDPLLALAAVQKESCTALYGVPTMFIAEFNHPMFEMFDLTSLRT 308 Query: 306 MLVAGAAPAPATLKAMQEIGGYMCHVYGLTETYGPHSICEWRREWDSLPLEEQAKLKARQ 365 ++AG+ P ++AM+++ M H+ +T YG + E + +++ + + Sbjct: 309 GIMAGS---PCPIEAMKKVISDM-HMEDITIAYG---LTEASPVFTQTSVDDSVEKRVNT 361 Query: 366 -GIPYVSFEMDVFDANGKPVPWDGKTIG-----EVVMRGHNVALGYYKNPEKTAESFR-D 418 G + E+ + D P G+T+G E+ RG+NV GYYK P+KT E+ D Sbjct: 362 VGRARPNIEVKLID------PETGETLGPGQPGEICCRGYNVMKGYYKMPDKTKEAIEED 415 Query: 419 GWFHSGDAAVVHPDGYIEIVDRFKDLINTGGEKVSSILVEKTLMEIPGVKAVAVYGTPDE 478 GW HSGD A V DGY IV R KD+I GGE + +E+ + +P V+ V V G PDE Sbjct: 416 GWLHSGDLATVDKDGYYTIVGRIKDMIIRGGENIYPREIEEFIHTMPEVQDVQVVGIPDE 475 Query: 479 KWGEVVTARIELQEGVKLTEEEVIKFCKERLAHFECPK---IVEFGPIPMTATGKMQKYV 535 K+GE+V A + ++ V L EE+V + +++A ++ PK IVE P+T +GK+QK+ Sbjct: 476 KYGEIVGAFVIPEKDVDLEEEDVRDYALQKIARYKVPKHVFIVE--EFPLTTSGKIQKFK 533 Query: 536 LRNEAKAKANKE 547 LR++A N++ Sbjct: 534 LRDQAVELLNEK 545 Lambda K H 0.319 0.136 0.411 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: 698 Number of extensions: 42 Number of successful extensions: 6 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: 549 Length of database: 552 Length adjustment: 36 Effective length of query: 513 Effective length of database: 516 Effective search space: 264708 Effective search space used: 264708 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 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