Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_027720454.1 H589_RS0101900 AMP-binding protein
Query= BRENDA::A4YDR9 (549 letters) >NCBI__GCF_000425265.1:WP_027720454.1 Length = 548 Score = 184 bits (466), Expect = 1e-50 Identities = 149/539 (27%), Positives = 253/539 (46%), Gaps = 38/539 (7%) Query: 28 LERAGKYFKDKTAVVY--RDSRYTYSTFYDNVMVQASALMRRGFSREDKLSFISRNRPEF 85 L+ A + + ++ A+VY RD R TY F + V A LM G + +K++ + N P + Sbjct: 15 LDEAVEKWPEQEAIVYVDRDFRLTYREFGNLVDDLAMGLMALGVKKGEKVAIWATNVPYW 74 Query: 86 LESFFGVPYAGGVLVPINFRLSPKEMAYIINHSDSKFVVVDE-----PYLNS----LLEV 136 + F G +L+ +N E+ Y++ S+ + +V+ + YL + + E+ Sbjct: 75 VALQFATAKIGAILLTVNTFYRTTELEYLLKQSECENLVIIDGFREIDYLQTTYDLIPEL 134 Query: 137 KDQIKAEIILLEDPDNPSASETARKEVRMTYRELVKGGSRDPLPIPAKEE-------YSM 189 + Q + + + PD +++ R Y + EE Y + Sbjct: 135 RTQERGYLKSEKFPDLKRVFFLGQEKHRGMYSMAEVINLSAVVSDEEYEERQTTLNPYDV 194 Query: 190 ITLYYTSGTTGLPKGVMHHHRGAFLNAMAEVLEHQMDLNSVYLWTLPMFHAASWGFS-WA 248 + + YTSGTTG PKGV H N +P+FH A Sbjct: 195 VNMQYTSGTTGFPKGVQLTHYNIGNNGFWIGENQAFQPGDRLCLPVPLFHCFGCVLGVLA 254 Query: 249 TVAVGATNVCLDKVDYPLIYRLVEKERVTHMCAAPTVYVNLADYMKRNNLKFSNRVHMLV 308 V G T V L+ D L+ +++E+ T + PT+++ + D+ +S+ ++ Sbjct: 255 AVNHGTTLVILEGFDPLLVMASIDQEKCTALYGVPTMFIAILDHKLFEKFDYSSLRTGIM 314 Query: 309 AGAAPAPATLKAMQEIGGYMCH-----VYGLTETYGPHSICEWRREWDSLPLEEQAKLKA 363 AG+ P + M+++ M YGLTE + R D + ++ +A Sbjct: 315 AGS---PCPVNVMKKVIDKMSMKDITICYGLTEA---SPVMTQTRMEDDIKRRTESVGRA 368 Query: 364 RQGIPYVSFEMDVFDANGKPVPWDGKTIGEVVMRGHNVALGYYKNPEKTAESFR-DGWFH 422 I F + GK + G+T GE+ RG+NV GYY NPE T+ + DGW H Sbjct: 369 MPEIEVAIFNPET----GKECSY-GET-GEICCRGYNVMEGYYNNPEATSTAIDIDGWLH 422 Query: 423 SGDAAVVHPDGYIEIVDRFKDLINTGGEKVSSILVEKTLMEIPGVKAVAVYGTPDEKWGE 482 SGD + +GY+ + R KD+I GGE + +E+ L + G+ V V G P +K+GE Sbjct: 423 SGDLGTMDEEGYVVVTGRLKDMIIRGGENIYPREIEEFLYGMEGILDVQVAGVPSKKFGE 482 Query: 483 VVTARIELQEGVKLTEEEVIKFCKERLAHFECPKIVEF-GPIPMTATGKMQKYVLRNEA 540 V A I L++ V++ +++VI +C+ ++A ++ PK + F PMTA+GK+QK+ LR+ A Sbjct: 483 QVGAFIILKDDVEIDKQDVIDYCRGKIARYKIPKFITFIDAYPMTASGKIQKFKLRDMA 541 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: 709 Number of extensions: 36 Number of successful extensions: 5 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: 548 Length adjustment: 36 Effective length of query: 513 Effective length of database: 512 Effective search space: 262656 Effective search space used: 262656 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