Align 3-hydroxybutyryl-CoA dehydrogenase; EC 1.1.1.35 (characterized)
to candidate BPHYT_RS06760 BPHYT_RS06760 3-hydroxyacyl-CoA dehydrogenase
Query= SwissProt::Q0AVM2 (279 letters) >FitnessBrowser__BFirm:BPHYT_RS06760 Length = 521 Score = 216 bits (551), Expect = 6e-61 Identities = 112/278 (40%), Positives = 166/278 (59%), Gaps = 1/278 (0%) Query: 3 IMVLGAGTMGAGIVQTAAQAGFEVVVRDIKQEFVDRGIAGIDKLLSKNVDKGRMTAEDKA 62 I ++G G MG GI Q AA AG V + D + + + +K KG++ Sbjct: 11 IGIVGTGAMGRGIAQIAALAGLTVRLYDTNPAAIGAARDYLAETFAKLTAKGKLDQARSL 70 Query: 63 AVMGRISGTVDMGAAADCDLVIEAALEVMDIKKAIFKELDSICKPECILASNTSALSVTE 122 A + +SG +G A CDLV+EA +E +D+K+A+F+EL+++ C+LASNTS+LS+T Sbjct: 71 AALANVSGAQSIGELAGCDLVVEAIVEKLDVKQALFRELETVVSGRCVLASNTSSLSITA 130 Query: 123 IAAATGRADKVIGMHFFNPVPAMKLVEVIRGASTSQATYDAIKDLSVKMGKSPVEINEAP 182 IAA +V+G HFFNPVP MK+VEVI G + A DA+ +L+ +MG +PV + P Sbjct: 131 IAAGCSDPSRVVGYHFFNPVPLMKVVEVIDGLRSDPAAGDALMNLARRMGHTPVRAKDMP 190 Query: 183 GFVVNRLLIPMLNEGMYCLMEGVANAADIDTSMKFGAGHPMGPLALADMIGLDICLKIME 242 GF+VN M EG+ EGVA+ ADID ++ AG +GP L D+ LD+ +ME Sbjct: 191 GFIVNHAGRGMNTEGLRVAGEGVASFADIDRIVREQAGFRLGPFELLDLTALDVSHPVME 250 Query: 243 TLYKEF-GDPKYRPCPLLAKMVRANKLGRKTGEGFFAY 279 ++Y +F +P++ P P+ + +GRKTGEGF+ Y Sbjct: 251 SIYHQFYEEPRFTPSPITGTRLAGGLIGRKTGEGFYRY 288 Score = 72.4 bits (176), Expect = 2e-17 Identities = 38/132 (28%), Positives = 65/132 (49%) Query: 130 ADKVIGMHFFNPVPAMKLVEVIRGASTSQATYDAIKDLSVKMGKSPVEINEAPGFVVNRL 189 A +V+ + P+ + ++ +T++ D L G I ++ GFV R+ Sbjct: 365 ATRVVAIDALFPLVGAQRRTLMTTPATTRTARDTAHALFAADGVPVTVIRDSTGFVAQRV 424 Query: 190 LIPMLNEGMYCLMEGVANAADIDTSMKFGAGHPMGPLALADMIGLDICLKIMETLYKEFG 249 + ++N G + +A DID ++ G G+P GPL L D +G L I+ ++ G Sbjct: 425 VATIVNIGCDIAQKQIATPQDIDLAVTLGLGYPRGPLGLGDALGSTTILTILRNMFSVLG 484 Query: 250 DPKYRPCPLLAK 261 DP+YRP P LA+ Sbjct: 485 DPRYRPSPWLAR 496 Lambda K H 0.321 0.137 0.389 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: 376 Number of extensions: 20 Number of successful extensions: 3 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: 279 Length of database: 521 Length adjustment: 30 Effective length of query: 249 Effective length of database: 491 Effective search space: 122259 Effective search space used: 122259 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 (21.8 bits) S2: 50 (23.9 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