Align Enoyl-CoA hydratase [valine degradation] (EC 4.2.1.17) (characterized)
to candidate BWI76_RS20065 BWI76_RS20065 1,4-dihydroxy-2-naphthoyl-CoA synthase
Query= reanno::psRCH2:GFF2389 (257 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS20065 BWI76_RS20065 1,4-dihydroxy-2-naphthoyl-CoA synthase Length = 285 Score = 127 bits (320), Expect = 2e-34 Identities = 93/252 (36%), Positives = 130/252 (51%), Gaps = 16/252 (6%) Query: 14 VALITLNRPQALNALNGQLISELNQALGQLEADPQIGCIVLTGSA-KAFAAGADIKEMAE 72 +A IT+NRPQ NA + E+ QAL D IG IVLTG KAF AG D K + Sbjct: 34 IAKITINRPQVRNAFRPLTVKEMIQALADARYDDNIGVIVLTGEGDKAFCAGGDQKVRGD 93 Query: 73 LTYPQIYLDDF------FADADR-IATRRKPLIAAVAGYALGGGCELALLCDMIFAADNA 125 Y DD D R I T KP++A VAGY++GGG L ++CD+ AA+NA Sbjct: 94 YGG---YQDDSGVHHLNVLDFQRQIRTCPKPVLAMVAGYSIGGGHVLHMMCDLTIAAENA 150 Query: 126 RFGQPEVNLGVLPGIGGTQRLTRAVGKAKAMDMCLTGRQMDAAEAERAGLVARVFPAESL 185 FGQ +G G G + R VG+ KA ++ RQ DA +A GLV V P L Sbjct: 151 IFGQTGPKVGSFDGGWGASYMARIVGQKKAREIWFLCRQYDAQQALDMGLVNTVVPLADL 210 Query: 186 LEETLKAARVIAEKSLPATMMIKESVNRAF--ETTLAEGIRFERRVFHAVFATADQKEGM 243 +ET++ R + + S A +K ++N + L E +F + T + +EG Sbjct: 211 EKETVRWCREMLQNSPMALRCLKAALNADCDGQAGLQELAGNATMLF---YMTEEGQEGR 267 Query: 244 AAFSEKRKPEFT 255 AF++KR+P+F+ Sbjct: 268 NAFNQKRQPDFS 279 Lambda K H 0.321 0.135 0.375 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: 147 Number of extensions: 11 Number of successful extensions: 3 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: 257 Length of database: 285 Length adjustment: 25 Effective length of query: 232 Effective length of database: 260 Effective search space: 60320 Effective search space used: 60320 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 (21.9 bits) S2: 47 (22.7 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