Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_011383120.1 AMB_RS03480 isovaleryl-CoA dehydrogenase
Query= reanno::Smeli:SM_b21121 (387 letters) >NCBI__GCF_000009985.1:WP_011383120.1 Length = 389 Score = 617 bits (1591), Expect = 0.0 Identities = 309/386 (80%), Positives = 331/386 (85%) Query: 2 FEAGLNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITAD 61 F + LNF LGE D +R SV FA+ IAP A + DRSN FP LW +G +GLLGIT D Sbjct: 4 FNSALNFDLGETADMMRDSVAAFAATEIAPRAAEIDRSNEFPNELWPRLGAMGLLGITVD 63 Query: 62 EAHGGAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLIS 121 E +GGAG+GYL H VAMEEISRASASVGLSYGAHSNLCVNQI RNG AQK +YLPKLIS Sbjct: 64 EKYGGAGMGYLEHVVAMEEISRASASVGLSYGAHSNLCVNQIKRNGTEAQKMKYLPKLIS 123 Query: 122 GEHVGALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAA 181 GE++GALAMSEP AGSDVVSMKLKA+K+GDRYVLNG+KMWITNGPDADV+VVYAKTD A Sbjct: 124 GEYIGALAMSEPNAGSDVVSMKLKAEKKGDRYVLNGTKMWITNGPDADVIVVYAKTDVTA 183 Query: 182 GPRGITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLM 241 GPRGITAFLVEK F GFS QKLDKLGMRGSNT EL+F DCEVPEENVLG VG+GV VLM Sbjct: 184 GPRGITAFLVEKTFKGFSVAQKLDKLGMRGSNTGELVFQDCEVPEENVLGAVGKGVNVLM 243 Query: 242 SGLDYERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAAR 301 SGLDYERVVL+ GPLGIMAAC+DVVVPY+HER QFGQPIG FQLMQGKLADMY T NA R Sbjct: 244 SGLDYERVVLTGGPLGIMAACMDVVVPYVHERTQFGQPIGTFQLMQGKLADMYTTFNACR 303 Query: 302 AYVYAVAAACDRGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDA 361 AY YAVA ACDRGET+RKDAAG ILY AEKAT MALEAIQ LGGNGY N+Y GRLLRDA Sbjct: 304 AYTYAVAKACDRGETSRKDAAGVILYGAEKATWMALEAIQTLGGNGYINEYATGRLLRDA 363 Query: 362 KLYEIGAGTSEIRRMLIGRELFAETK 387 KLYEIGAGTSEIRRMLIGRELF ETK Sbjct: 364 KLYEIGAGTSEIRRMLIGRELFEETK 389 Lambda K H 0.318 0.135 0.391 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: 475 Number of extensions: 11 Number of successful extensions: 1 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: 387 Length of database: 389 Length adjustment: 30 Effective length of query: 357 Effective length of database: 359 Effective search space: 128163 Effective search space used: 128163 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 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