Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate GFF2 HP15_2 acyl-CoA dehydrogenase domain protein
Query= reanno::SB2B:6937192 (389 letters) >lcl|FitnessBrowser__Marino:GFF2 HP15_2 acyl-CoA dehydrogenase domain protein Length = 389 Score = 616 bits (1589), Expect = 0.0 Identities = 302/386 (78%), Positives = 341/386 (88%), Gaps = 1/386 (0%) Query: 1 MSHLYSTLNFGLGEDVDMLRDAVYEFAKGEIAPLAEKVDRDNAFPNELWAKFGDMGLLGV 60 M YS LNFGLGE +DMLR+ + FA EIAP AE++DR+N FP +LW K GDMGLLG+ Sbjct: 1 MKSQYSELNFGLGETLDMLREQINGFAASEIAPRAEEIDRNNEFPMDLWRKMGDMGLLGI 60 Query: 61 TVAEEYGGVNMGYLAHVVAMEEISRASASIGLSYGAHSNLCVNQIYRNGNEAQRAKYLPK 120 TV+EEYGG +MGYLAHV+AMEEISRASAS+GLSYGAHSNLCVNQI+RNG E Q+ KYLPK Sbjct: 61 TVSEEYGGSDMGYLAHVIAMEEISRASASVGLSYGAHSNLCVNQIHRNGTEEQKQKYLPK 120 Query: 121 LISGEHIGALAMSEPNAGSDVVSMKLHARKEGDRYILNGNKMWITNGPDAHTYVIYAKTD 180 L+SGEHIGALAMSEPNAGSDV+SMKL A+ EGD Y+LNGNKMWITNGPDA+TYVIYAKTD Sbjct: 121 LVSGEHIGALAMSEPNAGSDVISMKLTAKDEGDHYLLNGNKMWITNGPDANTYVIYAKTD 180 Query: 181 LDKGPHGITAFIVERGFKGFSQAQKLDKLGMRGSNTCELVFEDCEVPEENILGGLNNGVK 240 G G+TAFIVER GFS+ QKLDKLGMRGSNTCELVF+DC+VP+EN+LGG+ NG K Sbjct: 181 TSAGSRGVTAFIVERDAPGFSRHQKLDKLGMRGSNTCELVFQDCKVPKENVLGGVGNGAK 240 Query: 241 VLMSGLDYERVVLSGGPLGIMTACMDIVVPYVHERVQFGKSIGEFQLVQGKLADMYTGMN 300 VLMSGLDYER+VLSGGPLGIM A MD+VVPY+ ER QFG++IGEF+LVQGK+ADMYT MN Sbjct: 241 VLMSGLDYERLVLSGGPLGIMQAAMDVVVPYIRERKQFGQAIGEFELVQGKVADMYTWMN 300 Query: 301 AAKSYVYNVARACDRG-ETTRKDAAGVILYAAELATKMALDAIQLLGGNGYVNEYATGRL 359 AKSYVY VA + DRG ETTRKDAAG ILY+AE+ATK+ALDAIQLLGGNGY+NEY TGRL Sbjct: 301 TAKSYVYMVAMSADRGAETTRKDAAGAILYSAEMATKIALDAIQLLGGNGYINEYPTGRL 360 Query: 360 LRDAKLYEIGAGTSEIRRMLIGRELF 385 LRDAKLYEIGAGTSEIRRMLIGREL+ Sbjct: 361 LRDAKLYEIGAGTSEIRRMLIGRELY 386 Lambda K H 0.318 0.137 0.396 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: 575 Number of extensions: 14 Number of successful extensions: 2 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: 389 Length of database: 389 Length adjustment: 30 Effective length of query: 359 Effective length of database: 359 Effective search space: 128881 Effective search space used: 128881 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 preprint 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