Align 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (EC 1.2.4.4) (characterized)
to candidate GFF1731 PGA1_c17550 pyruvate dehydrogenase E1 component subunit alpha
Query= BRENDA::Q72GU1 (367 letters) >FitnessBrowser__Phaeo:GFF1731 Length = 337 Score = 149 bits (377), Expect = 8e-41 Identities = 103/322 (31%), Positives = 159/322 (49%), Gaps = 4/322 (1%) Query: 32 DLEGEKLRRLYRDMLAARMLDERYTILIRTGKTS-FIAPAAGHEAAQVAIAHAIRPGFDW 90 ++ ++L YR+ML R +E+ L G F G EA V + A G D Sbjct: 11 NVSADELLEYYREMLLIRRFEEKAGQLYGMGLIGGFCHLYIGQEAVVVGLEAAAEDG-DK 69 Query: 91 VFPYYRDHGLALALGIPLKELFGQMLATKADPNKGRQMPEHPGSKALNFFTVASPIASHV 150 YRDHG LA G+ + ++ + +KG+ H SK +F+ + + V Sbjct: 70 RVTSYRDHGHMLACGMDPSGVMAELTGREGGYSKGKGGSMHMFSKEKHFYGGHGIVGAQV 129 Query: 151 PPAAGAAISMKLLRTGQVAVCTFGDGATSEGDWYAGINFAAVQGAPAVFVCENNFYAISV 210 P AG A S K +V FGDGA ++G Y N A + P VFV ENN YA+ Sbjct: 130 PLGAGLAFSDKYKGNDRVTFAYFGDGAANQGQVYETYNMAQLWDLPVVFVIENNQYAMGT 189 Query: 211 DYRHQTHSPTIADKAHAFGIPGYLVDGMDVLASYYVVKEAVERARRGEGPSLVELRVYRY 270 + T SP + + A+GI G VDGMDVLA + AV R G+GP ++E++ YRY Sbjct: 190 SVQRSTKSPALWKRGEAYGIKGEEVDGMDVLAVKEAGERAVAHCRAGKGPYILEVKTYRY 249 Query: 271 GPHSSADDDSRYRPKEEVAFWR-KKDPIPRFRRFLEARGLWNEEWEEDVREEIRAELERG 329 HS + D ++YR +EEV R ++DPI + R L E+ + + +EI+ + + Sbjct: 250 RGHSMS-DPAKYRTREEVQKMREERDPIEQVRDMLLTGKHATEDDLKAIDKEIKDIVNKS 308 Query: 330 LKEAEEAGPVPPEWMFADVFAE 351 ++E+ E ++ D++A+ Sbjct: 309 ADFSKESPEPALEELWTDIYAD 330 Lambda K H 0.320 0.138 0.426 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: 346 Number of extensions: 25 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: 367 Length of database: 337 Length adjustment: 29 Effective length of query: 338 Effective length of database: 308 Effective search space: 104104 Effective search space used: 104104 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: 49 (23.5 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