Align 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (EC 1.2.4.4) (characterized)
to candidate GFF61 HP15_61 chain A, alpha-keto acid dehydrogenase-like protein
Query= reanno::pseudo3_N2E3:AO353_26635 (411 letters) >FitnessBrowser__Marino:GFF61 Length = 409 Score = 488 bits (1257), Expect = e-142 Identities = 239/406 (58%), Positives = 300/406 (73%), Gaps = 1/406 (0%) Query: 6 EPLRLHVPEPSGRPGCKTDFSYLRLTDAGTVRKPPIDVEPADTADLAKGLIRVLDDQGNA 65 +PL LHVPEP RPG K FS+L + +AG RKP + +D DL GL+RVLDD G A Sbjct: 5 KPLHLHVPEPPARPGDKPSFSHLVIPEAGETRKPDVTDSESDMRDLPYGLVRVLDDNGAA 64 Query: 66 LGPWAEGVPVEILRKGMRAMLKTRIFDNRMVVAQRQKKMSFYMQSLGEEAIGSAQALALN 125 +GPW G+ ++LRKG+R+ML TR+FD R+ RQ K SFYM+S GEEAIG+AQ+LAL+ Sbjct: 65 IGPWDPGLSPDVLRKGLRSMLLTRVFDERLFRVHRQGKTSFYMKSTGEEAIGAAQSLALS 124 Query: 126 IDDMCFPTYRQQSILMAREVPLVDLICQLLSNERDPLKGRQLPIMYSVKDAGFFTISGNL 185 DMCFPTYR S LMAR+ PL+D++ Q+ SNE+DPLKGRQLPI++S +D GF+++SGN+ Sbjct: 125 QGDMCFPTYRVMSWLMARDYPLIDMVNQIFSNEKDPLKGRQLPILFSARDYGFYSLSGNV 184 Query: 186 ATQFVQGVGWGMASAIKGDTKIASAWIGDGATAESDFHTALTFAHVYRAPVILNVVNNQW 245 ++F VGW MASA KGD KIA +IG+G TAE DFH ALTFA VYRAPVIL V NNQW Sbjct: 185 GSRFGHAVGWAMASAYKGDDKIALGYIGEGTTAEGDFHEALTFASVYRAPVILCVTNNQW 244 Query: 246 AISTFQAIAGGEATTFAGRGVGCGIASLRVDGNDFVAVYAASAWAAERARRNLGPTMIEW 305 AIS++ IAG EATTFA + + G+ LRVDGNDF+AV++A+ WAAERAR NLG T+IE+ Sbjct: 245 AISSYSGIAGAEATTFAAKALAYGLPGLRVDGNDFLAVWSATKWAAERARNNLGATLIEF 304 Query: 306 VTYRAGPHSTSDDPSKYRPADDWSHFPLGDPIARLKQHLVKIGQWSEEEHVALSAELEAE 365 TYRA HSTSDDP+KYRPAD+ H+PLGDP+ RLK HL+ +G+W +E H AL+ EL Sbjct: 305 FTYRAAGHSTSDDPTKYRPADEAEHWPLGDPLERLKHHLISLGEWDDERHEALTDELSET 364 Query: 366 IIAAQKEAEQYGTLAGGQIPSAATMFEDVYKEMPEHLKRQRQELGI 411 + AA KE E GTL G PS MFE V+ E + QR+E+GI Sbjct: 365 VRAAVKEGEAVGTL-GQSKPSVREMFEGVFAEPDWRVLEQRREVGI 409 Lambda K H 0.319 0.134 0.403 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: 512 Number of extensions: 16 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: 411 Length of database: 409 Length adjustment: 31 Effective length of query: 380 Effective length of database: 378 Effective search space: 143640 Effective search space used: 143640 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