Align 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (EC 1.2.4.4) (characterized)
to candidate WP_011427697.1 RHE_RS23200 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) subunit alpha
Query= reanno::Smeli:SMc03201 (410 letters) >NCBI__GCF_000092045.1:WP_011427697.1 Length = 410 Score = 756 bits (1953), Expect = 0.0 Identities = 373/410 (90%), Positives = 391/410 (95%) Query: 1 MDEFSRLSLHVPEPAVRPGDLPDFSNVKIPKAGSVPRPDVDVDPEEIRDLAYSIIRVLNR 60 M + + LSLHVPEPAVRPG PDFSNVKI KAGSVPRP+VDV E+IRDLAYSIIRVLNR Sbjct: 1 MVDSAHLSLHVPEPAVRPGGQPDFSNVKIAKAGSVPRPEVDVASEDIRDLAYSIIRVLNR 60 Query: 61 EGEAVGPWAGFLSDEELLTGLRHMMLLRAFDARMLMAQRQGKTSFYMQHLGEEAVSCAFR 120 +GEAVGPWAG L+DEELLTGLR+MM LRAFDARMLMAQRQGKTSFYMQHLGEEAVSCAFR Sbjct: 61 DGEAVGPWAGSLNDEELLTGLRNMMKLRAFDARMLMAQRQGKTSFYMQHLGEEAVSCAFR 120 Query: 121 KALRKGDMNFPTYRQAGLLIADDYPMVEMMNQIFSNELDPCHGRQLPVMYTSKEHGFFTI 180 KAL KGDMNFPTYRQAGLLIADDYPMVEMMNQI+SNE DP HGRQLP+MY+SKEHGFFTI Sbjct: 121 KALAKGDMNFPTYRQAGLLIADDYPMVEMMNQIYSNESDPLHGRQLPIMYSSKEHGFFTI 180 Query: 181 SGNLATQYVQAVGWAMASAIKNDTRIAAGWIGDGSTAESDFHSALVFASTYKAPVILNIV 240 SGNLATQYVQAVGWAMASAIKND+RIAA WIGDGSTAESDFHSALVFASTYKAPVILNIV Sbjct: 181 SGNLATQYVQAVGWAMASAIKNDSRIAAAWIGDGSTAESDFHSALVFASTYKAPVILNIV 240 Query: 241 NNQWAISTFQGIARGGSGTFAARGLGFGIPALRVDGNDYLAVYAVARWAAERARLNLGPT 300 NNQWAISTFQGIARGGSGTFAARGLGFGIPALRVDGNDYLAV+AVARWAAERAR NLGPT Sbjct: 241 NNQWAISTFQGIARGGSGTFAARGLGFGIPALRVDGNDYLAVHAVARWAAERARRNLGPT 300 Query: 301 LIEYVTYRVGAHSTSDDPSAYRPKTESEAWPLGDPVLRLKKHLILRGAWSEERHAQAEAE 360 LIE+VTYRVGAHSTSDDPSAYRPKTESEAWPLGDPVLRLKKHLI++G WSEERH QAEAE Sbjct: 301 LIEHVTYRVGAHSTSDDPSAYRPKTESEAWPLGDPVLRLKKHLIVKGVWSEERHVQAEAE 360 Query: 361 IMDEVIQAQKEAERHGTLHAGGRPSVRDIFEGVYAEMPPHIRRQRQKAGY 410 IMDEVI+AQ++AE HGTLHAGGRPSVRDIFEGVYAEMP HIRRQRQKAGY Sbjct: 361 IMDEVIEAQRQAEAHGTLHAGGRPSVRDIFEGVYAEMPAHIRRQRQKAGY 410 Lambda K H 0.320 0.135 0.410 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: 736 Number of extensions: 26 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: 410 Length of database: 410 Length adjustment: 31 Effective length of query: 379 Effective length of database: 379 Effective search space: 143641 Effective search space used: 143641 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 Apr 09 2024. 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:
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