Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate WP_035135277.1 Q763_RS13690 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_3542 (425 letters) >NCBI__GCF_000769915.1:WP_035135277.1 Length = 408 Score = 226 bits (577), Expect = 8e-64 Identities = 143/422 (33%), Positives = 228/422 (54%), Gaps = 29/422 (6%) Query: 6 IKMPDIGEGIAEVELSVWHVKVGDMVVEDQVLADVMTDKAMVDIPSPVHGKVIALGGQPG 65 +K+P GE I EVE++ W V GD V +DQ +A+V +DKA +++P+ G +I L + G Sbjct: 5 MKVPSPGESITEVEIATWLVSDGDYVEKDQAIAEVDSDKATLELPAEASG-IITLKAEEG 63 Query: 66 EVMAVGSVLISIEVEGAGNVKESAQPAPVVKEAPVAATKVETVVESKPVAAPAPKAAVCQ 125 + +AVG V+ I+ GA + SA P +E A K E E APA K Sbjct: 64 DAVAVGQVVCLIDT-GAAKPEGSA---PAKEEKKEEAPKAEEKKEEPKKEAPAEKTYATG 119 Query: 126 GPMVAREADERPLASPAVRKHALDLGIQLRLVRGTGPAGRVLHEDLDAYLAQGQSNASAP 185 P SPA RK + I V GTG GRV +D NA A Sbjct: 120 TP------------SPAARKILDEKNIDPATVTGTGKGGRVTKDDA--------VNAKAS 159 Query: 186 VAAAYAQRTDEQQIPVIGMRRKIAQRMQDATQRAAHFSYVEEIDVTAVEELRAHLNEKHG 245 + ++ + +RRK+A+R+ A A + E+++T + ++RA ++ Sbjct: 160 MGTPTGGNRASERTKLSMLRRKVAERLVSAKNETAMLTTFNEVNMTPINKVRAEFKDEFK 219 Query: 246 ATRGKLTL--LPFLVRALVVALRDFPQINARYDDEAQVITRLGAVHVGIATQADIGLMVP 303 A G ++L + F +A+V AL+ +P +N+ D + +V V V IA GLMVP Sbjct: 220 AKHGGVSLGFMSFFTKAVVRALQLYPDVNSMMDGDYKV--SYDFVDVSIAVSGPKGLMVP 277 Query: 304 VVRHAEARSLWDSAAEISRLATAARNGKASRDELSGSTITLTSLGALGGIVSTPVLNLPE 363 VVR+AEA + AEI RLA AR+G+ + D+++G T T+T+ G G ++STP++N P+ Sbjct: 278 VVRNAEALTFRGIEAEIKRLALRARDGQITVDDMTGGTFTITNGGVFGSMLSTPIINPPQ 337 Query: 364 VAIVGVNKIVERPMVIKGQIVIRKMMNLSSSFDHRVVDGMDAALFIQAIRGLLEQPATLF 423 I+G++ I+ERP+ + G++ I MM ++ S+DHR++DG ++ F+ A++ LE P L Sbjct: 338 SGILGMHNIIERPIAVDGKVEIHPMMYVALSYDHRIIDGRESVGFLVAVKEGLENPVELL 397 Query: 424 VE 425 ++ Sbjct: 398 MD 399 Lambda K H 0.318 0.133 0.368 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: 347 Number of extensions: 16 Number of successful extensions: 4 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: 425 Length of database: 408 Length adjustment: 31 Effective length of query: 394 Effective length of database: 377 Effective search space: 148538 Effective search space used: 148538 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 24 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:
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