Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate WP_011951627.1 SWIT_RS03975 2-oxo acid dehydrogenase subunit E2
Query= reanno::pseudo6_N2E2:Pf6N2E2_479 (423 letters) >NCBI__GCF_000016765.1:WP_011951627.1 Length = 421 Score = 435 bits (1119), Expect = e-126 Identities = 226/427 (52%), Positives = 295/427 (69%), Gaps = 10/427 (2%) Query: 1 MGTHVIKMPDIGEGIAEVELSVWHVKVGDMVVEDQVLADVMTDKAMVDIPSPVHGRVIAL 60 MG ++ +MPD+GEG+AE E+ WHVK GD + EDQ L DVMTDKA VD+ SPV G V+AL Sbjct: 1 MGRYLFRMPDVGEGVAEAEIIAWHVKPGDSIAEDQSLVDVMTDKATVDMTSPVAGTVVAL 60 Query: 61 GGEPGEVMAVGSELIRIEVEGAGNLKESAQ----QAPTPTPAAQAPKPAPVATPEPVLEK 116 GE GE+ AVGS L+ +EVEG GN ++ +A P A AP P +A P+ V Sbjct: 61 HGEIGELRAVGSTLVELEVEGEGNGADAPAVVVVEAAAPVVEA-APAPPVIAAPKAVQPP 119 Query: 117 TAAPRCAPQAPVARDPDERPLASPAVRKHALDLGIQLRLVQGSGPAGRVLHEDLEAYLAQ 176 +A P A R P + PLA+PA R+ A +LGI L+ V G+GP GR+ EDL+ Y+ Sbjct: 120 SAQPAFA-----TRTPGQEPLAAPATRRRAHELGIALQYVPGTGPGGRITSEDLDRYVET 174 Query: 177 GPSVQAKGGSGYAERHDEQQIPVIGMRRKIAQRMQEATQRAAHFSYVEEIDITALEELRV 236 G ++ A G R + ++GMRRKIA++MQEA +R H +YVEE D+T LE LR Sbjct: 175 GGALAAGGAGRLTPRTGGSDVRIVGMRRKIAEKMQEAKRRIPHITYVEECDLTELEALRA 234 Query: 237 HLNEKHGASRGKLTLLPFLVRALVVALRDFPQMNARYDDEAQVIHRSGAVHVGVATQSDV 296 LN + KLTLLPF +RAL L FPQ+NARYDD+A V+H+S A+H+G+ATQ+ Sbjct: 235 DLNAHREEGQPKLTLLPFFIRALARVLPRFPQVNARYDDDAGVLHQSDAIHLGIATQTPA 294 Query: 297 GLMVPVVRHAEARSLWDNAAEISRLATAARTGKASRDELSGSTITLTSLGALGGIVSTPV 356 GL+VPV+RHAEA L A EI+RL+ AAR G A+R+E+SG+TIT+TSLG LGG+ STP+ Sbjct: 295 GLLVPVIRHAEALDLRALAEEIARLSKAARDGSATREEMSGATITITSLGTLGGVTSTPI 354 Query: 357 LNLPEVAIVGVNKIVERPVVIKGQIVIRKMMNLSSSFDHRVVDGMDAAQFIQALRGLLEQ 416 +N PEVAI+G NK+VERP V + +RKMMNLSSSFDHR+VDG DAA F+Q L+ LLE Sbjct: 355 VNHPEVAIIGPNKLVERPTVQGSFVTVRKMMNLSSSFDHRIVDGYDAALFVQQLKRLLEH 414 Query: 417 PATLFVE 423 PA +F++ Sbjct: 415 PALIFMD 421 Lambda K H 0.317 0.133 0.375 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: 544 Number of extensions: 20 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: 423 Length of database: 421 Length adjustment: 32 Effective length of query: 391 Effective length of database: 389 Effective search space: 152099 Effective search space used: 152099 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 (21.6 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