Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate WP_073036227.1 BUB04_RS01345 dihydrolipoamide acetyltransferase family protein
Query= reanno::Smeli:SMc03203 (426 letters) >NCBI__GCF_900129305.1:WP_073036227.1 Length = 430 Score = 241 bits (615), Expect = 3e-68 Identities = 161/446 (36%), Positives = 233/446 (52%), Gaps = 51/446 (11%) Query: 7 KMPDVGEGVAEAELVEWHVKPGDPVREDMVLAAVMTDKATVEIPSPVTGKVLWLGAEVGD 66 ++PD+GEG+ E E+++ V G+ V E V+ V TDKA VEIPSP TG V + + G Sbjct: 6 RLPDLGEGIHEGEIIDVLVSVGETVTEGQVILIVETDKAAVEIPSPFTGVVEAVHVKAGQ 65 Query: 67 TVAVKAPLVRIETAGEAGEAAPDSIPEALAEQVLDEPVAVSSRLEAKAP-PQPEKPAPKP 125 V V PL+ + E EA P+ R EA AP P PEK A K Sbjct: 66 VVHVGDPLLAVAGEEEEREAKPER------------------RAEATAPEPAPEK-AEKE 106 Query: 126 APAPREAPDLSAKPLASPAVRLRARESGIDLRQVAGTGPAGRITHEDLDLFISRGA---- 181 PREA ASP+ R AR+ G+DLR V GTGP GR+T ED+ R Sbjct: 107 EGVPREA---ELPVAASPSTRKLARQLGVDLRAVKGTGPEGRVTAEDVRRAADRAKAPAA 163 Query: 182 --------EPLPAQ-------TGLVRKTAVEEVR----MIGLRRRIAEKMSLSTSRIPHI 222 EP PA+ G R+ EVR + +RR IA +M+LS +IPH+ Sbjct: 164 PVEPSAAREPSPAEREGVEPGAGAARELRPSEVRERVPLKSVRRSIARRMALSW-KIPHV 222 Query: 223 TYVEEVDMTALEDLRATMNRDRKPEQAKLTILPFLMRALVKTVAEQPGVNATFDDHAGVI 282 ++ + D+T LE LR + E LT+ FL++A + + P NA+ D+ A I Sbjct: 223 SHHDLADITDLERLRREVLESPALEGVHLTLTAFLVKAAGAALRKFPSFNASLDEEAEEI 282 Query: 283 HRHAAVHIGIATQTPAGLTVPVVRHAEARGIWDCAAELNRLADAARTGTATRDELTGSTI 342 + ++H+G+A TP GL VPV+R E + + + A EL L A+ + ++ T Sbjct: 283 LIYRSIHVGVAMDTPRGLVVPVIRDVEGKSLREVAEELEELGGKAQEARLSPADIRDGTF 342 Query: 343 TISSLGAIGGIASTPVINHPEVAIVGVNKIAVRPVWDGA----QFVPRKIMNLSSSFDHR 398 T++++G++GG TP+I+ P+VAI+G + ++ PV G + R ++ L +FDHR Sbjct: 343 TVTNIGSLGGRGFTPLIHPPQVAILGAGRASLEPVVKGTLEDHRMEVRLMLPLVLAFDHR 402 Query: 399 VIDGWDAAVFVQRLKTLLETPALIFV 424 V+DG D A F+ LK LLE P L+ V Sbjct: 403 VVDGADGARFLNHLKALLEDPKLLLV 428 Lambda K H 0.317 0.133 0.384 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: 469 Number of extensions: 25 Number of successful extensions: 5 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: 426 Length of database: 430 Length adjustment: 32 Effective length of query: 394 Effective length of database: 398 Effective search space: 156812 Effective search space used: 156812 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: 51 (24.3 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