Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate WP_011427699.1 RHE_RS23210 dihydrolipoamide acetyltransferase family protein
Query= reanno::Smeli:SMc03203 (426 letters) >NCBI__GCF_000092045.1:WP_011427699.1 Length = 413 Score = 609 bits (1571), Expect = e-179 Identities = 313/426 (73%), Positives = 355/426 (83%), Gaps = 13/426 (3%) Query: 1 MGEFIIKMPDVGEGVAEAELVEWHVKPGDPVREDMVLAAVMTDKATVEIPSPVTGKVLWL 60 MGEFIIKMPDVGEGVAEAELVEWHVK GDPVREDMV+AAVMTDKATVEIPSPV G V+WL Sbjct: 1 MGEFIIKMPDVGEGVAEAELVEWHVKTGDPVREDMVIAAVMTDKATVEIPSPVNGTVIWL 60 Query: 61 GAEVGDTVAVKAPLVRIETAGEAGEAAPDSIPEALAEQVLDEPVAVSSRLEAKAPPQPEK 120 EVGD +AVKAPLVRIET G AGEA P I +A +V V + + AP P Sbjct: 61 AGEVGDRIAVKAPLVRIETGG-AGEAQPMRISQAPTAEV------VKAEIARPAPTAPVS 113 Query: 121 PAPKPAPAPREAPDLSAKPLASPAVRLRARESGIDLRQVAGTGPAGRITHEDLDLFISRG 180 AP A P E KPLA+P+VRL ARESG+DLRQV G+GPAGRI ED++ F+ +G Sbjct: 114 AAPAAAAPPVE------KPLAAPSVRLFARESGVDLRQVQGSGPAGRILREDVEQFLVQG 167 Query: 181 AEPLPAQTGLVRKTAVEEVRMIGLRRRIAEKMSLSTSRIPHITYVEEVDMTALEDLRATM 240 A P+ + G V+KTA EEV++ GLRRRIAEKM LSTSRIPHITYVEEVD+TALE+LRATM Sbjct: 168 AAPVLVKGGSVKKTATEEVKLTGLRRRIAEKMVLSTSRIPHITYVEEVDVTALEELRATM 227 Query: 241 NRDRKPEQAKLTILPFLMRALVKTVAEQPGVNATFDDHAGVIHRHAAVHIGIATQTPAGL 300 N DR+ KLT+LPFL+RALVK ++EQP VNATFDD AG+I RH+AVHIGIATQTPAGL Sbjct: 228 NGDRREGHPKLTVLPFLLRALVKAISEQPEVNATFDDDAGIITRHSAVHIGIATQTPAGL 287 Query: 301 TVPVVRHAEARGIWDCAAELNRLADAARTGTATRDELTGSTITISSLGAIGGIASTPVIN 360 TVPVVRHAEARGIWDCA+E+ RLA+AAR+GTATRDEL+GSTITISSLG +GGI STPVIN Sbjct: 288 TVPVVRHAEARGIWDCASEVVRLAEAARSGTATRDELSGSTITISSLGPLGGIVSTPVIN 347 Query: 361 HPEVAIVGVNKIAVRPVWDGAQFVPRKIMNLSSSFDHRVIDGWDAAVFVQRLKTLLETPA 420 HPEVAI+GVNKIA RP+WDG QFVPRK+MNLSSSFDHR+IDGWDAA FVQR++TLLETPA Sbjct: 348 HPEVAIIGVNKIATRPIWDGTQFVPRKMMNLSSSFDHRIIDGWDAATFVQRIRTLLETPA 407 Query: 421 LIFVEG 426 LIF+EG Sbjct: 408 LIFIEG 413 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: 587 Number of extensions: 14 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: 426 Length of database: 413 Length adjustment: 32 Effective length of query: 394 Effective length of database: 381 Effective search space: 150114 Effective search space used: 150114 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