Align D-lactate dehydrogenase (EC 1.1.1.28); D-lactate dehydrogenase (acceptor) (EC 1.1.99.6) (characterized)
to candidate WP_017557059.1 C892_RS0109975 FAD-binding protein
Query= BRENDA::Q9YEU4 (473 letters) >NCBI__GCF_000341205.1:WP_017557059.1 Length = 483 Score = 204 bits (519), Expect = 5e-57 Identities = 149/475 (31%), Positives = 237/475 (49%), Gaps = 25/475 (5%) Query: 1 MARIAEELEKIFGPEKVVSDPHIVRLYSREPSGLEGRAEA---VVFPESAQDVSRLVRYA 57 M+ + L +I G + V++DP R Y E GL AE V P +A+ V+ +V Sbjct: 1 MSALVPRLRRICGDDGVLTDPSRRRTY--ESDGLTYHAEVPGVVALPTTAEQVAEVVGLC 58 Query: 58 YSREVYIYPQGSSTDLAGGAFPERPGVVVSMERMRRVREVSVLDSVAVVEPGVRLWDLNV 117 + V P+G+ T L+ GA P GV+V+ RMRR+ EV + AVV+PGV D+ Sbjct: 59 AAEGVPFVPRGAGTGLSAGALPRADGVLVTTSRMRRIVEVDPDNECAVVQPGVANLDITR 118 Query: 118 ELSKYRYMFPIDPGSVKVATVGGAINTGAGGMRGARYGTMRDWVLGLEIVLPDEEGTILR 177 + Y Y + DP S +V +VGG I +GG +YG + VLGL++ P +G ++R Sbjct: 119 AAAPYGYYYAPDPSSQQVCSVGGNIAENSGGAHCLKYGFTVNHVLGLQVATP--QGELVR 176 Query: 178 VGCRTLKCRQGYDLARLIVGSEGTLAIVTEAILKITPMPENVVVVLAFFPTLRQLVDAVI 237 +G + + GYDL +GSEGTL I TEA +++ P+ V +LA F + AV Sbjct: 177 LGGKAPEA-PGYDLIGAFIGSEGTLGIATEATVRLVRSPQKVTTLLAAFAGMDAGGQAVS 235 Query: 238 EVKSRAIDTLLMEFMDVDSARLAAETLGAAIRPDGHMLLVGVPVNREASTRVLEEMV--S 295 V + + +E MD S AAE A P+G ++ V ++ A+ + Sbjct: 236 SVIAEGVLPAAVEMMDALSIE-AAEAAVACDYPEGAGAVLIVELDGPAADVDADAAAVRR 294 Query: 296 IAKAAGAASVYTAKSMEEAEEKKLLEIRRSLFATQALLTQKQFKGRKVMMLMEDIAVPPS 355 + + AGA + A AE ++ + R+S FA ++ +++D VP + Sbjct: 295 LCERAGAFEIREASG--AAERARIWKGRKSAFAAVGRISP--------AYIVQDGVVPRT 344 Query: 356 KLLDAVERLKELEAKYGFKTVLGGHIGDGNLHPTISYPVDDEKAKEAALKWYYDVMRMAI 415 L + + + L A+ G + H GDGNLHP + + + A E A + ++ + I Sbjct: 345 ALGEVLGDIARLSAESGIRVANVFHAGDGNLHPLVLFDDAEPGAGERAAEVSGAILDLCI 404 Query: 416 ELGGTVSAEHGIGVLKKEALRLELERMGSVKALEIMAGIKRVFDPKGILNPGKVV 470 GG+++ EHG+GV K + RM + + LE M +R FDP G+ NP K++ Sbjct: 405 RHGGSITGEHGVGVDK----ACSMPRMFAPQDLEAMDRFRRAFDPAGVANPEKLL 455 Lambda K H 0.319 0.136 0.381 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: 540 Number of extensions: 33 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: 473 Length of database: 483 Length adjustment: 34 Effective length of query: 439 Effective length of database: 449 Effective search space: 197111 Effective search space used: 197111 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 (21.7 bits) S2: 51 (24.3 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