Align D-lactate dehydrogenase (EC 1.1.1.28); D-lactate dehydrogenase (acceptor) (EC 1.1.99.6) (characterized)
to candidate WP_012468548.1 GLOV_RS02235 FAD-linked oxidase C-terminal domain-containing protein
Query= BRENDA::Q9YEU4 (473 letters) >NCBI__GCF_000020385.1:WP_012468548.1 Length = 466 Score = 263 bits (672), Expect = 9e-75 Identities = 158/471 (33%), Positives = 250/471 (53%), Gaps = 25/471 (5%) Query: 4 IAEELEKIFGPEKVVSDPHIVRLYSREPSGLEGRAEAVVFPESAQDVSRLVRYAYSREVY 63 I EEL I GPE + ++ + Y + + +E AVV P +A++ + ++R A R Sbjct: 6 IIEELRAIVGPENLATEKQDLICYGYDATQMEFLPAAVVHPANAEETAAVLRLANQRTFP 65 Query: 64 IYPQGSSTDLAGGAFPERPGVVVSMERMRRVREVSVLDSVAVVEPGVRLWDLNVELSKYR 123 ++P+G+ + GGA P+ GVV+ RM R+ + + +A VEPGV D + K Sbjct: 66 VFPRGAGSGFTGGALPKAGGVVLVTTRMNRILRIDTENLIAEVEPGVVTEDFQKAVEKLG 125 Query: 124 YMFPIDPGSVKVATVGGAINTGAGGMRGARYGTMRDWVLGLEIVLPDEEGTILRVGCRTL 183 +P DP S+K +T+GG + AGG R +YG +D+V+GLE+VLP G I+R G T Sbjct: 126 LFYPPDPASLKFSTLGGNVAENAGGPRCVKYGVTKDFVMGLELVLP--TGEIIRTGTETY 183 Query: 184 KCRQGYDLARLIVGSEGTLAIVTEAILKITPMPENVVVVLAFFPTLRQLVDAVIEVKSRA 243 K GYDL RL+ GSEGTL ++T+ I K+ P+PE +L F ++ AV + Sbjct: 184 KAVVGYDLTRLLCGSEGTLGVITKIIFKLLPLPEAKKTMLTIFDSIDGAARAVSTIIGAK 243 Query: 244 IDTLLMEFMDVDSARLAAETLGAAIRPDGH-MLLVGVPVNREASTRVLEEMVSIAKAAGA 302 I +EFMD + + + I P+G +LL+ V +RE + + + K G Sbjct: 244 IIPTTLEFMDYATLQCVEKRFNLGIPPEGRAVLLIEVDGDRELIEKQAARIHDLIKPLGL 303 Query: 303 ASVYTAKSMEEAEEKKLLEIRRSLFATQALLTQKQFKGRKVMMLMEDIAVPPSKLLDAVE 362 AK ++AE + L ++RR + + + +F EDI VP SK+ + Sbjct: 304 VQFRAAK--DDAESEALWKVRRLVSPSLRDVNPHKFN--------EDIVVPRSKVPVVIR 353 Query: 363 RLKELEAKYGFKTVLGGHIGDGNLHPTI----SYPVDDEKAKEAALKWYYDVMRMAIELG 418 ++++++ KY V GH GDGN+H + P +EKA EA ++ + A++L Sbjct: 354 QIEKIQQKYDIPIVNFGHAGDGNIHVNVMINKEIPGQEEKAHEA----IKEIFQAALDLN 409 Query: 419 GTVSAEHGIGVLKKEALRLELERMGSVKALEIMAGIKRVFDPKGILNPGKV 469 GT+S EHG+G+ K+ + +EL + + +M GIK DP ILNPGK+ Sbjct: 410 GTMSGEHGVGLAKQPFIEMEL----TPAQIRVMQGIKLALDPNNILNPGKI 456 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: 520 Number of extensions: 27 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: 473 Length of database: 466 Length adjustment: 33 Effective length of query: 440 Effective length of database: 433 Effective search space: 190520 Effective search space used: 190520 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 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