Align D-lactate dehydrogenase (EC 1.1.1.28); D-lactate dehydrogenase (acceptor) (EC 1.1.99.6) (characterized)
to candidate WP_035245160.1 G494_RS0101860 FAD-linked oxidase C-terminal domain-containing protein
Query= BRENDA::Q9YEU4 (473 letters) >NCBI__GCF_000429965.1:WP_035245160.1 Length = 467 Score = 236 bits (603), Expect = 9e-67 Identities = 150/466 (32%), Positives = 250/466 (53%), Gaps = 19/466 (4%) Query: 6 EELEKIFGPEKVVSDPHIVRLYSREPSGLEGRAEAVVFPESAQDVSRLVRYAYSREVYIY 65 +ELE IF E V++ + YS + S +E R EAVVF + + +S L+++AY + + Sbjct: 7 KELEAIFSKENVLTAQEDMIAYSYDASHVEIRPEAVVFATTTEQISALMKFAYREHLPVT 66 Query: 66 PQGSSTDLAGGAFPERPGVVVSMERMRRVREVSVLDSVAVVEPGVRLWDLNVELSKYRYM 125 P+G + L+GG+ P G+V+ M+RM+RV E + + VE G+ D++ + Sbjct: 67 PRGQGSGLSGGSVPLNRGIVLCMDRMKRVIEFDPANRLITVEAGLTTADIDPVAGEANLF 126 Query: 126 FPIDPGSVKVATVGGAINTGAGGMRGARYGTMRDWVLGLEIVLPDEEGTILRVGCRTLKC 185 +P DPGSV +T+GG + AGG+RG +YG +D+V +++VLP +G I+ +G + +K Sbjct: 127 YPPDPGSVAFSTIGGNVAENAGGLRGLKYGVTKDYVKMMKVVLP--QGDIVTMGNKCVKH 184 Query: 186 RQGYDLARLIVGSEGTLAIVTEAILKITPMPENVVVVLAFFPTLRQLVDAVIEVKSRAID 245 G+++ + VGSEG L I+TE L + P+P++ LA F +L AV ++ + + Sbjct: 185 VAGFNMEGIFVGSEGLLGIMTEVTLALLPIPKHRESALAIFNSLDGAAQAVSDIIASGVT 244 Query: 246 TLLMEFMDVDSARLAAETLGAAIRPDGHMLLVGVPVNREASTRVLE--EMVSIAKAAGAA 303 MEFMD + + D +L+ + + E + V E ++ K Sbjct: 245 PSTMEFMDNATINAIQNFKDCGLPRDAAAVLL-IETDGEEHSAVFEMAQVEIQVKKNDIR 303 Query: 304 SVYTAKSMEEAEEKKLLEIRRSLFATQALLTQKQFKGRKVMMLMEDIAVPPSKLLDAVER 363 AKS EE + +L E RR A AL + K +++ED V S+L + V Sbjct: 304 EFSRAKSSEERD--RLFEGRR--VALNALASVKP------NLILEDATVMRSRLPEMVRG 353 Query: 364 LKELEAKYGFKTVLGGHIGDGNLHPTISYPVDDEKAKEAALKWYYDVMRMAIELGGTVSA 423 + ++ +Y + + GH GDGNLHPT + D++ + + ++AI+L GT+S Sbjct: 354 ITDIAQQYQLQVGIFGHAGDGNLHPTFLVDMRDKEEMARTEQGVTALFQLAIDLEGTISG 413 Query: 424 EHGIGVLKKEALRLELERMGSVKALEIMAGIKRVFDPKGILNPGKV 469 EHGIG+ KK LR ++ + + ++ IK+ FDP +LNPGK+ Sbjct: 414 EHGIGLEKKPFLRNQI----GAEGIRLLQDIKKTFDPLNLLNPGKM 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: 451 Number of extensions: 22 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: 467 Length adjustment: 33 Effective length of query: 440 Effective length of database: 434 Effective search space: 190960 Effective search space used: 190960 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