Align D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized)
to candidate WP_069333135.1 C8J29_RS11975 FAD-binding protein
Query= reanno::Phaeo:GFF2925 (482 letters) >NCBI__GCF_003046325.1:WP_069333135.1 Length = 477 Score = 782 bits (2019), Expect = 0.0 Identities = 388/475 (81%), Positives = 422/475 (88%) Query: 1 MEMPIPDQTVLSQKTELALRLAAVLPDDALVQDPAETRAYECDALTAYKCPPMLVVLPRT 60 M MP PDQ VL++K + RL AVLP DA++ D AETRAYECDALTAY+CPP+ VLPR+ Sbjct: 1 MLMPPPDQAVLARKARIVERLLAVLPADAVIHDEAETRAYECDALTAYRCPPLAAVLPRS 60 Query: 61 TKEVSDVLRICHAAGVPVVPRGAGTSLAGGALPTADCVILGVARMNAVLETDYDNRIIRV 120 T EVS VLRICH VPVVPRG+GTSLAGGALPTADCVILGVARMN VLETDY +R IRV Sbjct: 61 TAEVSAVLRICHEERVPVVPRGSGTSLAGGALPTADCVILGVARMNRVLETDYADRFIRV 120 Query: 121 QTGRTNLSVSGAVEEEEFFYAPDPSSQLACAIAGNIAMNSGGAHCLKYGVTTNNLMGVTM 180 +TGRTNLSV+GAVE + FFYAPDPSSQLACAIAGNIAMNSGGAHCLKYGVTTNNL+GVTM Sbjct: 121 ETGRTNLSVTGAVEVDGFFYAPDPSSQLACAIAGNIAMNSGGAHCLKYGVTTNNLLGVTM 180 Query: 181 VMMDGTVVEIGGAHLDAGGLDLLGVICGSEGQLGVVTEATLRILRKPEGARPVLIGYDSN 240 V+MDGTVVEIGGAHLDA GLDLLGVICGSEGQLGVVTEATLRIL KPEGARPVL+G+ SN Sbjct: 181 VLMDGTVVEIGGAHLDAPGLDLLGVICGSEGQLGVVTEATLRILPKPEGARPVLMGFGSN 240 Query: 241 EVAGACVSDIIKAGVLPVAIEFMDRPCIEACEAFAKAGYPMCEALLIVEVEGSDAEIDHQ 300 EVAGACVSDII+AG+LPVAIEFMDRPCI A EAFA+AGYP CEALLIVEVEGS AEID Q Sbjct: 241 EVAGACVSDIIRAGILPVAIEFMDRPCIRATEAFARAGYPDCEALLIVEVEGSPAEIDDQ 300 Query: 301 LRLITEIARSHNPVELREARDSDEAARIWLGRKSAFGAMGQINDYMCLDGTIPVTSLPHV 360 L I EIAR H+PVELRE+R +E+ RIWLGRKSAFGAMGQINDYMCLDGTIPVT LP V Sbjct: 301 LARILEIARRHDPVELRESRSEEESRRIWLGRKSAFGAMGQINDYMCLDGTIPVTELPRV 360 Query: 361 LRRIGEMSKEFGLDVANVFHAGDGNMHPLILFDANKPGDLETCEAFGAEILKLCVEVGGC 420 LRRIGE++ E GL+VANVFHAGDGNMHPLILFDAN+PGDLE CE GAEILKLCVEVGGC Sbjct: 361 LRRIGELAAEAGLEVANVFHAGDGNMHPLILFDANRPGDLERCERLGAEILKLCVEVGGC 420 Query: 421 LTGEHGVGIEKRDLMLDQYGVADIEAQLRVKDVFDPKWLLNPAKVFPLSTTQSRR 475 LTGEHGVG+EKRDLM Q+ AD+EAQ+RVKDVFDP+WLLNPAKVFPL + RR Sbjct: 421 LTGEHGVGVEKRDLMGVQFAPADLEAQMRVKDVFDPRWLLNPAKVFPLDASGDRR 475 Lambda K H 0.320 0.137 0.408 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: 822 Number of extensions: 30 Number of successful extensions: 1 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: 482 Length of database: 477 Length adjustment: 34 Effective length of query: 448 Effective length of database: 443 Effective search space: 198464 Effective search space used: 198464 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 (21.8 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