Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate SMc00833 SMc00833 glycolate oxidase subunit protein
Query= reanno::Smeli:SMc00833 (405 letters) >lcl|FitnessBrowser__Smeli:SMc00833 SMc00833 glycolate oxidase subunit protein Length = 405 Score = 786 bits (2030), Expect = 0.0 Identities = 405/405 (100%), Positives = 405/405 (100%) Query: 1 MIVHFEPASEEGIASVVRSAAAERVTLAVVGGGTRAGLGNPVRADRTLSTRRLSGIVTYD 60 MIVHFEPASEEGIASVVRSAAAERVTLAVVGGGTRAGLGNPVRADRTLSTRRLSGIVTYD Sbjct: 1 MIVHFEPASEEGIASVVRSAAAERVTLAVVGGGTRAGLGNPVRADRTLSTRRLSGIVTYD 60 Query: 61 PAEMTMSALAGTPVAEVEAALHAKGQMLSFEPMDHRPIFATTGEPTIGGVFAANVSGPRR 120 PAEMTMSALAGTPVAEVEAALHAKGQMLSFEPMDHRPIFATTGEPTIGGVFAANVSGPRR Sbjct: 61 PAEMTMSALAGTPVAEVEAALHAKGQMLSFEPMDHRPIFATTGEPTIGGVFAANVSGPRR 120 Query: 121 YVAGAARDSLLGVRFVNGRGEPIKAGGRVMKNVTGLDLVKLMAGSYGTLGILTEVTFKVL 180 YVAGAARDSLLGVRFVNGRGEPIKAGGRVMKNVTGLDLVKLMAGSYGTLGILTEVTFKVL Sbjct: 121 YVAGAARDSLLGVRFVNGRGEPIKAGGRVMKNVTGLDLVKLMAGSYGTLGILTEVTFKVL 180 Query: 181 PLPPAAATVVVSGLNDAEAAAVMAEAMAQPVEVSGASHLPESVRSRFLDGALPDGAATVL 240 PLPPAAATVVVSGLNDAEAAAVMAEAMAQPVEVSGASHLPESVRSRFLDGALPDGAATVL Sbjct: 181 PLPPAAATVVVSGLNDAEAAAVMAEAMAQPVEVSGASHLPESVRSRFLDGALPDGAATVL 240 Query: 241 RLEGLAASVAIRAEKLGEKLSRFGRISQLDEAQTRTLWAEIRDVKPYADGTRRPLWRISV 300 RLEGLAASVAIRAEKLGEKLSRFGRISQLDEAQTRTLWAEIRDVKPYADGTRRPLWRISV Sbjct: 241 RLEGLAASVAIRAEKLGEKLSRFGRISQLDEAQTRTLWAEIRDVKPYADGTRRPLWRISV 300 Query: 301 APSAGHQLVAALRLQTGVDAFYDWQGGLVWLRMEADPEAELLRRYIGAVGGGHAALLRAG 360 APSAGHQLVAALRLQTGVDAFYDWQGGLVWLRMEADPEAELLRRYIGAVGGGHAALLRAG Sbjct: 301 APSAGHQLVAALRLQTGVDAFYDWQGGLVWLRMEADPEAELLRRYIGAVGGGHAALLRAG 360 Query: 361 EEARGRIPAFEPQPPAVARLSERIRAQFDPSGIFNPGRAAALVRN 405 EEARGRIPAFEPQPPAVARLSERIRAQFDPSGIFNPGRAAALVRN Sbjct: 361 EEARGRIPAFEPQPPAVARLSERIRAQFDPSGIFNPGRAAALVRN 405 Lambda K H 0.318 0.134 0.387 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: 804 Number of extensions: 23 Number of successful extensions: 3 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: 405 Length of database: 405 Length adjustment: 31 Effective length of query: 374 Effective length of database: 374 Effective search space: 139876 Effective search space used: 139876 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 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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