Align Benzoyl-CoA oxygenase component A; Benzoyl-CoA 2,3-dioxygenase subunit A; Benzoyl-CoA dioxygenase reductase component; EC 1.14.13.208 (characterized)
to candidate Ac3H11_3083 Benzoyl-CoA oxygenase component A
Query= SwissProt::Q9AIX6 (414 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_3083 Length = 422 Score = 508 bits (1308), Expect = e-148 Identities = 245/419 (58%), Positives = 299/419 (71%), Gaps = 9/419 (2%) Query: 5 AEHANLARQHLIDPEICIRCNTCEEICPVDAITHDSRNYVVKFETCNGCLACISPCPTGA 64 A A + +QHLIDPEICIRCNTCE CPV AITHD NYVV+ + CNGC+ACISPCPTG+ Sbjct: 4 AVEAAVIKQHLIDPEICIRCNTCEATCPVGAITHDDNNYVVRADVCNGCMACISPCPTGS 63 Query: 65 IDSWRNVDKATPHSLADQYSWDYLPDTTELDQF--EATVMGAAELP-----AEVQQITEV 117 ID+WR + A +++ +Q +W+ LP D E A +P A V+ T+ Sbjct: 64 IDNWRTMPLARAYTIEEQLTWEELPPELPPDALAAEGVAPSADAVPPTTPAAPVEPGTQA 123 Query: 118 ATAGQGGPAMAPWSASHPYVNLYTPANPITATVTGNYRLTAEDASSDIHHIVLDFGTTPF 177 + Q G + PWSA+HPY NL+ P +P ATV GN+ T ++ HH+VLDFG+ PF Sbjct: 124 FRSAQYGATVPPWSAAHPYTNLFPPKSPTEATVVGNFNCTEAGFENETHHVVLDFGSMPF 183 Query: 178 PVLEGQSIGIIPPGVDEKGKPHLLRMYSVASPRDGERPHYNNLSLTVKRVVEDHEGNPTR 237 PVLEGQSIGIIPPG D GK H R YS+ASPR+GERP YNNL+LTVKRV DH+GN R Sbjct: 184 PVLEGQSIGIIPPGTDALGKEHHARQYSIASPRNGERPGYNNLALTVKRVTTDHDGNAVR 243 Query: 238 GVASNYVCDLKKGDKVQVTGPYGSTYLMPNHPGSSIMMICTGTGSAPMRAMTE--RRRRR 295 G+ASN+VCDLK GDKVQV GP+GS++LMPNHP S I+MICTGTGSAPMRAMTE RR R Sbjct: 244 GIASNFVCDLKVGDKVQVVGPFGSSFLMPNHPRSHIVMICTGTGSAPMRAMTEWRRRLRS 303 Query: 296 MDRKEGGELVLFFGARAPEELPYFGPLQKLPKEFIDINFAFSRVPGEPKRYVQDAIRERA 355 + EGG+L+LFFGAR +ELPYFGPLQ LPK+FIDIN AFSR G+PKRYVQD +RERA Sbjct: 304 SGKFEGGKLMLFFGARTQQELPYFGPLQNLPKDFIDINLAFSRTAGQPKRYVQDLMRERA 363 Query: 356 DKVFQMLQDDNCYIYICGLKGMEAGVLEAFRDICRAKGADWDALRPQLLSKARFHVETY 414 + +L+D + + Y+CGLK ME GV+ A RDI G DWD + L + R H+ETY Sbjct: 364 ADLAALLRDGSGHFYVCGLKSMEEGVVMALRDIASEAGLDWDTVGAALQREGRLHLETY 422 Lambda K H 0.319 0.136 0.425 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: 624 Number of extensions: 20 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: 414 Length of database: 422 Length adjustment: 32 Effective length of query: 382 Effective length of database: 390 Effective search space: 148980 Effective search space used: 148980 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: 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