Align Short/branched chain specific acyl-CoA dehydrogenase, mitochondrial; SBCAD; 2-methyl branched chain acyl-CoA dehydrogenase; 2-MEBCAD; 2-methylbutyryl-coenzyme A dehydrogenase; 2-methylbutyryl-CoA dehydrogenase; EC 1.3.8.5 (characterized)
to candidate Dsui_0975 Dsui_0975 acyl-CoA dehydrogenase
Query= SwissProt::P70584 (432 letters) >lcl|FitnessBrowser__PS:Dsui_0975 Dsui_0975 acyl-CoA dehydrogenase Length = 390 Score = 246 bits (629), Expect = 7e-70 Identities = 132/373 (35%), Positives = 218/373 (58%), Gaps = 4/373 (1%) Query: 63 MMQKAVKKFAQEQIAPLVSTMDENSKMEKSVIQGLFQQGMMGIEVEAKYGGTEASFLCSV 122 M++ V+ FA ++IAP + +D +++ + Q G++G+ E +YGGT +L + Sbjct: 16 MLRDTVRAFAAKEIAPRAAQIDRDNEFPADLWQKFGDLGLLGMTAEEEYGGTAMGYLAHI 75 Query: 123 LVIEELAKVDASVALLCDIQNTVINKLFRKHGTEEQKATYLPKLVT-EKLGSFCLSEAGA 181 + +EE+++ ASV L + + R++GT QKA YLP L++ ++G+ +SE A Sbjct: 76 VAMEEISRASASVGLSYGAHSNLCVNQIRRNGTAAQKAKYLPGLISGTQVGALAMSEPNA 135 Query: 182 GSDSFALKTRADKSGNYYVINGSKMWISNAEHAELFLVFANVDPPSGYRGITCFLVDRDT 241 GSD ++K +A+K G+ YV+NGSKMWI+N A+ +V+A D +G +G+T F+V++ Sbjct: 136 GSDVVSMKLKAEKKGDRYVLNGSKMWITNGGDADTLVVYAKTDLNAGAKGMTAFIVEKGF 195 Query: 242 EGFQIGRRENKMGIRASSTCQLTFENVKVPETSVLGKIGHGYKYAIGSLNEGRIGIAAQM 301 +GF G +K+G+R S+T L F++ +VPE +VLG +G+G K + L+ R + Sbjct: 196 KGFSHGTHLDKLGMRGSNTFPLFFDDCEVPEENVLGGVGNGAKVLMSGLDYERAVLCGGP 255 Query: 302 LGLAQGCFDYTIPYIKERMQFGKRIFDFQGLQHQVAHVATQLEAARLLTY---NAARLVE 358 LG+ C D +PY+ ER QFG I +FQ +Q ++A + + +A R Y A + Sbjct: 256 LGIMAACMDVVLPYLHEREQFGTAIGEFQLMQGKLADMYSTWQATRAYVYAVGQACDRAD 315 Query: 359 AGRPFIKEASMAKYYASEVAGLTTSKCIEWMGGVGYTKDYPVEKFFRDAKIGTIYEGTSN 418 R K+A+ A Y++E A I+ +GGVGYT +YP + +RDAK+ I GTS Sbjct: 316 HARSLRKDAAGAILYSAEKATWMAGDAIQTLGGVGYTNEYPTGRLWRDAKLYEIGAGTSE 375 Query: 419 IQLNTIAKHIDAE 431 I+ I + + AE Sbjct: 376 IRRMLIGRELFAE 388 Lambda K H 0.319 0.134 0.389 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: 403 Number of extensions: 19 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: 432 Length of database: 390 Length adjustment: 31 Effective length of query: 401 Effective length of database: 359 Effective search space: 143959 Effective search space used: 143959 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