Align acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized)
to candidate BWI76_RS20790 BWI76_RS20790 aldehyde dehydrogenase
Query= metacyc::STM2463-MONOMER (467 letters) >FitnessBrowser__Koxy:BWI76_RS20790 Length = 467 Score = 871 bits (2250), Expect = 0.0 Identities = 450/467 (96%), Positives = 459/467 (98%) Query: 1 MNQQDIEQVVKAVLLKMKDSSQPASTVHEMGVFASLDDAVAAAKRAQQGLKSVAMRQLAI 60 MNQQDIEQVVKAVLLKM DSS+P STVHEMGVFASLDDAVAAAK AQQGLKSVAMRQLAI Sbjct: 1 MNQQDIEQVVKAVLLKMTDSSKPDSTVHEMGVFASLDDAVAAAKVAQQGLKSVAMRQLAI 60 Query: 61 HAIREAGEKHARELAELAVSETGMGRVDDKFAKNVAQARGTPGVECLSPQVLTGDNGLTL 120 HAIREAGEK+ARELAELAVSETGMGRV+DKFAKNVAQARGTPGVECLSPQVLTGDNGLTL Sbjct: 61 HAIREAGEKYARELAELAVSETGMGRVEDKFAKNVAQARGTPGVECLSPQVLTGDNGLTL 120 Query: 121 IENAPWGVVASVTPSTNPAATVINNAISLIAAGNSVVFAPHPAAKKVSQRAITLLNQAVV 180 IENAPWGVVASVTPSTNPAATVINNAISLIAAGNSVVFAPHPAAKKVSQRAI LLNQAV+ Sbjct: 121 IENAPWGVVASVTPSTNPAATVINNAISLIAAGNSVVFAPHPAAKKVSQRAIMLLNQAVI 180 Query: 181 AAGGPENLLVTVANPDIETAQRLFKYPGIGLLVVTGGEAVVDAARKHTNKRLIAAGAGNP 240 AAGGP NLLVTVANPDIETAQRLFKYPGIGLLVVTGGEAVV++ARKHTNKRLIAAGAGNP Sbjct: 181 AAGGPANLLVTVANPDIETAQRLFKYPGIGLLVVTGGEAVVESARKHTNKRLIAAGAGNP 240 Query: 241 PVVVDETADLPRAAQSIVKGASFDNNIICADEKVLIVVDSVADELMRLMEGQHAVKLTAA 300 PVVVDETADL RAAQSIVKGASFDNNIICADEKVLIVVDSVADELMRLMEGQ AVKLTAA Sbjct: 241 PVVVDETADLARAAQSIVKGASFDNNIICADEKVLIVVDSVADELMRLMEGQQAVKLTAA 300 Query: 301 QAEQLQPVLLKNIDERGKGTVSRDWVGRDAGKIAAAIGLNVPDQTRLLFVETPANHPFAV 360 QAEQLQPVLLKNIDERGKGTVSRDWVGRDAGKIAAAIGLNVP QTRLLFVETPA+HPFAV Sbjct: 301 QAEQLQPVLLKNIDERGKGTVSRDWVGRDAGKIAAAIGLNVPPQTRLLFVETPASHPFAV 360 Query: 361 TEMMMPVLPVVRVANVEEAIALAVQLEGGCHHTAAMHSRNIDNMNQMANAIDTSIFVKNG 420 TE+MMPVLPVVRVANV+EAIALAVQLEGGCHHTAAMHSRNIDNMNQMANAIDTSIFVKNG Sbjct: 361 TELMMPVLPVVRVANVDEAIALAVQLEGGCHHTAAMHSRNIDNMNQMANAIDTSIFVKNG 420 Query: 421 PCIAGLGLGGEGWTTMTITTPTGEGVTSARTFVRLRRCVLVDAFRIV 467 PCIAGLGLGGEGWTTMTITTPTGEGVTSARTFVRLRRCVLVDAFRIV Sbjct: 421 PCIAGLGLGGEGWTTMTITTPTGEGVTSARTFVRLRRCVLVDAFRIV 467 Lambda K H 0.317 0.131 0.370 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: 836 Number of extensions: 24 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: 467 Length of database: 467 Length adjustment: 33 Effective length of query: 434 Effective length of database: 434 Effective search space: 188356 Effective search space used: 188356 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: 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