Align Aldehyde dehydrogenase family 2 member B4, mitochondrial; ALDH2a; EC 1.2.1.3 (characterized)
to candidate WP_009762358.1 MICLODRAFT_RS03140 aldehyde dehydrogenase family protein
Query= SwissProt::Q9SU63 (538 letters) >NCBI__GCF_000262405.1:WP_009762358.1 Length = 496 Score = 350 bits (899), Expect = e-101 Identities = 190/468 (40%), Positives = 275/468 (58%), Gaps = 3/468 (0%) Query: 62 INGNFVDSASGKTFPTLDPRTGEVIAHVAEGDAEDINRAVKAARTAFDEGPWPKMSAYER 121 I+ V +ASG+ P + P G + +A D+ED+NRAV AAR +F+ G W M+ ER Sbjct: 23 IDNKAVSAASGEVMPVISPIDGTQLTVLAASDSEDMNRAVAAARRSFETGCWSGMAPRER 82 Query: 122 SRVLLRFADLVEKHSEELASLETWDNGKPYQQSLTAEIPMFARLFRYYAGWADKIHGLTI 181 R++L++ADL+++H+ E+A L DNG + +L E A R+YA DK +G Sbjct: 83 KRIMLKWADLIDRHALEIAVLGVRDNGTDIRMALKGEPQSAADTIRFYAEAIDKRNGEIT 142 Query: 182 PADGNYQVHTLHEPIGVAGQIIPWNFPLLMFAWKVGPALACGNTIVLKTAEQTPLTAFYA 241 P + E +GV G IIPWNFPL++ +WK+ PALA GN++V+K +E+ L+ Sbjct: 143 PTRHDILSLIHREAVGVVGVIIPWNFPLMIGSWKLAPALAAGNSVVVKPSEEASLSILRV 202 Query: 242 GKLFLEAGLPPGVLNIVSGFGATAGAALASHMDVDKLAFTGSTDTGKVILGLAANSNLKP 301 +L EAG+PPGVLN V+G GA G AL HMDVD L FTGS G+ +L +A SNLK Sbjct: 203 IELAAEAGIPPGVLNAVNGRGAIVGEALGLHMDVDVLGFTGSGGVGRRLLEYSARSNLKR 262 Query: 302 VTLELGGKSPFIVFEDA-DIDKAVELAHFALFFNQGQCCCAGSRTFVHEKVYDEFVEKSK 360 V LELGGKSP +VF DA ++ +A ++F N GQ C A SR V VY +F+E + Sbjct: 263 VYLELGGKSPNLVFADAPNLKRAARETAASIFRNNGQVCAAASRLAVERSVYKDFMEAVR 322 Query: 361 ARALKRVVGDPFRKGIEQGPQIDLKQFEKVMKYIKSGIESNATLECGGDQIGDK--GYFI 418 A A +GDP G + Q K I E AT+ GG+Q+ + G++ Sbjct: 323 AEATAMRIGDPLSLAFTTGALANAAQLAKTRAAIARAAEQGATVYHGGNQLHAESGGFYH 382 Query: 419 QPTVFSNVKDDMLIAQDEIFGPVQSILKFSDVDEVIKRANETKYGLAAGVFTKNLDTANR 478 +PT+ ++V +M + Q EIFGPV F +E I ANET +GL++ ++T++L A+R Sbjct: 383 EPTILTDVATEMDVVQQEIFGPVLVARSFDTEEEAIAIANETVFGLSSVLWTRDLSKAHR 442 Query: 479 VSRALKAGTVWVNCFDVFDAAIPFGGYKMSGNGREKGIYSLNNYLQIK 526 VS +K+G V +NC+ D P GG + SGNG ++ +++L Y +K Sbjct: 443 VSNRIKSGVVHINCYSGADITAPLGGVRQSGNGSDRSLHALEKYENLK 490 Lambda K H 0.319 0.136 0.404 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: 548 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: 538 Length of database: 496 Length adjustment: 35 Effective length of query: 503 Effective length of database: 461 Effective search space: 231883 Effective search space used: 231883 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: 52 (24.6 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