Align acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized)
to candidate AZOBR_RS32475 AZOBR_RS32475 aldehyde Dehydrogenase
Query= BRENDA::A0A0H3W5K4 (859 letters) >FitnessBrowser__azobra:AZOBR_RS32475 Length = 475 Score = 238 bits (607), Expect = 6e-67 Identities = 147/446 (32%), Positives = 244/446 (54%), Gaps = 16/446 (3%) Query: 11 QKQIDLLVSRAQEAQKKFMSYTQEQIDAIVKAMALAGVD--KHVELAKMAYEETKMGVYE 68 Q+ I LV+RA+ AQ+ F TQE++D V A+A A + + LA++A +T +G Sbjct: 15 QEAIAALVARARTAQRAFADATQERVDDAVAALAWAIYEPGRARALAELAVADTGLGNVA 74 Query: 69 DKITKNLFATEYVYHDIKNEKTVGIINENIEENYMEVAEPIGVIAGVTPVTNPTSTTMFK 128 DKI KN T D+ +TVG+I E+ + +++A+P+GV+ VTP TNP +T + K Sbjct: 75 DKIVKNQRKTFGTLRDLMRVRTVGVIEEDTAKGIVKIAKPLGVVGAVTPSTNPAATPVNK 134 Query: 129 CLISIKTRNPIIFSFHPKAIKCSIAAAKVMYEAALKAGAPEGCIGWIETPSIEA-TQLLM 187 ++++K RN II + P + ++M + GAPE + I TP + TQ LM Sbjct: 135 AMMAVKGRNAIIIAPSPMGSAATGRTVELMRAELARIGAPEDLVQMIPTPITKGLTQALM 194 Query: 188 THPGVSLILATGGAGMVKAAYSSGKPALGVGPGNVPCYIEKSANIKRAVSDLILSKTFDN 247 V L++ TG V+ AYSSG PA+GVG GNVP +++SA++ A + SKTFDN Sbjct: 195 --EAVDLVVVTGSQDNVRRAYSSGTPAIGVGAGNVPVIVDESADLAEAARKIGASKTFDN 252 Query: 248 GVICASEQAVIIDEEIADEVKKLMKEYGCYFLNKDEIKKL-----EKFAIDEQSCAMSPA 302 C+SE A+++ + + D ++E G + +E +++ E ++ + A PA Sbjct: 253 STSCSSENALVVLDSVYDATIAALEEAGAHLCTPEERERVQSRLWENGKLNRKLIAKDPA 312 Query: 303 VVGQPAAKIAEMAGFKVPEGTKILVAEYEGVGPKYPLSREKLSPILACYTVKDYNEGIKK 362 ++ + A ++A A + + E GVG +P S EKLS +LA Y V D++ + + Sbjct: 313 ILAE-AFELAPKA-----REARFFLVEETGVGKAHPFSGEKLSLVLAVYRVPDFDAAVDQ 366 Query: 363 CEEMTEFGGLGHSAVIHSENQNVINEFARRVRTGRLIVNSPSSQGAIGDIYNTNTPSLTL 422 ++ + G GHS IH+ ++ A + R++VN + G G + +L++ Sbjct: 367 VRKILDHQGRGHSCGIHTRDEAHAKRLADELDVVRVLVNFAHTFGNGGGFDSGLNFTLSM 426 Query: 423 GCGSMGRNSTTDNVSVKNLLNIKRVV 448 GCGS +NS ++N+S K+ +NI +V Sbjct: 427 GCGSWQKNSISENLSWKHFVNITHLV 452 Lambda K H 0.317 0.134 0.382 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: 784 Number of extensions: 42 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: 859 Length of database: 475 Length adjustment: 38 Effective length of query: 821 Effective length of database: 437 Effective search space: 358777 Effective search space used: 358777 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 (21.6 bits) S2: 54 (25.4 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