Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate AZOBR_RS31000 AZOBR_RS31000 aldehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >FitnessBrowser__azobra:AZOBR_RS31000 Length = 479 Score = 269 bits (688), Expect = 1e-76 Identities = 173/463 (37%), Positives = 248/463 (53%), Gaps = 14/463 (3%) Query: 20 GDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERASWLRKISAGI 79 G ++V+NPATE V + G EDA++A+ AA A + P ER L + A Sbjct: 19 GATVMEVLNPATEQVSGTVALGGPEDAQRAVAAAHAAFDGFSRTPLNERLELLAAVCALF 78 Query: 80 RERASEISALIVEE-GGKIQQLAEVEVAFTA-DYIDYMAEWARRYEGEIIQSDRPGENIL 137 +R E++ I EE G + L++ AF + E AR Y E R Sbjct: 79 EKRMDEVADAITEEMGAPLAALSKPAQAFMGLAHFKTALEAAREYPFE-----RTRGTTR 133 Query: 138 LFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFAKIVDEIGL 197 + + +GV I PWN+P IA K+APAL TG T+V+KPSEF P +A FA+I+ E G+ Sbjct: 134 ILREPVGVCAMITPWNWPINQIACKVAPALATGCTMVLKPSEFAPYSAWIFAEILHEAGV 193 Query: 198 PRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVCLELGGKAP 257 P GVFN+ G G VG LA +P V MVS+TGS AG + AA +I +V LELGGK+ Sbjct: 194 PAGVFNMFYGDGAVVGPVLASHPLVDMVSLTGSTRAGASVSHNAADSIKRVSLELGGKSA 253 Query: 258 AIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAMQAVQFGNP 317 I+ + ADL AV V S + N+GQ CN R+YV D+ + + G+P Sbjct: 254 NIICESADLTKAVTHGVRSMMSNTGQSCNAPSRMYVPASRLDEAETIAAQVCARLVVGDP 313 Query: 318 AERND-IAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEG---KGYYYPPTLLLDV 373 R D +GP+ N ERV++ + +EEGA + GG +G+Y PT+ Sbjct: 314 --RGDRTGVGPIANQRQYERVQRLIQAGIEEGATLLCGGPGRPDGLERGFYAKPTVFSRA 371 Query: 374 RQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKGLKFG 433 M+IM EE FGPVL + ++ +E+AI ANDS YGL+ +Y ++ A K L+ G Sbjct: 372 TDGMTIMREEIFGPVLTIRPYEDIEEAIRSANDSLYGLSGYVYAGTVDEARAVAKRLRTG 431 Query: 434 ETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVY 476 ++N + + F G+++SGIG G+ G E+L+T+ VY Sbjct: 432 MVHLNGASIDLAAPF-GGYKQSGIGREWGEVGFEEFLETKSVY 473 Lambda K H 0.318 0.135 0.392 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: 475 Number of extensions: 19 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: 479 Length of database: 479 Length adjustment: 34 Effective length of query: 445 Effective length of database: 445 Effective search space: 198025 Effective search space used: 198025 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 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