Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate GFF1170 PS417_05945 gamma-aminobutyraldehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >FitnessBrowser__WCS417:GFF1170 Length = 485 Score = 305 bits (781), Expect = 2e-87 Identities = 182/468 (38%), Positives = 263/468 (56%), Gaps = 5/468 (1%) Query: 4 PVQHPMYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEAL 63 P+ + IDG+ V +G A ++NPAT V+++I + AE AI AA RA W Sbjct: 7 PLLTALLIDGELVHGQGFAE-PILNPATGEVLTQIAEASAEQVETAILAAHRAFAGWSRT 65 Query: 64 PAIERASWLRKISAGIRERASEISALIVEEGGKIQQLA-EVEVAFTADYIDYMAEWARRY 122 +R++ L I+ I ++A ++ L GK LA + +++ T D + A R Sbjct: 66 TPQQRSNILLGIADAIEKQADYLARLESLNCGKPLHLARQDDLSATVDVFRFFAGAVRCQ 125 Query: 123 EGEIIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTP 182 G++ PG ++ + +GV I PWN+P + A K+APAL GNT+V KPSE TP Sbjct: 126 TGQLSGEYLPGYTSMVRRDPIGVVASIAPWNYPLMMAAWKIAPALAAGNTLVFKPSEHTP 185 Query: 183 NNAIAFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAA 242 + +A A ++ E+ LPRGV N++ G GE VG L +PKV MVS+TG + G+KI+ A+ Sbjct: 186 LSILALAPVLKEL-LPRGVINILCGGGEGVGSHLVSHPKVRMVSLTGDIVTGQKILQAAS 244 Query: 243 KNITKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFV 302 K + + LELGGKAP IV +DADL V + N+GQ C A R+Y Q GI+D+ V Sbjct: 245 KTLKRTHLELGGKAPVIVCNDADLHAVVDGVRAYGYYNAGQDCTAACRIYAQAGIHDKLV 304 Query: 303 NRLGEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAV-EGK 361 LG A+ +++F + D +GPLI+ +RV V RA+ + G AV G Sbjct: 305 AELGAAVSSLRFAGKRDA-DNELGPLISTRQRDRVASFVERALGQPHIERITGAAVHSGA 363 Query: 362 GYYYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLN 421 G+YY PTLL +Q I+ E FGPV+ V FD LE A+ ANDS+YGL SS++TQNL+ Sbjct: 364 GFYYQPTLLAGCKQNDEIVQREVFGPVVTVTRFDELEQAVDWANDSEYGLASSVWTQNLD 423 Query: 422 VAMKAIKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEY 469 AM+ L++G T+IN + H G ++SG G L +Y Sbjct: 424 KAMQVAARLQYGCTWINSHFMLVSEMPHGGLKRSGYGKDLSSDSLQDY 471 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: 528 Number of extensions: 14 Number of successful extensions: 4 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: 485 Length adjustment: 34 Effective length of query: 445 Effective length of database: 451 Effective search space: 200695 Effective search space used: 200695 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: 52 (24.6 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