Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_017549818.1 C792_RS0112615 aldehyde dehydrogenase family protein
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000330705.1:WP_017549818.1 Length = 496 Score = 296 bits (758), Expect = 1e-84 Identities = 171/473 (36%), Positives = 255/473 (53%), Gaps = 6/473 (1%) Query: 9 MYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERA--QPEWEALPAI 66 +YIDG +V G DV+NPATE VI+++ + D A+ AA +A EW + Sbjct: 21 LYIDGGYVQAHGGKMFDVLNPATEEVIAQVSEADESDIDNAVQAARKAFDAGEWTKMEPA 80 Query: 67 ERASWLRKISAGIRERASEISALIVEEGGKI-QQLAEVEVAFTADYIDYMAEWARRYEGE 125 ER+ + K + + E E++ L + GK QQ E +V T + Y A WA + G+ Sbjct: 81 ERSRLIYKFADLLEEHREELAQLEALDNGKAYQQALEDDVDGTVQHFRYYAGWATKISGK 140 Query: 126 IIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNA 185 + P +GV I+PWN+P + K+ AL G TIVIKP+ TP + Sbjct: 141 T-PNVSPDYVTYTVHEPVGVVGQIIPWNYPLAMAGWKLGAALAAGCTIVIKPASETPLSL 199 Query: 186 IAFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNI 245 + AK+ E G P GV N+V G G G L +P V V+ TGS G IM AA +I Sbjct: 200 LYAAKLFKEAGFPDGVVNVVPGAGSVAGNALVTHPGVDKVAFTGSTRTGGSIMKKAADDI 259 Query: 246 TKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRL 305 V LELGGK+PAIV++DADL+ A+ I D + N+GQ C+ R+YV + +Y++ ++ L Sbjct: 260 KSVTLELGGKSPAIVLEDADLDTALDGIFDGTMYNTGQNCSATTRIYVHRNLYEKVLDAL 319 Query: 306 GEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYY 365 + + G P MGPL++ L+ V + + EEGAR+ GG KGY+ Sbjct: 320 KDKAEKAVVG-PGLDEATDMGPLVSEKQLDTVLGYIEKGKEEGARLITGGSRKGDKGYFV 378 Query: 366 PPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMK 425 PT+ DV +M+I EE FGPV+ V FD +++ IS ANDS+YGL +S++T+N+ Sbjct: 379 EPTIFADVEDDMTIAREEIFGPVMSVFVFDEVDEVISRANDSEYGLAASVWTENIKKGHY 438 Query: 426 AIKGLKFGETYINRENFEAMQGFHAGWRKSGIG-GADGKHGLHEYLQTQVVYL 477 L+ G ++N E G++KSGIG G +G+ Y++ + V++ Sbjct: 439 IAGKLESGTVWVNDFGLELETMPFGGYKKSGIGREMGGDYGISNYVEVKSVFV 491 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: 609 Number of extensions: 35 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: 496 Length adjustment: 34 Effective length of query: 445 Effective length of database: 462 Effective search space: 205590 Effective search space used: 205590 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 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