Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_068106355.1 I601_RS03205 aldehyde dehydrogenase family protein
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_001653335.1:WP_068106355.1 Length = 472 Score = 288 bits (738), Expect = 2e-82 Identities = 173/476 (36%), Positives = 269/476 (56%), Gaps = 19/476 (3%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 Y+DG + G ++V + A +V++R AED +A AA RA P W A P +RA Sbjct: 8 YVDGAWAPGTGSTEVEVSSAADGSVLTRFQGAGAEDVARACAAAGRAWPGWAATPVTDRA 67 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVE----VAFTADYIDYMAEWARRYEGE 125 LR + + +RA E+ A +E G ++A + VA T M + A + E Sbjct: 68 DLLRTAAELVEKRADELGATAAQEVGTPIRMAPIVHGHMVAAT------MRDVADKVESH 121 Query: 126 IIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNA 185 + +R G +++L + ++GV I WN+P + +A K+ PAL G T+V+KPSE P Sbjct: 122 TFE-ERVGSSLVL-RESVGVAAAITAWNYPLYQLATKLVPALAVGCTVVLKPSEIAPLTT 179 Query: 186 IAFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNI 245 I F + + E GLP GV NLV+G G G+ L +P+V VS TGS G +I AA + Sbjct: 180 IGFFEALAEAGLPGGVANLVVGTGAEAGEPLVTDPRVGAVSFTGSTRTGVRIAELAAAGV 239 Query: 246 TKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRL 305 T+V LELGGK+ ++++DDADL AV A ++ ++N+GQ C R+ V + + L Sbjct: 240 TRVTLELGGKSASVLLDDADLATAVPATLNGCLLNNGQTCAALTRLIVPRARLAEVEEIL 299 Query: 306 GEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGG----KAVEGK 361 A+ ++ G+P + D A+GP+ +AA RV Q + A+++GA V GG + V Sbjct: 300 AAAVAQLRVGDPRD-PDTAVGPVASAAQHHRVLQHLRGALDDGATVVSGGLDAPEGVPAG 358 Query: 362 GYYYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLN 421 GYY PT +L V M I EE FGPVL V+A D+ ++A+++AND+DYGL+ ++++ + + Sbjct: 359 GYYVRPT-VLRVEPSMRIAREEVFGPVLCVIAVDSEDEAVAVANDTDYGLSGAVWSADPD 417 Query: 422 VAMKAIKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYL 477 A+ + L+ G+ +N F F G+++SG G G+ GL EYL+T+ V L Sbjct: 418 RALAVARRLRTGQVAVNGGAFNISAPF-GGYKRSGYGREGGRFGLDEYLETKAVQL 472 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: 507 Number of extensions: 25 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: 472 Length adjustment: 33 Effective length of query: 446 Effective length of database: 439 Effective search space: 195794 Effective search space used: 195794 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 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