Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_109969072.1 DK846_RS11355 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_003173355.1:WP_109969072.1 Length = 475 Score = 290 bits (742), Expect = 8e-83 Identities = 160/465 (34%), Positives = 248/465 (53%), Gaps = 6/465 (1%) Query: 31 QSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDPQVRMKVLYKL 90 + + T ++P+T E + +V + D+D AV +A+ AF W+ D R KVL+ Sbjct: 11 EHEHSNTIPVINPATGELVGKVNSGTAGDVDAAVTSASEAF-PKWAVKDGTERAKVLFGA 69 Query: 91 ADLIDEHADTLAHIEALDNGKSLMCSKGDVALTAAYFRSCAGWTDKIKGSVIETGDTHFN 150 A L+ LA++ + GK L SK ++A A A + +KG + Sbjct: 70 AALVRSRQADLANLLTREQGKPLKESKNEIAGFAKILEYYASISGLLKGDYGHSSAYGHA 129 Query: 151 YTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSALYLASLIKEAG 210 R P+GVCG IIPWN P ++ WK+GP L +G VLK A + PL+ + L + EAG Sbjct: 130 IVSRNPLGVCGAIIPWNVPAIIMGWKVGPALASGNALVLKPATTAPLTCMQLVGCLVEAG 189 Query: 211 APPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAESNLKKVTLELGGK 270 P ++ +V+G GP G I+ HP ++ V+FTG ATGR + AA K++TLELGG Sbjct: 190 LPGNILQIVTGPGPVVGEAIAEHPDVRAVSFTGEVATGRRVASLAAPL-FKRITLELGGS 248 Query: 271 SPNIVFDDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDKIVSEFKNAAESLKIG 330 P IV DAD+ + V G F+N G+ C A R++V+ + ++ V + + SLK+G Sbjct: 249 DPMIVCKDADLTVAAKGAVAGRFFNCGQTCTAVKRLFVESSVEEEFVHKLETLIRSLKVG 308 Query: 331 DPFKEDTFMGAQTSQLQLDKILKYIDIGKKEG-ATVITGGERFG---NKGYFIKPTIFGD 386 + D MG S Q I I+ G + TGG+ G + G+F +PT+ Sbjct: 309 NGLGSDVDMGPIHSLAQQHLISGQIERTVDGGFGKITTGGKEIGEGDHTGFFFEPTLLSG 368 Query: 387 VKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHTTNLSTAISVSNKINS 446 + + ++R+E+FGPV+ + F ++++ I+ AN +++GL A V T + ++ + Sbjct: 369 LDPEAPVMREEVFGPVLPVMPFDSLDDAISAANSTQFGLGASVWTHDSRVISRACEELQA 428 Query: 447 GTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVRI 491 G +WVN + P VPFGG SGIGRE G ALD+Y + K + I Sbjct: 429 GIVWVNQHLKLPPEVPFGGTKDSGIGRENGRYALDHYLEEKTILI 473 Lambda K H 0.316 0.133 0.389 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: 596 Number of extensions: 30 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: 495 Length of database: 475 Length adjustment: 34 Effective length of query: 461 Effective length of database: 441 Effective search space: 203301 Effective search space used: 203301 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: 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