Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_008506742.1 BIBO1_RS10835 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_000182725.1:WP_008506742.1 Length = 505 Score = 352 bits (903), Expect = e-101 Identities = 206/484 (42%), Positives = 284/484 (58%), Gaps = 15/484 (3%) Query: 22 GLFINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDPQ 81 G FI ++V+ +S + F SP + + +V + + D++ A++AA AA W + Sbjct: 19 GNFIGGKWVEPRSGRYFENTSPVNGQVLCEVARSDAADVEAALDAAHAA-KELWGRTSVA 77 Query: 82 VRMKVLYKLADLIDEHADTLAHIEALDNGKSLM-CSKGDVALTAAYFRSCAGWTDKIKGS 140 R +L ++AD I+E+ LA E DNGK + + D+ L +FR AG +G Sbjct: 78 ERALILNRIADRIEENLPALAAAETWDNGKPIRETTNADLPLAVDHFRYFAGVIRAQEGG 137 Query: 141 VIETGDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSAL 200 + E Y EP+GV GQIIPWNFPLLMA+WKL P L G VLK AE TP S L Sbjct: 138 ISEIDHDTVAYHFHEPLGVVGQIIPWNFPLLMATWKLAPALAAGNCVVLKPAEQTPASIL 197 Query: 201 YLASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAESNL 260 L LI + PPGVVN+V+GFG AG P++S P+I K+AFTG T TGR IM+ A++ NL Sbjct: 198 VLMELIADI-LPPGVVNIVNGFGLEAGKPLASSPRIAKIAFTGETTTGRLIMQYASQ-NL 255 Query: 261 KKVTLELGGKSPNIVFDD--ADVKSTIQHLVTGIFY---NTGEVCCAGSRIYVQEGIYDK 315 VTLELGGKSPNI F D A+ + + G N GEVC SR +QE IYD+ Sbjct: 256 IPVTLELGGKSPNIFFKDVAAEDDDFLDKAIEGFVMFALNQGEVCTCPSRALIQESIYDR 315 Query: 316 IVSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERF--- 372 + + E++ GDP T +GAQ S QL+KIL Y+DIG++EGA V+ GGER Sbjct: 316 FMEKALKRVEAIVQGDPLDPATMIGAQASSEQLEKILSYLDIGRQEGAEVLAGGERNMLP 375 Query: 373 GNK--GYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVH 430 G+ GY++KPT+F + +I ++EIFGPVV++ FK E +++AND+ YGL AG+ Sbjct: 376 GDLAGGYYVKPTVFKGHNK-MRIFQEEIFGPVVSVATFKDDAEALSIANDTLYGLGAGIW 434 Query: 431 TTNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVR 490 T + + A I +G +W N Y+ + FGGY QSGIGRE + LD+Y K + Sbjct: 435 TRDGTRAYRFGRAIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRENHLKMLDHYQNTKNML 494 Query: 491 IGLS 494 + S Sbjct: 495 VSYS 498 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: 584 Number of extensions: 26 Number of successful extensions: 8 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: 505 Length adjustment: 34 Effective length of query: 461 Effective length of database: 471 Effective search space: 217131 Effective search space used: 217131 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 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