Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_009762358.1 MICLODRAFT_RS03140 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_000262405.1:WP_009762358.1 Length = 496 Score = 318 bits (815), Expect = 3e-91 Identities = 187/480 (38%), Positives = 267/480 (55%), Gaps = 6/480 (1%) Query: 20 PTGL-FINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSS-WST 77 P GL FI+N+ V + S + +SP ++T + + SED++ AV AA +F + WS Sbjct: 17 PVGLNFIDNKAVSAASGEVMPVISPIDGTQLTVLAASDSEDMNRAVAAARRSFETGCWSG 76 Query: 78 SDPQVRMKVLYKLADLIDEHADTLAHIEALDNGKSL-MCSKGDVALTAAYFRSCAGWTDK 136 P+ R +++ K ADLID HA +A + DNG + M KG+ A R A DK Sbjct: 77 MAPRERKRIMLKWADLIDRHALEIAVLGVRDNGTDIRMALKGEPQSAADTIRFYAEAIDK 136 Query: 137 IKGSVIETGDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTP 196 G + T + RE +GV G IIPWNFPL++ SWKL P L G + V+K +E Sbjct: 137 RNGEITPTRHDILSLIHREAVGVVGVIIPWNFPLMIGSWKLAPALAAGNSVVVKPSEEAS 196 Query: 197 LSALYLASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAA 256 LS L + L EAG PPGV+N V+G G G + H + + FTGS GR +++ +A Sbjct: 197 LSILRVIELAAEAGIPPGVLNAVNGRGAIVGEALGLHMDVDVLGFTGSGGVGRRLLEYSA 256 Query: 257 ESNLKKVTLELGGKSPNIVFDDA-DVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDK 315 SNLK+V LELGGKSPN+VF DA ++K + IF N G+VC A SR+ V+ +Y Sbjct: 257 RSNLKRVYLELGGKSPNLVFADAPNLKRAARETAASIFRNNGQVCAAASRLAVERSVYKD 316 Query: 316 IVSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERF--G 373 + + A +++IGDP GA + QL K I ++GATV GG + Sbjct: 317 FMEAVRAEATAMRIGDPLSLAFTTGALANAAQLAKTRAAIARAAEQGATVYHGGNQLHAE 376 Query: 374 NKGYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHTTN 433 + G++ +PTI DV + +V+ EIFGPV+ F T EE IA+AN++ +GL++ + T + Sbjct: 377 SGGFYHEPTILTDVATEMDVVQQEIFGPVLVARSFDTEEEAIAIANETVFGLSSVLWTRD 436 Query: 434 LSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVRIGL 493 LS A VSN+I SG + +N Y+ P GG QSG G + AL+ Y +K I L Sbjct: 437 LSKAHRVSNRIKSGVVHINCYSGADITAPLGGVRQSGNGSDRSLHALEKYENLKTKWIQL 496 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: 483 Number of extensions: 20 Number of successful extensions: 5 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: 496 Length adjustment: 34 Effective length of query: 461 Effective length of database: 462 Effective search space: 212982 Effective search space used: 212982 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