Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_028310075.1 H566_RS0101815 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_000482785.1:WP_028310075.1 Length = 507 Score = 357 bits (917), Expect = e-103 Identities = 207/483 (42%), Positives = 295/483 (61%), Gaps = 17/483 (3%) Query: 24 FINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDPQVR 83 FIN +FV + F +SP + T+ + + DI+ A++AA AA W+ + R Sbjct: 23 FINGQFVPPVDGQYFDVISPINGKVFTKAARSNAADIELALDAAHAA-QVKWARTSHAER 81 Query: 84 MKVLYKLADLIDEHADTLAHIEALDNGKSLMCS-KGDVALTAAYFRSCAGWTDKIKGSVI 142 +L K+AD ++++ + LA+ E +DNGK + + D+ L +FR AG +G++ Sbjct: 82 ANILLKIADRLEQNLERLAYAETVDNGKPIRETLNADIPLAVDHFRYFAGVLRAQEGTLS 141 Query: 143 ETGDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSALYL 202 + + Y EP+GV GQIIPWNFP+LMA+WKL P L G + VLK AESTP+S L L Sbjct: 142 QIDENTVAYHFHEPLGVVGQIIPWNFPILMAAWKLAPALGAGNSVVLKPAESTPISILVL 201 Query: 203 ASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAESNLKK 262 LI + PPGV+NVV+GFG AG P+++ +I K+AFTGSTATGR I +AAA +NL Sbjct: 202 VELIADL-LPPGVLNVVNGFGRDAGMPLATSKRIAKIAFTGSTATGRVIAQAAA-NNLIP 259 Query: 263 VTLELGGKSPNIVF------DDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDKI 316 TLELGGKSPNI F DDA + I+ +V F N GEVC + +R +QE IYD+ Sbjct: 260 ATLELGGKSPNIFFEDVMAADDAFLDKAIEGMVLFAF-NQGEVCTSPTRALIQESIYDRF 318 Query: 317 VSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGG---ERFG 373 + ++K G+P +T +GAQ S +Q DKIL YI IGK+EGA ++ GG E G Sbjct: 319 IERVLKRVAAIKQGNPLDTETQIGAQASAVQQDKILSYIGIGKEEGAQLLIGGSKPELSG 378 Query: 374 NK--GYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHT 431 + GY+++PT+F + +I ++EIFGPV+++T FK E +++AND+ YGL AGV T Sbjct: 379 DLAGGYYVQPTLFKGHNK-LRIFQEEIFGPVLSVTTFKDDAEALSIANDTVYGLGAGVWT 437 Query: 432 TNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVRI 491 + S A I +G +WVN Y+ + FGGY +SGIGRE + LD+Y Q K + + Sbjct: 438 RDGSRAYRFGRDIQAGRVWVNNYHAYPAHAAFGGYKESGIGRETHKIILDHYQQTKNMLV 497 Query: 492 GLS 494 S Sbjct: 498 SYS 500 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: 605 Number of extensions: 25 Number of successful extensions: 7 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: 507 Length adjustment: 34 Effective length of query: 461 Effective length of database: 473 Effective search space: 218053 Effective search space used: 218053 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