Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_047214813.1 PATSB16_RS14485 aldehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_001931675.1:WP_047214813.1 Length = 498 Score = 342 bits (878), Expect = 1e-98 Identities = 184/463 (39%), Positives = 271/463 (58%), Gaps = 6/463 (1%) Query: 38 FGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFH-SSWSTSDPQVRMKVLYKLADLIDE 96 + ++ P+ E ++ A + D +AVEAA AA+ + WS P R VL+++ADLI Sbjct: 28 YASLYPADESVNAEIAAADASDAAEAVEAADAAWRRADWSGLKPHQRAAVLHRIADLIQA 87 Query: 97 HADTLAHIEALDNGKSLMCSKGDVALTAAYFRSCAGWTDKIKGSVIETGDTHFNYTRREP 156 A+ LAH++ DNGK + ++ VA A FR A + ++ ++ + + + EP Sbjct: 88 RAEPLAHLQRRDNGKPISETRALVASAAGTFRYFAACLETLEENLTPQRGDYLSMSVHEP 147 Query: 157 IGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSALYLASLIKEAGAPPGVV 216 +GV I PWN P+ + KL P L G VLK AE TPL +L L + EAG PPGV+ Sbjct: 148 LGVIAAITPWNSPIASDAQKLAPALAAGNAVVLKPAEVTPLVSLELGRICLEAGVPPGVL 207 Query: 217 NVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAESNLKKVTLELGGKSPNIVF 276 +V+ G G G + HPK+KKVAFTG T GR I + AA+ L V+LELGGKSP +VF Sbjct: 208 SVLPGKGSIIGDALVRHPKVKKVAFTGGTEVGRGIARLAAD-KLMPVSLELGGKSPTMVF 266 Query: 277 DDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDKIVSEFKNAAESLKIGDPFKED 336 DAD+ + ++ GIF ++GE C AGSR++V ++D V A +L++GDP +ED Sbjct: 267 ADADLDHAVAGVLYGIFSSSGESCIAGSRLFVHTSVHDAFVERLVAGARALRVGDPLRED 326 Query: 337 TFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERFG----NKGYFIKPTIFGDVKEDHQ 392 T MG + I +Y+++G EG ++ GG R +KGYF PTI + + + Sbjct: 327 TQMGPLVTGAHRASIERYVELGLAEGGRLLCGGARPAGEGRDKGYFYLPTILAGLNNEAR 386 Query: 393 IVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHTTNLSTAISVSNKINSGTIWVN 452 + R+EIFGPV+ + F +++ ANDS YGLAAG+ T + A V+ + +GT+W+N Sbjct: 387 MCREEIFGPVLAVMAFDDEADLLRQANDSVYGLAAGIWTRDYKRAWRVARALETGTVWIN 446 Query: 453 TYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVRIGLSQ 495 TY F PFGG+ +SG+GRE G L YTQ K++ GL++ Sbjct: 447 TYKQFSISTPFGGWKESGVGREKGRLGLLEYTQQKSLYWGLNE 489 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: 601 Number of extensions: 25 Number of successful extensions: 3 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: 498 Length adjustment: 34 Effective length of query: 461 Effective length of database: 464 Effective search space: 213904 Effective search space used: 213904 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