Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_104913346.1 C3B54_RS03975 aldehyde dehydrogenase family protein
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_002950575.1:WP_104913346.1 Length = 486 Score = 274 bits (700), Expect = 6e-78 Identities = 162/478 (33%), Positives = 267/478 (55%), Gaps = 16/478 (3%) Query: 1 MSVPVQHPMYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPE- 59 +S+ ++ ++I+G+F RG + D ++PATE V++R + ED AI A A + Sbjct: 16 VSLADEYGLFINGEFRPGRGGVF-DSISPATEEVLTRFSEASEEDVDYAIGQARAAYDKV 74 Query: 60 WEALPAIERASWLRKISAGIRERASEISALIVEEGGK-IQQLAEVEVAFTADYIDYMAEW 118 W +P ER+ +L +I+ ++ER+ E++ + GK I++ +V++ A + Y A W Sbjct: 75 WSKMPGRERSKYLFRIARIVQERSRELAIAETMDNGKPIKETRDVDIPLVAAWFFYYAGW 134 Query: 119 ARRYEGEIIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPS 178 A + E E S +P A GV ++PWNFP ++A K+APAL GNT+V+KP+ Sbjct: 135 ADKLE-EATGSHQP--------HAWGVVGQVIPWNFPLMMLAWKVAPALAAGNTVVLKPA 185 Query: 179 EFTPNNAIAFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIM 238 E T A+ FA+I + G+P GV N+V G G T G+ L + + V+ TGS G +I Sbjct: 186 ETTSVTAMLFAEICQQAGVPAGVVNIVTGAGAT-GRALVSHAGIDKVAFTGSTPVGREIA 244 Query: 239 ATAAKNITKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIY 298 T A T + LELGGK IV DDA ++ AV+ I+ N G VC R+ VQ+ ++ Sbjct: 245 KTLAGRPTALTLELGGKGANIVFDDAAMDEAVEGIISGIFFNQGHVCCAGSRLLVQENVH 304 Query: 299 DQFVNRLGEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAV 358 D+ + RL +Q ++ G+P ++N +G + + A L+ + V+EGA + A+ Sbjct: 305 DELLARLTSRIQTLRLGDPLDKN-TDIGAINSRAQLDTISTLTQSGVDEGASIWQSDCAL 363 Query: 359 EGKGYYYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQ 418 +G+++PPT+ DV I +E FGPVL V+ F T ++A++ AN++ YGL++ ++T+ Sbjct: 364 PERGFWFPPTVFTDVSTSHRIAQDEIFGPVLSVLTFRTPDEAVAKANNTPYGLSAGVWTE 423 Query: 419 NLNVAMKAIKGLKFGETYINREN-FEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVV 475 + + + L+ G + N N F+ F G+++SG G G GL YL+ V Sbjct: 424 KASRMLAVVDRLRAGVVWSNTFNKFDPTSPF-GGYQESGYGREGGLPGLLSYLRPHSV 480 Lambda K H 0.318 0.135 0.392 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: 520 Number of extensions: 29 Number of successful extensions: 6 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: 479 Length of database: 486 Length adjustment: 34 Effective length of query: 445 Effective length of database: 452 Effective search space: 201140 Effective search space used: 201140 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 (21.7 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