Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_013721734.1 ALIDE2_RS07695 aldehyde dehydrogenase family protein
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000204645.1:WP_013721734.1 Length = 497 Score = 272 bits (696), Expect = 2e-77 Identities = 159/472 (33%), Positives = 247/472 (52%), Gaps = 4/472 (0%) Query: 9 MYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERA--QPEWEALPAI 66 + I GQ+V + +NPATE ++ R+ + + D A+ AA +A P W A+ Sbjct: 27 LLIGGQWVDAVSGKTFETLNPATEQLLCRVAEAEQADVDAAVAAARKAFEAPSWSAMSPH 86 Query: 67 ERASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEI 126 R L +I+ + E++A+ + G A AD Y A W + G Sbjct: 87 SRTRALLRIADKVEAHIPELAAIESLDNGMPLWYATAAATACADIFRYYAGWCSKVLGTT 146 Query: 127 IQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAI 186 I SD I + LGV I+PWN P + + K A AL GNT+V+KP+E +I Sbjct: 147 IPSDG-STLIYTLREPLGVCGQIIPWNVPVLMASIKFANALCCGNTVVLKPAELACLTSI 205 Query: 187 AFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNIT 246 A+++ E LP GV N++ G G T G LA + V ++ TGS + G++++ A N+ Sbjct: 206 RLAELIQETDLPPGVINVLPGFGPTAGAALAQHLGVDKIAFTGSTAVGKQVVRDATSNLK 265 Query: 247 KVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLG 306 KV LELG KAP +V DADL+ A+ V + NSGQVC+ R++VQ+ I+D+ R+ Sbjct: 266 KVTLELGSKAPNVVFADADLDKAIATAVKTFCGNSGQVCSAGTRLFVQESIHDEVAERVA 325 Query: 307 EAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYP 366 + G+P D +GPLI+A +RV + E GA + GGKA G GY+ Sbjct: 326 SEAATWKAGDPFAA-DTKLGPLISARQRDRVWSYIGAGQESGAALRLGGKAWNGPGYFVE 384 Query: 367 PTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKA 426 PT+ +V+ M I EE FGPVL ++ F +DA+ N++ YGL+++++T++++ A K Sbjct: 385 PTVFDNVKNGMKIAQEEIFGPVLSIIPFKDEDDAVLQGNETTYGLSAAVWTRDVSRAHKV 444 Query: 427 IKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYLQ 478 +K LK G +IN G+++SG G G + Y Q + V ++ Sbjct: 445 VKALKAGRLWINTFGEADPAMAFGGYKQSGWGREFGAESIEAYTQAKSVMVR 496 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: 567 Number of extensions: 21 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: 479 Length of database: 497 Length adjustment: 34 Effective length of query: 445 Effective length of database: 463 Effective search space: 206035 Effective search space used: 206035 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 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