Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_052591776.1 VV02_RS12055 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_001190945.1:WP_052591776.1 Length = 486 Score = 287 bits (735), Expect = 5e-82 Identities = 160/474 (33%), Positives = 263/474 (55%), Gaps = 2/474 (0%) Query: 5 VQHPMYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALP 64 V+ ++I G++ G A ++V NPAT ++ + DG +D A+ AA AQ +W P Sbjct: 12 VKKQLFIAGEWRDAEGGATLEVDNPATGEALTHVADGSVKDGDAALAAAAAAQADWAKTP 71 Query: 65 AIERASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEG 124 +R LR + ER +++ L+ E GK + EVA+ +++ + +E A R G Sbjct: 72 PRDRGELLRSAYEMLVERTEDLATLMTLEMGKPLAESRGEVAYGSEFFRWFSEEAVRISG 131 Query: 125 EIIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNN 184 + ++ K+ +G T I PWNFP + RK+ PA+ G T+V+KP+ TP Sbjct: 132 RWSTAPNGATRLVTMKQPVGPTLMITPWNFPLAMGTRKIGPAIAAGCTMVVKPAAETPLT 191 Query: 185 AIAFAKIVDEIGLPRGVFNLV-LGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAK 243 + A+I++E+GLP+GV N++ V + L +P+ ++ TGS G+K++ +A+ Sbjct: 192 MLLLAQILEEVGLPKGVLNVITTSTSGQVMEPLIRDPRSRKLTFTGSTPIGQKLIEQSAE 251 Query: 244 NITKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVN 303 + +V +ELGG AP +V +DADL+ AV+ + +++ N G+ C A R V + D+F Sbjct: 252 QLLRVSMELGGNAPFLVFEDADLDAAVEGAMLAKMRNIGEACTAANRFLVHADVADEFSR 311 Query: 304 RLGEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGY 363 RL E M A+ G+ + +D +GPLINA A+++V+ V A GARV GG+ V +G+ Sbjct: 312 RLAERMGALTVGDGMD-DDTKVGPLINAKAVDKVKALVEDAKGRGARVVTGGETVGDRGF 370 Query: 364 YYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVA 423 +Y PT+L DV E + EE FGPV + F DAI AN ++YGL + +T++ + A Sbjct: 371 FYAPTVLTDVTGEADMAREEIFGPVAGIQTFTDEADAIERANSTEYGLVAYFFTKDFSRA 430 Query: 424 MKAIKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYL 477 ++ + L++G +N+ G + SG G G G+ EYL+T+ V L Sbjct: 431 IRVSEALEYGMVGVNQGIVSNPAAPFGGVKASGFGREGGFEGIDEYLETKYVGL 484 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: 540 Number of extensions: 28 Number of successful extensions: 4 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