Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_043531966.1 JH15_RS15380 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000759345.1:WP_043531966.1 Length = 483 Score = 555 bits (1429), Expect = e-162 Identities = 274/480 (57%), Positives = 357/480 (74%), Gaps = 6/480 (1%) Query: 46 LLRGDSFVGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 L R ++ G W AT V +PA+ +LGTV E AA+ AA A WK Sbjct: 8 LFRQHCYIDGCWADAEDKATIEVTNPATNDRLGTVPKLSKDEVSAAIDAADRALPLWKAK 67 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + KER+S+LR+W+DL ++++++LA+I+T E GKPL+EA+GEI Y A F+EWF EEA+RVY Sbjct: 68 TAKERASILRRWFDLCMEHQEDLAQILTLEQGKPLQEARGEIAYGASFIEWFGEEAKRVY 127 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 GD+I AKD+R +V K+PVGV + ITPWNFP+AMITRK AA+AAGCTV+VKPA TPY Sbjct: 128 GDVIPAHAKDRRIVVTKEPVGVVAAITPWNFPNAMITRKAAAAMAAGCTVIVKPASSTPY 187 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SALALA+LA +AG+P GV NV+ S A VG L +P V K+SFTGST GKILL Sbjct: 188 SALALAELAERAGVPRGVLNVVTGS---ASVVGGELTANPRVRKLSFTGSTEVGKILLGE 244 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 A +VK+VSMELGG APFI+F+ A++DQAVAG MASKFRN GQTCVC+NR V I+D Sbjct: 245 CAKTVKKVSMELGGNAPFIIFEDADLDQAVAGVMASKFRNTGQTCVCANRIFVHDKIYDD 304 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F + A A+ +VG+G E+G + GPLIN AVEKVE+H+ DA+AKGA+V GGKRH+ Sbjct: 305 FTDRLATAVSAQ-KVGSGLEDGVSLGPLINPAAVEKVEQHIEDAIAKGASVYLGGKRHEL 363 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GNFF+PT+L+NV+ D + + +ETFGPVAP+++F E++ + AN +GLA YFY++D Sbjct: 364 QGNFFQPTILTNVSSDSMLMHDETFGPVAPLLRFTDEDDVIRQANDTTLGLASYFYTRDV 423 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 ++WRVAE LE G+VG+NEG+ISS PFGGVK+SG+GREGSKYGID+Y+E+KY+C GGL Sbjct: 424 GRVWRVAEALECGIVGINEGIISSELAPFGGVKESGIGREGSKYGIDDYIEIKYLCMGGL 483 Lambda K H 0.318 0.135 0.400 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: 661 Number of extensions: 17 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: 523 Length of database: 483 Length adjustment: 34 Effective length of query: 489 Effective length of database: 449 Effective search space: 219561 Effective search space used: 219561 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