Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_012759625.1 RLEG_RS21595 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000023185.1:WP_012759625.1 Length = 493 Score = 535 bits (1378), Expect = e-156 Identities = 267/480 (55%), Positives = 344/480 (71%), Gaps = 5/480 (1%) Query: 46 LLRGDSFVGGRWLPTPAT--FPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 LLR ++ G W AT F V +PA+G L ++ D G E R A+ AA+ A W Sbjct: 17 LLRDAGYIDGVWTSGDATRTFDVLNPATGELLASLPDMGAAETRTAIDAAHAAQPGWAAR 76 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 KERS++LRKW+DLM+ N DELA I+TAE GKP EA+GEILY+A ++EW++EEA+R+Y Sbjct: 77 PAKERSTILRKWFDLMVANADELAAILTAEMGKPFPEARGEILYAAAYIEWYAEEAKRIY 136 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 G+ I + DKR +V++QPVGV ITPWNFP+AMITRK+ ALA GCTVV KPAE TP Sbjct: 137 GETIPAPSDDKRMIVIRQPVGVVGTITPWNFPAAMITRKIAPALAVGCTVVSKPAEQTPL 196 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 +A+ALA LA QAGIP GV+NVI +G LC + V KISFTGST G+IL+ Sbjct: 197 TAIALAVLAEQAGIPAGVFNVI--VGVDGPAIGRELCGNEKVRKISFTGSTEVGRILMRQ 254 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 A+ +K+VS+ELGG APFIVFD A++D AV GA+ASK+RNAGQTCVC+NR VQ ++D+ Sbjct: 255 CADQIKKVSLELGGNAPFIVFDDADLDAAVEGAIASKYRNAGQTCVCANRLYVQSNVYDA 314 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A A + VG+GF+ G GPLI+E+ + KVE HV+DA+AKGA V+TGGKR Sbjct: 315 FAAKLA-AKVAEMSVGDGFKPGVVIGPLIDEQGLAKVEDHVSDALAKGAKVLTGGKRIDG 373 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 G FF PT+L+ V R M EETFGPVAP+ +F+ E+ +A AN + GLA YFY+ D Sbjct: 374 AGTFFTPTVLTGVARGMKVAREETFGPVAPLFRFETVEDVIAQANDTEFGLAAYFYAGDL 433 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 ++WRVAE LE GM+G+N GL+SS PFGG+KQSGLGREGS++G D+YLE+KY+C GG+ Sbjct: 434 KKVWRVAEALEYGMIGINTGLMSSETAPFGGIKQSGLGREGSRHGADDYLEMKYLCIGGV 493 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: 658 Number of extensions: 23 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: 493 Length adjustment: 34 Effective length of query: 489 Effective length of database: 459 Effective search space: 224451 Effective search space used: 224451 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