Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_110804869.1 C8J30_RS06315 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_003217355.1:WP_110804869.1 Length = 492 Score = 510 bits (1314), Expect = e-149 Identities = 258/476 (54%), Positives = 337/476 (70%), Gaps = 5/476 (1%) Query: 46 LLRGDSFVGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 LL + V G W+ TF V +PA G + TV D + A++AA A W Sbjct: 17 LLCTKALVAGEWVDAEDGKTFAVMNPARGDVICTVPDLTRADTARAIKAAEVAMKDWAAR 76 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + KER++++RKW++LM+ N+++LA I+TAE GKPL EA+GEI Y A F+EWF EEA+R+Y Sbjct: 77 TGKERAAVMRKWFELMMANQEDLALILTAEMGKPLAEARGEIAYGASFIEWFGEEAKRIY 136 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 G+ I +DKR VLKQP+GV ITPWNFP+AMI RK G A+A GC V +PA +TP Sbjct: 137 GETIPGHMRDKRITVLKQPIGVVGSITPWNFPNAMIARKAGPAIAVGCGFVCRPASETPL 196 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SALA+ L +AG+P G+ +VI SR A ++G+ C + V K++FTGST G+ILL Sbjct: 197 SALAMGLLGERAGLPKGILSVITSSR--ASDIGKEFCENHAVRKLTFTGSTEVGRILLRQ 254 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 AA+ V + SMELGG APFIVFD A++D AV GAM SKFRN GQTCVC+NR VQ G++D+ Sbjct: 255 AADQVMKCSMELGGNAPFIVFDDADLDAAVEGAMMSKFRNNGQTCVCANRIYVQAGVYDT 314 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A A++K L VG+G ++G T GPLI+ AVEKVE+H+ D VA G T+VTGG RH+ Sbjct: 315 FAEKLAAAVRK-LNVGDGLKDGVTTGPLISADAVEKVEEHIADVVAGGGTIVTGGARHEL 373 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GG FF+PT+++ VT+ M TEETFGPVAP+ KF+ E E + ANA GLA YFY++D Sbjct: 374 GGTFFQPTVVTGVTQAMKVATEETFGPVAPLFKFETEAEVIEKANATIFGLASYFYARDV 433 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVC 519 +I RV E LE G+VGVN G+IS+ PFGGVKQSGLGREGS +G+++YLE+KYVC Sbjct: 434 GRITRVQEGLEYGIVGVNTGIISTEVAPFGGVKQSGLGREGSHHGVEDYLELKYVC 489 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: 648 Number of extensions: 27 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: 492 Length adjustment: 34 Effective length of query: 489 Effective length of database: 458 Effective search space: 223962 Effective search space used: 223962 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