Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_050464411.1 AKL27_RS18955 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_001189915.1:WP_050464411.1 Length = 484 Score = 531 bits (1368), Expect = e-155 Identities = 259/480 (53%), Positives = 349/480 (72%), Gaps = 6/480 (1%) Query: 46 LLRGDSFVGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 L R ++ G W A V +PA+G LGT+ G E A+ AA A+ W++ Sbjct: 9 LFRQQCYIDGVWTDADDGAAVAVNNPATGDILGTIPKMGRTETARAIAAANVAWGEWRKK 68 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + KER+ ++R+W+DLM+ N D+LA I+T+E GKPL E++GE+ Y+A +LEWF+EE +R Y Sbjct: 69 TAKERALIMRRWFDLMLANADDLALIMTSEQGKPLAESKGEVTYAASYLEWFAEEGKRAY 128 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 GD I ++ + R +V+K+P+GV + ITPWNFP+AMITRKVGAAL AGC +VVKPA TP+ Sbjct: 129 GDTIPRASGETRIVVIKEPIGVCAAITPWNFPAAMITRKVGAALGAGCPIVVKPATQTPF 188 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SALALA LA +AG+P GV++V+ + A +G + +P V K+SFTGST G+ L+ Sbjct: 189 SALALAVLAEEAGVPKGVFSVVTGA---AAAIGAEMTENPTVRKLSFTGSTEVGRKLMEQ 245 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 +A ++K+VSMELGG APFIVFD A++D AV GA+ASKFRN GQTCVC+NR VQ G++D+ Sbjct: 246 SAATIKKVSMELGGNAPFIVFDDADLDAAVVGAIASKFRNTGQTCVCANRIYVQDGVYDA 305 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A++K L+VG+G ++ TQGPLI+ AV K+E+HV D +AKG +VTGGK H Sbjct: 306 FAAKLVAAVQK-LKVGSGIDKDVTQGPLIDGNAVRKIEEHVADIIAKGGKIVTGGKPHAL 364 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 G FFEPT+ N T+DML EETFGP+AP+ +F K+EE VA AN + GLA YFY++D Sbjct: 365 GQTFFEPTVALNATQDMLVAKEETFGPLAPLFRFHKDEEVVAFANDTEFGLASYFYTRDI 424 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 ++WRVAE LE GMVG+N G+IS+ PFGGVKQSGLGREGS+YG+D+YL KY+C GG+ Sbjct: 425 GRVWRVAEGLEYGMVGINTGIISNEMAPFGGVKQSGLGREGSRYGLDDYLVTKYLCIGGI 484 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: 18 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: 484 Length adjustment: 34 Effective length of query: 489 Effective length of database: 450 Effective search space: 220050 Effective search space used: 220050 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