Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_085635072.1 MGEO_RS02345 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_002115805.1:WP_085635072.1 Length = 491 Score = 514 bits (1324), Expect = e-150 Identities = 255/475 (53%), Positives = 345/475 (72%), Gaps = 4/475 (0%) Query: 46 LLRGDSFVGGRWLP-TPATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEIS 104 LL ++V G W+ TF V +PA G K+ VAD + A+ AA A W + + Sbjct: 17 LLETRAYVNGAWIDGDDGTFAVDNPARGDKIADVADLSRAQVADAITAAEKAQKEWAKWT 76 Query: 105 VKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYG 164 KER+++LRKW+DLM++N+D+LA I+TAE GKPL EA+GEI Y A F+E+F+EEA+RVYG Sbjct: 77 GKERAAVLRKWFDLMMENQDDLATILTAEQGKPLAEAKGEIAYGASFIEFFAEEAKRVYG 136 Query: 165 DIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYS 224 + I +DKR +V+KQP+GV ITPWNFP+AMITRK G AL+AGC+ V +PA +TP S Sbjct: 137 ETIPGHQRDKRIMVMKQPIGVVGSITPWNFPNAMITRKAGPALSAGCSFVARPAAETPLS 196 Query: 225 ALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHA 284 A+ L LA +AGIP GV N++P S A EVG+ +C +P+V KI+FTGST G+ILL A Sbjct: 197 AIVLGVLAERAGIPAGVLNIVPSS--SASEVGKEMCENPIVRKITFTGSTEVGRILLRQA 254 Query: 285 ANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSF 344 A+ V + SMELGG APFIVFD A++D AV GA+ KFRN GQTCVC+NR VQ G++D+F Sbjct: 255 ADQVMKCSMELGGNAPFIVFDDADLDAAVDGAIMCKFRNNGQTCVCANRIYVQAGVYDAF 314 Query: 345 VTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSG 404 K + + K ++VG+G E GT GPLIN +A++KV +H+ DA +KGA V+ G + + Sbjct: 315 AQKLKDKVSK-MKVGDGLEAGTDLGPLINPEALDKVREHIADAKSKGAQVILGDESGSND 373 Query: 405 GNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPA 464 GNF PT+++ TRDM TEETFGP+AP+ KF+ E++ + +AN GLA YFY++D + Sbjct: 374 GNFIAPTIVTGATRDMAFSTEETFGPLAPLFKFETEDDVIELANDTIFGLASYFYAKDLS 433 Query: 465 QIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVC 519 ++++VAE LE G+VGVN G+IS+ PFGGVKQSGLGREGS +GI+E+LE+KYVC Sbjct: 434 RVYKVAEALEYGIVGVNTGIISTEVAPFGGVKQSGLGREGSHHGIEEFLEMKYVC 488 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: 592 Number of extensions: 21 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: 491 Length adjustment: 34 Effective length of query: 489 Effective length of database: 457 Effective search space: 223473 Effective search space used: 223473 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