Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_244906035.1 B9O00_RS05420 NADP-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_900177295.1:WP_244906035.1 Length = 495 Score = 576 bits (1484), Expect = e-169 Identities = 281/489 (57%), Positives = 371/489 (75%), Gaps = 6/489 (1%) Query: 37 GGPADLHADLLRGDSFVGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVRAAY 94 G P L R ++ G+WL AT V +PA+G LG+V G E R A+ AA Sbjct: 11 GSPKLKDGKLFRQQCYIDGQWLDADSGATLEVTNPATGETLGSVPKMGADETRRAIEAAN 70 Query: 95 DAFSSWKEISVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEW 154 A+ +W+ ++ KERS++LR+W++LM+ N+D+L ++T E GKPL EA+GEI Y A F+EW Sbjct: 71 AAWPAWRSLTGKERSNILRRWFELMMANQDDLGLLMTLEQGKPLPEAKGEIAYGASFVEW 130 Query: 155 FSEEARRVYGDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVV 214 F+EEA+RVYGD+I +DKR +VLKQPVGV ITPWNFP+AMITRK G ALAAGCT+V Sbjct: 131 FAEEAKRVYGDVIPGHQRDKRIVVLKQPVGVVGAITPWNFPNAMITRKAGPALAAGCTIV 190 Query: 215 VKPAEDTPYSALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGST 274 +KPA TPYSALAL +LA +AGIP GV+NV+ S + +G L +P+V KISFTGST Sbjct: 191 IKPATATPYSALALCELAERAGIPKGVFNVVTGS---SSAIGGELTGNPIVRKISFTGST 247 Query: 275 ATGKILLHHAANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRF 334 GK+L+ +A +VK++SMELGG APF+VFD A++D AV GAMASK+RNAGQTCVC+NR Sbjct: 248 EVGKVLIKQSAETVKKLSMELGGNAPFLVFDDADLDAAVEGAMASKYRNAGQTCVCANRL 307 Query: 335 LVQRGIHDSFVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATV 394 LVQ G++++F K AE +K+ L+VGNG +EG QGPLI+ A+EKVE+H+ DAVAKGATV Sbjct: 308 LVQDGVYEAFAQKLAEKVKQ-LKVGNGLDEGVVQGPLIDMAAIEKVEEHIADAVAKGATV 366 Query: 395 VTGGKRHQSGGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGL 454 V GGKRH GG+FFEPT+L+ VT +M EETFGPVAP+ +F +EE +A+AN + GL Sbjct: 367 VVGGKRHALGGSFFEPTVLTGVTTEMKVTKEETFGPVAPLFRFGSDEEGIAMANDTEFGL 426 Query: 455 AGYFYSQDPAQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLE 514 A YFY++D +++WRV+E LE G+VG+N G+IS+ PFGGVK+SGLGREGSKYGI+++LE Sbjct: 427 ASYFYARDMSRVWRVSEGLESGIVGINTGIISTEVAPFGGVKESGLGREGSKYGIEDFLE 486 Query: 515 VKYVCYGGL 523 +KY+C GG+ Sbjct: 487 IKYLCMGGV 495 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: 692 Number of extensions: 25 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: 495 Length adjustment: 34 Effective length of query: 489 Effective length of database: 461 Effective search space: 225429 Effective search space used: 225429 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