Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_023434135.1 N177_RS19425 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000496075.1:WP_023434135.1 Length = 489 Score = 546 bits (1408), Expect = e-160 Identities = 273/480 (56%), Positives = 366/480 (76%), Gaps = 5/480 (1%) Query: 44 ADLLRGDSFVGGRWLPTPATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 A LL+ +V GRW+ V +PA+G L +V G EAR A+ AA AF W + Sbjct: 13 ASLLKSQCYVNGRWVGE-GEIAVTNPATGETLASVPRFGGAEAREAIEAAEKAFKPWAKK 71 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + KERS +LR+WY+LM++NK++LA I+T+E GKPL E++GEI Y+A F+E+F+EEA+R+Y Sbjct: 72 TAKERSKILRRWYELMMENKEDLAFIMTSEQGKPLTESRGEIDYAANFVEFFAEEAKRIY 131 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 GD I + D R +V KQP+GV ITPWNFP+AMITRK G ALAAGCT+VVKPA +TP Sbjct: 132 GDTIPSHKADARIVVGKQPIGVTCAITPWNFPAAMITRKAGPALAAGCTMVVKPATETPL 191 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 +ALALA+LA++AGIP GV++VI K+ E+G + ++P+V I+FTGST GK L+ Sbjct: 192 TALALAELAHRAGIPEGVFSVIT---GKSSEIGAEMTSNPIVKLITFTGSTEVGKKLMEQ 248 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 +A++VK+V++ELGG APF+VFD A++D AV GA+ASKFRN GQTCVC+NR VQ G++++ Sbjct: 249 SASTVKKVALELGGNAPFLVFDDADLDAAVQGAIASKFRNMGQTCVCANRIYVQSGVYEA 308 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K AEA+KK L+VG+G +E QGPLINE AV+KVE+H++DA +KGA VV GGKR Sbjct: 309 FAGKLAEAVKK-LKVGDGAQEDVQQGPLINEDAVKKVEEHISDATSKGAKVVLGGKRSDL 367 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 G +FF+PT+L++VT +M+ EETFGPVAP+ +F+ EEEA+ +ANA GLA YFYS+D Sbjct: 368 GHSFFQPTVLTDVTPEMVVTREETFGPVAPLFRFETEEEAIELANATQFGLASYFYSRDI 427 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 + WRVAE LE G+VG+NEGLIS+ PFGGVK+SG+GREGS YG+DE++EVKY+ GGL Sbjct: 428 GRCWRVAEALEYGIVGINEGLISTEVAPFGGVKESGIGREGSHYGMDEFVEVKYMLMGGL 487 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: 652 Number of extensions: 19 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: 489 Length adjustment: 34 Effective length of query: 489 Effective length of database: 455 Effective search space: 222495 Effective search space used: 222495 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