Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_068010222.1 PsAD2_RS20650 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_001623255.1:WP_068010222.1 Length = 491 Score = 514 bits (1325), Expect = e-150 Identities = 261/480 (54%), Positives = 336/480 (70%), Gaps = 5/480 (1%) Query: 46 LLRGDSFVGGRWLPTPA--TFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 LLR +GG WL + V +PA+G +G V G E A+ AA AF SW ++ Sbjct: 13 LLREACLIGGTWLSGDEQNSIAVTNPATGEIIGRVPRFGRAETAQAIDAASKAFQSWSKM 72 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + ER +L+ W DL+I+N+ +LAK++T E GKPL EA GE+ +A ++ +F+EE +RVY Sbjct: 73 TAVERCNLMHSWADLIIENQTDLAKLLTIEMGKPLAEAAGEVTITANYIRFFAEEGKRVY 132 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 GD+I + + +R V K+P+GV ITPWNFPS+M+ RK+ AAL +GCTVV KPA TPY Sbjct: 133 GDVIPSPWQGRRIFVTKEPIGVVGAITPWNFPSSMLGRKLAAALGSGCTVVAKPASQTPY 192 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SAL L +LA AGIP GV N+I + A E+ + LC + V KI+FTGST GK L Sbjct: 193 SALVLGKLAEDAGIPAGVINIITGT---AAEIADELCENDKVRKITFTGSTPVGKQLASK 249 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 A ++K+VSMELGG APFIVFD+AN+D+AV GA+ASKFRN+GQTCVC+NR VQ G+++ Sbjct: 250 ALANMKKVSMELGGNAPFIVFDTANIDKAVEGAIASKFRNSGQTCVCANRIYVQSGVYEE 309 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A++ LRVGNG + G TQGPLI+ AV KVE+ ++DAV KG TVVTGGKR Sbjct: 310 FSAKLKVAIEVQLRVGNGLKAGVTQGPLIDSNAVAKVEELISDAVEKGGTVVTGGKRDAQ 369 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GG FFEPTLL N T DM EETFGP APV KF+ EEEA+ +AN + GLA YFY+QD Sbjct: 370 GGTFFEPTLLLNATPDMKVAKEETFGPFAPVFKFESEEEAINMANDTEYGLACYFYTQDL 429 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 Q +RV + LE G+VGVNEG+I++ PFGG K SG+G EGSKYGID+Y+ +KY C GGL Sbjct: 430 GQTFRVMDALEYGLVGVNEGVITTEYAPFGGYKDSGMGNEGSKYGIDDYINIKYSCIGGL 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: 669 Number of extensions: 26 Number of successful extensions: 2 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