Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_050463371.1 AKL27_RS13585 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_001189915.1:WP_050463371.1 Length = 488 Score = 539 bits (1388), Expect = e-157 Identities = 270/480 (56%), Positives = 357/480 (74%), Gaps = 6/480 (1%) Query: 46 LLRGDSFVGGRWLPTPA--TFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 LLR +GG W + F V DPASGA + +V G E R A+ AA A +W+ Sbjct: 13 LLRQQCHIGGDWQDAASGERFDVTDPASGAVIASVPLAGADETRQAIAAAEQALPAWRAK 72 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + ER+ +LR W++L++ ++D+LA+I+T E GKPL EA+GEI Y+A ++EWF+EE +R Y Sbjct: 73 TAAERARILRNWFNLLLTHQDDLARIMTLEQGKPLAEAKGEIAYAAAYIEWFAEEGKRAY 132 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 G++I + D+R LV+KQPVGV + ITPWNFP+AMITRKV ALAAGCT+V+KPAE TP Sbjct: 133 GEVIPSPFADRRLLVVKQPVGVCAAITPWNFPAAMITRKVAPALAAGCTMVLKPAELTPL 192 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SALALA+LA +AGIP GV+NV+ + +G L + P+V K+SFTGST G++L+ Sbjct: 193 SALALAELATRAGIPAGVFNVV---TGNPRAIGGELTSSPIVRKLSFTGSTEVGRLLMAQ 249 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 A ++K++S+ELGG APFIVFD A++D AVAGA+ASK+RN GQTCVCSNRFLVQ GI+D+ Sbjct: 250 CAPTIKKLSLELGGNAPFIVFDDADLDAAVAGAIASKYRNTGQTCVCSNRFLVQAGIYDA 309 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A A+ +L+VG GFE TQGPLINE AV KVE V+DA+AKGA VV GGKRH Sbjct: 310 FAQKLAVAV-AALKVGQGFEADVTQGPLINEAAVSKVEHLVSDALAKGAQVVAGGKRHAR 368 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GG ++EPT+++ +T DM +E FGPVA + +F+ E +AVA+AN + GLA YFY++D Sbjct: 369 GGLWYEPTVMTGLTPDMALARQEIFGPVAGLFRFEDEAQAVAMANDTEFGLAAYFYTRDN 428 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 A+IWRV+E LE GMVG+N GLIS+ PFGGVK SGLGREGS++G+D+YLE+KY+ GGL Sbjct: 429 ARIWRVSEALEYGMVGINTGLISTEVAPFGGVKNSGLGREGSRHGLDDYLELKYLAMGGL 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: 659 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: 488 Length adjustment: 34 Effective length of query: 489 Effective length of database: 454 Effective search space: 222006 Effective search space used: 222006 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