Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_043532311.1 JH15_RS16505 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000759345.1:WP_043532311.1 Length = 487 Score = 516 bits (1329), Expect = e-151 Identities = 258/476 (54%), Positives = 338/476 (71%), Gaps = 5/476 (1%) Query: 46 LLRGDSFVGGRWLPTPA--TFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 L R +++ G W+ + V++PA+G +G V G E A+ AA AF +W+ Sbjct: 9 LFRPFAYIDGSWVAADSGEQIDVFNPANGEVIGRVPRLGRAETERAITAADAAFPAWRAH 68 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + +ER+ +L KW+DLM ++++ELA I+T E GKPLKEA GEI Y+A FL WF+EEARR+Y Sbjct: 69 TAQERADILMKWHDLMHEHQEELATIMTLEQGKPLKEAAGEIAYAASFLRWFAEEARRMY 128 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 G+ I + ++R ++ KQPVGV ITPWNFP+AMITRKVGAALAAGC +VVKPA TP+ Sbjct: 129 GETIPAAKPNQRIVITKQPVGVVGAITPWNFPAAMITRKVGAALAAGCPIVVKPASQTPF 188 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SA ALA LA +AG+P GV+NV+ S A+E+ L P V KI+FTGST G+ L+ Sbjct: 189 SATALALLAERAGVPRGVFNVVTGS---AREIAAALTESPEVRKITFTGSTEVGRQLMSQ 245 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 A+ ++++S+ELGG APFIVF+ A++D AV GAMA+KFRN GQTCVC+NRFLVQ + ++ Sbjct: 246 ASQHIQKISLELGGNAPFIVFEDADLDAAVDGAMAAKFRNGGQTCVCTNRFLVQSSVVNA 305 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A AM LRVG+G ++ GPLI+ VEKV HV+DAV KGA ++ GG H Sbjct: 306 FCEKLAVAMNSELRVGDGLKDDVNIGPLIDADGVEKVSAHVHDAVDKGAELLLGGNPHPL 365 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GGNFF PTL++ DML EETFGP+A V FD EE+AVA+AN GLA YFYS+D Sbjct: 366 GGNFFTPTLVNGANADMLVAQEETFGPLAAVFPFDDEEDAVAMANDTQFGLASYFYSRDL 425 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVC 519 A++WRVAE LE GMVG+N GLIS+ PFGGVK SGLGREG + G++E++E KY+C Sbjct: 426 ARVWRVAESLEYGMVGINTGLISNAAAPFGGVKASGLGREGGRQGLEEFVETKYLC 481 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: 642 Number of extensions: 23 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: 487 Length adjustment: 34 Effective length of query: 489 Effective length of database: 453 Effective search space: 221517 Effective search space used: 221517 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