Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_053938969.1 WG78_RS16670 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_001294205.1:WP_053938969.1 Length = 466 Score = 535 bits (1377), Expect = e-156 Identities = 268/465 (57%), Positives = 347/465 (74%), Gaps = 6/465 (1%) Query: 44 ADLLRGDSFVGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWK 101 + LLR FV G W+ T PV +PA+G + + G E R A+ AA A+ +W+ Sbjct: 6 SSLLRQQCFVNGAWIDADNQETVPVNNPATGEIIAHIPKLGKAETRRAIEAAQAAWPAWR 65 Query: 102 EISVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARR 161 + KERS +LRKW DLM+ N D+LA I+T+E GKPL EA+GEI Y+A ++EWF+EEARR Sbjct: 66 SKTAKERSQILRKWNDLMLANVDDLALILTSEQGKPLAEARGEITYAASYIEWFAEEARR 125 Query: 162 VYGDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDT 221 + GDII + D+R LVLKQP+GV + ITPWNFP+AMITRKVG ALAAGC +V+KPA T Sbjct: 126 IEGDIIAPPSNDRRILVLKQPIGVTAAITPWNFPAAMITRKVGPALAAGCPMVLKPATQT 185 Query: 222 PYSALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILL 281 P SALALA LA +AG+P G++NV+ S T E+G L P+V KI+FTGST G L+ Sbjct: 186 PLSALALAVLAERAGVPAGIFNVLTGSST---EIGGELTASPIVRKITFTGSTEVGAKLI 242 Query: 282 HHAANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIH 341 +A ++K++SMELGG APFIVFD A++D AV GA+ SK+RN+GQTCVC+NR LVQ G++ Sbjct: 243 EQSAPTIKKMSMELGGNAPFIVFDDADLDAAVQGAIGSKYRNSGQTCVCANRLLVQAGVY 302 Query: 342 DSFVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRH 401 D+F K A+A+ +L+VGNG ++G TQGPLI++KA+ K+E+H+ DA KGA V+TGGKRH Sbjct: 303 DAFAQKLADAV-NALKVGNGVDDGVTQGPLIDDKAIAKIEEHIADATGKGAQVLTGGKRH 361 Query: 402 QSGGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQ 461 GG FFEPT+L+ VT M EETFGP+AP+ KF+ EEEA+A+AN + GLA YFY++ Sbjct: 362 ALGGTFFEPTILTGVTPAMKVAREETFGPLAPLFKFETEEEAIAMANDTEFGLASYFYTR 421 Query: 462 DPAQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSK 506 D A+I+RVAE LE GMVG+N GLISS PFGGVKQSGLGREGS+ Sbjct: 422 DLARIFRVAEGLEYGMVGINAGLISSEVAPFGGVKQSGLGREGSR 466 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: 627 Number of extensions: 20 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: 466 Length adjustment: 34 Effective length of query: 489 Effective length of database: 432 Effective search space: 211248 Effective search space used: 211248 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