Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_240484289.1 AU252_RS01005 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_001484605.1:WP_240484289.1 Length = 506 Score = 422 bits (1085), Expect = e-122 Identities = 229/468 (48%), Positives = 299/468 (63%), Gaps = 5/468 (1%) Query: 53 VGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEISVKERSS 110 +GG+W+ TF V+DPA+G L T+A +A AA+ AA +SW + +ER+ Sbjct: 34 IGGQWVEASDGGTFDVHDPATGEVLATLASATSEDAVAALDAADKVQASWARTAPRERAE 93 Query: 111 LLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYGDIIYTS 170 +LR+ ++L+ + ++ A ++T E GKPL EA+GE+ Y A FL WFSEE R YG + T Sbjct: 94 ILRRAFELVTERAEDFALLMTLEMGKPLAEARGEVTYGAEFLRWFSEETVRDYGRYLTTP 153 Query: 171 AKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYSALALAQ 230 + LV +PVG +ITPWNFP AM TRKV A+AAGCT+V+KPA+ TP +A AQ Sbjct: 154 EGKNKILVQHKPVGPCLLITPWNFPLAMATRKVAPAIAAGCTMVLKPAKLTPLTAQYFAQ 213 Query: 231 LANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHAANSVKR 290 AG+P GV NV+ S + A + L D + K+SFTGST GK L+ AA +V R Sbjct: 214 TMLDAGLPAGVLNVV--SSSSASGISGPLMKDSRLRKVSFTGSTPVGKRLIADAAQNVLR 271 Query: 291 VSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSFVTKFAE 350 SMELGG APFIVF+ A++D+AV GAMA+K RN G+ C +NRFLVQ + F +FA Sbjct: 272 TSMELGGNAPFIVFEDADLDKAVEGAMAAKMRNMGEACTAANRFLVQESVAAEFTRRFAA 331 Query: 351 AMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSGGNFFEP 410 AM SL G G E GT GPLI+ A + V V+ AV GAT VTGG G F+ P Sbjct: 332 AM-GSLATGRGTEPGTQVGPLIDAGARDDVHALVSAAVEAGATAVTGGSPLDGPGYFYPP 390 Query: 411 TLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPAQIWRVA 470 T+L NV D + +E FGPVAPV F EE+A+ +ANA++ GLA Y YS+D ++ RVA Sbjct: 391 TVLGNVPNDAAILRQEIFGPVAPVTTFSTEEDAIRLANASEYGLASYIYSRDFNRLLRVA 450 Query: 471 EQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYV 518 EQ+E GMVG N G+IS+ PFGGVKQSGLGREG GI EY +Y+ Sbjct: 451 EQIEFGMVGFNAGVISNAAAPFGGVKQSGLGREGGSEGIAEYTTTQYI 498 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: 648 Number of extensions: 26 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: 506 Length adjustment: 35 Effective length of query: 488 Effective length of database: 471 Effective search space: 229848 Effective search space used: 229848 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