Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_068110959.1 I601_RS14160 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_001653335.1:WP_068110959.1 Length = 471 Score = 369 bits (948), Expect = e-106 Identities = 205/459 (44%), Positives = 279/459 (60%), Gaps = 4/459 (0%) Query: 59 PTPATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEISVKERSSLLRKWYDL 118 P TF V DPA+ +G VAD V + AV A AF+ W + + R+ +L + +L Sbjct: 11 PGTRTFAVLDPANLEPIGEVADHTVEQGVDAVAVASAAFAGWAGTAPRARAEVLSRAREL 70 Query: 119 MIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYGDIIYTSAKDKRGLV 178 M+ ++D LA +I AE+GK +A E+ Y+A F WF+EEA R GD A R LV Sbjct: 71 MVADRDRLADLIVAENGKSRADACAEVTYAAEFFRWFAEEAVRSDGDYSVAPAGGTRTLV 130 Query: 179 LKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYSALALAQLANQAGIP 238 PVGVA+++TPWNFP+AM TRK+ ALAAGCTVV+KPA +TP +ALA+A++ +AG+P Sbjct: 131 THHPVGVAALVTPWNFPAAMATRKIAPALAAGCTVVLKPAAETPLTALAVAEILTEAGVP 190 Query: 239 PGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHAANSVKRVSMELGGL 298 GV NV+P T A V D V K+SFTGST G++LL AA+ V VSMELGG Sbjct: 191 DGVVNVVP--TTDAAGVVGAWLRDDRVRKLSFTGSTGVGRVLLRQAADRVLNVSMELGGN 248 Query: 299 APFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSFVTKFAEAMKKSLRV 358 AP++V A+++ AV GAM +K+RN GQ C +NRF V +FV F A ++LRV Sbjct: 249 APYVVTADADLEAAVQGAMIAKYRNGGQACTAANRFYVHADAAAAFVAGFG-AATEALRV 307 Query: 359 GNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSGGNFFEPTLLSNVTR 418 G G + GPLI+ AV + V AV +GA + SGG FF PT+L++V Sbjct: 308 GPGSDPEAQVGPLISTSAVRALGDLVASAVDEGARIAYQAIA-PSGGGFFPPTVLTDVRP 366 Query: 419 DMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPAQIWRVAEQLEVGMV 478 + E FGPVAP++ + EE+ + N + GLA Y Y+ R+AEQ E GM+ Sbjct: 367 GADILQREIFGPVAPIVVWTDEEDLLRQVNDTEHGLAAYVYAGRLQDALRLAEQFEAGMI 426 Query: 479 GVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKY 517 G+N G++S PFGG KQSGLGREG++ G+ E+ E +Y Sbjct: 427 GINRGIVSDPAAPFGGYKQSGLGREGARAGLAEFQETQY 465 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: 584 Number of extensions: 23 Number of successful extensions: 4 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: 471 Length adjustment: 34 Effective length of query: 489 Effective length of database: 437 Effective search space: 213693 Effective search space used: 213693 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