Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_085639722.1 MGEO_RS15320 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_002115805.1:WP_085639722.1 Length = 492 Score = 538 bits (1386), Expect = e-157 Identities = 270/488 (55%), Positives = 355/488 (72%), Gaps = 7/488 (1%) Query: 36 VGGPADLHAD--LLRGDSFVGGRWLPTP--ATFPVYDPASGAKLGTVADCGVPEARAAVR 91 V G DL D +LR +++ G W+ ATF V +PA G + VAD E A+ Sbjct: 5 VTGLKDLLKDPAILRTQAYIAGEWVDADDGATFSVSNPARGDTIAEVADVTRIETALAID 64 Query: 92 AAYDAFSSWKEISVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFF 151 AAY A W + + KER+++LRKW+DLM++N D+LA I+TAE GKP EA+GEILY A F Sbjct: 65 AAYIAQKDWSKWTGKERAAVLRKWFDLMVENADDLATILTAEQGKPHAEARGEILYGASF 124 Query: 152 LEWFSEEARRVYGDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGC 211 +EWF+EEA+R YG+ I +DKR V+KQP+GVA+ ITPWNFP+AMITRKVG ALAAGC Sbjct: 125 VEWFAEEAKRTYGETIPGHQRDKRITVIKQPIGVAASITPWNFPNAMITRKVGPALAAGC 184 Query: 212 TVVVKPAEDTPYSALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFT 271 V +PA +TP SALAL +LA +AGIP GV ++IP SR + ++G+ C +P V K++FT Sbjct: 185 AFVARPAAETPLSALALGELAERAGIPKGVLSIIPSSR--SSDIGKEFCENPKVRKLTFT 242 Query: 272 GSTATGKILLHHAANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCS 331 GST G+ILL AA+ V + SMELGG APFIVFD AN+D AV GA+ SK+RN GQTCVC+ Sbjct: 243 GSTEVGRILLKQAADQVMKCSMELGGNAPFIVFDDANLDAAVEGALISKYRNNGQTCVCA 302 Query: 332 NRFLVQRGIHDSFVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKG 391 NR VQ G++D+F K +A+ +++ VG+G +G GPLINE+AV KVE+HV DA+AKG Sbjct: 303 NRIYVQAGVYDAFAAKLKDAV-EAMPVGDGLSDGVQLGPLINEEAVAKVEEHVEDAIAKG 361 Query: 392 ATVVTGGKRHQSGGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAAD 451 TV++GGKRH GG FF+PT+++ TR+M EETFGP+AP+ FD EE + +AN Sbjct: 362 GTVISGGKRHDLGGTFFQPTIVTGATREMAFAQEETFGPLAPLFNFDTVEEVIDLANDTI 421 Query: 452 VGLAGYFYSQDPAQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDE 511 GLA YFY++D +++ +V E LE GMVGVN GLIS+ PFGGVKQSGLGREGS +G+DE Sbjct: 422 FGLAAYFYARDLSRVTQVQEALEYGMVGVNTGLISTEVAPFGGVKQSGLGREGSHHGMDE 481 Query: 512 YLEVKYVC 519 ++E+KY+C Sbjct: 482 FMEMKYIC 489 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: 680 Number of extensions: 35 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: 492 Length adjustment: 34 Effective length of query: 489 Effective length of database: 458 Effective search space: 223962 Effective search space used: 223962 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