Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_094508970.1 CEV31_RS17495 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_002252445.1:WP_094508970.1 Length = 482 Score = 510 bits (1313), Expect = e-149 Identities = 261/480 (54%), Positives = 341/480 (71%), Gaps = 6/480 (1%) Query: 46 LLRGDSFVGGRW--LPTPATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 L R +GG W + AT V +PAS LGT+ D G+ E RAA+ AA AF WK+ Sbjct: 7 LFRQQGLIGGVWQDAASTATLDVTNPASLRALGTIPDMGITETRAAIDAAAAAFKPWKKK 66 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + ER++LL +W+ LMI+++ +LA ++T E GKPL EA GEI Y A F++WF+EEARR+ Sbjct: 67 THAERAALLERWFALMIEHEQDLALLLTLEQGKPLPEALGEIRYGASFVKWFAEEARRID 126 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 G I + D+R LVLK+ VGV +IITPWNFP+AMITRKV ALAAGCTVV+KP+E TP+ Sbjct: 127 GGSIPSPTADRRILVLKEAVGVCAIITPWNFPNAMITRKVAPALAAGCTVVIKPSEFTPF 186 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SALAL LA +AGIP GV N++ E+G L + V KISFTGST G +L+ Sbjct: 187 SALALGALAERAGIPAGVINIV---TGMPSEIGNELMANETVRKISFTGSTRVGSLLMKG 243 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 AA+S+KR+S+ELGG APFIVFD A++DQAV GA+ASKFRN GQTCVCSNR LVQ GI+D+ Sbjct: 244 AADSIKRLSLELGGNAPFIVFDDADLDQAVEGAIASKFRNGGQTCVCSNRILVQAGIYDA 303 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K + + + ++VG G EEG GP+IN A+EK+E+HV+DA+ +GA ++ + Sbjct: 304 FAAKLSSRVAQ-MKVGIGTEEGVVIGPMINHAAIEKIERHVSDALGRGAKILAQSETMPE 362 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 G + P +L + T DML +EETFGPVAP+ +F+ EEEA+ IAN GLA YF++++ Sbjct: 363 GRQYARPIVLGDATTDMLLASEETFGPVAPLFRFETEEEAIEIANGTPFGLAAYFFTENL 422 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 + WRVAE LE GM+G+N G IS+ PFGGVKQSGLGREGSK GI+EYLE+K + GGL Sbjct: 423 KRSWRVAEALEFGMIGLNTGAISTEVAPFGGVKQSGLGREGSKLGIEEYLEIKTLHVGGL 482 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: 618 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: 482 Length adjustment: 34 Effective length of query: 489 Effective length of database: 448 Effective search space: 219072 Effective search space used: 219072 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