Align Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized)
to candidate WP_024891002.1 Z164_RS0112375 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q8GAK7 (458 letters) >NCBI__GCF_000559025.1:WP_024891002.1 Length = 462 Score = 362 bits (928), Expect = e-104 Identities = 196/455 (43%), Positives = 277/455 (60%), Gaps = 2/455 (0%) Query: 1 MAIATIDPTTGITLKTFDAHTPEEVENRIARAEAAFRSLQNTSFEERARWMHKAADILES 60 MA AT +P TG TLKTF A TP E++ I RA AAF + + TS ++RA+ + +AA +L + Sbjct: 1 MAFATTNPYTGETLKTFPAATPAEIDAAIERAHAAFLTWRETSLDDRAQVLARAAGLLRA 60 Query: 61 EADEVARLIATEMGKTLTTAKYEALKSATGMRHFADHAQRYLSPETPVPASEVNASNLHV 120 E A ++ EMGK + A+ E A + ++ +H L+P +PA +++ + Sbjct: 61 EPRRFAEILTLEMGKLIGEAEAEVELCAKILDYYVEHGAEGLAPRY-LPAEGFGDTDVQL 119 Query: 121 QFDPLGVVLAVMPWNYPLWQAVRFAAPALMAGNTGLLKHASNVPQCALYLGDLFARGGFP 180 +PLGV+ AV PWN+P +Q +R AP AGN +LKHA+NVPQ AL + LF G P Sbjct: 120 VKEPLGVLFAVEPWNFPFYQVIRITAPQATAGNAIVLKHAANVPQSALAMEQLFRDAGAP 179 Query: 181 EGAFQTLLVEGKDVIPLVDDARIRAVTLTGSVAAGSAIAEAAGRNIKRSVLELGGMDVFI 240 EG L V +D ++ D R+R V LTGS AGSA+A AG+ +K+S LELGG D FI Sbjct: 180 EGLLTNLFVSHEDAERVIADPRVRGVALTGSERAGSAVAALAGKYMKKSTLELGGADAFI 239 Query: 241 VMPSADIEKAAAQAVIARLQNSGQSCIAAKRFYVHEDVYDRFEHLFVTGMAEAVAGDPLD 300 V+ AD+ +AA AV R N+GQ C+++KR V + VYD F + G+A AGDP+D Sbjct: 240 VLSDADVAQAAKWAVFGRHWNAGQVCVSSKRIIVEDAVYDEFLEHYRAGVAALRAGDPMD 299 Query: 301 ESTSFGPLATERGRQDVHELVRDAREKGAAVQCGGEIPEGEGWYYPATVLTGVTEDMRIY 360 +T+ PL++ R + V +A GA + G +PE +G +YP T+LTG+ D Y Sbjct: 300 PATTLAPLSSRSARDGLARQVEEAVAHGAKAETLGTVPE-QGAFYPPTLLTGIAPDNPAY 358 Query: 361 REECFGPVACLYKVSSLQEAIALSNDSDFGLSSSVWTNDETEATEAARSIEAGGVFINGL 420 R E FGPV+ +Y+V++ +EAI L+NDS +GL SV++ D A A +E G V+IN Sbjct: 359 RTEFFGPVSQVYRVANEEEAIRLANDSPYGLGGSVFSQDIARARRVAAKLETGMVYINQP 418 Query: 421 TASFPAVPFGGLKDSGYGRELSAYGIREFVNIKTV 455 T +PFGG+K+SGYG EL G+ EFVN K V Sbjct: 419 TGVKADIPFGGVKNSGYGHELIDLGLNEFVNEKVV 453 Lambda K H 0.317 0.132 0.386 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: 503 Number of extensions: 21 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: 458 Length of database: 462 Length adjustment: 33 Effective length of query: 425 Effective length of database: 429 Effective search space: 182325 Effective search space used: 182325 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: 51 (24.3 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