Align Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized)
to candidate WP_101589014.1 BJEO58_RS08335 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q8GAK7 (458 letters) >NCBI__GCF_900169175.1:WP_101589014.1 Length = 457 Score = 359 bits (921), Expect = e-103 Identities = 198/451 (43%), Positives = 267/451 (59%), Gaps = 3/451 (0%) Query: 5 TIDPTTGITLKTFDAHTPEEVENRIARAEAAFRSLQNTSFEERARWMHKAADILESEADE 64 T P G LK F A E+ + IA + AAF++ + T E+R + +AAD++E DE Sbjct: 7 TTGPANGEMLKEFPAAADHEIADAIAASHAAFQTWRTTPVEKRTEPIRRAADLMEERIDE 66 Query: 65 VARLIATEMGKTLTTAKYEALKSATGMRHFADHAQRYLSPETPVPASEVNASNLHVQFDP 124 ++RL+ EMGK A+ E A +R++AD +L+ E P S V+ +P Sbjct: 67 LSRLLTLEMGKLTAEARAEVELCAKILRYYADEGPGHLADERRTPDSGGTGV---VKKEP 123 Query: 125 LGVVLAVMPWNYPLWQAVRFAAPALMAGNTGLLKHASNVPQCALYLGDLFARGGFPEGAF 184 G ++ VMPWN+P +Q VR AAP L+AGNT LLKHA N PQ A+ L + G P+ + Sbjct: 124 KGPLIGVMPWNFPYYQVVRLAAPNLIAGNTILLKHAPNCPQSAVAFAALMSDAGLPDDCY 183 Query: 185 QTLLVEGKDVIPLVDDARIRAVTLTGSVAAGSAIAEAAGRNIKRSVLELGGMDVFIVMPS 244 L + + ++ D R+ +LTGS AAGSA+A AG N+ + +LELGG D FIV+ S Sbjct: 184 INLFADTDQIQTIIADERVAGASLTGSEAAGSAVAAGAGENLTKVILELGGSDPFIVLDS 243 Query: 245 ADIEKAAAQAVIARLQNSGQSCIAAKRFYVHEDVYDRFEHLFVTGMAEAVAGDPLDESTS 304 D+++ + AV R+ N+GQSCIA+KR V ED Y+ F F T MA GDP D T+ Sbjct: 244 DDLDETVSTAVAGRMANAGQSCIASKRLIVVEDHYEEFVEKFTTAMAGFTPGDPADPDTT 303 Query: 305 FGPLATERGRQDVHELVRDAREKGAAVQCGGEIPEGEGWYYPATVLTGVTEDMRIYREEC 364 PL++E+ D+ E V DA E+GA VQ GG + G Y TVLTGV MR Y EE Sbjct: 304 LAPLSSEQAAADLMEQVHDAVEQGATVQIGGGRVDRPGAYVQPTVLTGVIPSMRAYSEEL 363 Query: 365 FGPVACLYKVSSLQEAIALSNDSDFGLSSSVWTNDETEATEAARSIEAGGVFINGLTASF 424 FGPVA +Y+V+ +EAI L+NDS FGL SV + D A A I++ V+IN T + Sbjct: 364 FGPVAVIYRVADEEEAIHLANDSSFGLGGSVMSADPARARRVADRIDSAMVWINAATWTE 423 Query: 425 PAVPFGGLKDSGYGRELSAYGIREFVNIKTV 455 P +PFGG K SG GREL A GI EFVN K + Sbjct: 424 PDLPFGGTKRSGIGRELGAEGILEFVNKKLI 454 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: 478 Number of extensions: 13 Number of successful extensions: 2 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: 457 Length adjustment: 33 Effective length of query: 425 Effective length of database: 424 Effective search space: 180200 Effective search space used: 180200 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