Align Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized)
to candidate WP_076479348.1 BW971_RS10750 NADP-dependent succinic semialdehyde dehydrogenase
Query= SwissProt::Q8GAK7 (458 letters) >NCBI__GCF_900156495.1:WP_076479348.1 Length = 457 Score = 508 bits (1309), Expect = e-148 Identities = 255/456 (55%), Positives = 319/456 (69%), Gaps = 1/456 (0%) Query: 1 MAIATIDPTTGITLKTFDAHTPEEVENRIARAEAAFRSLQNTSFEERARWMHKAADILES 60 MAIA+I+P TG L+ FDA T EVE+R+A A + T +RA + AADIL++ Sbjct: 1 MAIASINPATGELLEEFDALTDAEVESRLATAARVAVEYRGTDVAQRAHGLRSAADILDA 60 Query: 61 EADEVARLIATEMGKTLTTAKYEALKSATGMRHFADHAQRYLSPETPVPASEVNASNLHV 120 E D +A + EMGKTL+ +K E K A G+R +ADH +L+ E A V AS Sbjct: 61 EVDTLAGTMTAEMGKTLSASKAEIAKCAKGLRFYADHGADFLADEA-ADAGAVGASRAFH 119 Query: 121 QFDPLGVVLAVMPWNYPLWQAVRFAAPALMAGNTGLLKHASNVPQCALYLGDLFARGGFP 180 ++ PLGVVLAVMPWN+PLWQ +RFAAP+LMAGN GLLKHASNVP+ ALYL DLF R G P Sbjct: 120 RYQPLGVVLAVMPWNFPLWQVIRFAAPSLMAGNVGLLKHASNVPRTALYLEDLFTRAGLP 179 Query: 181 EGAFQTLLVEGKDVIPLVDDARIRAVTLTGSVAAGSAIAEAAGRNIKRSVLELGGMDVFI 240 +GAFQTLLV + ++ D+R+ A TLTGS AG A+ AG +K+ VLELGG D F+ Sbjct: 180 KGAFQTLLVSSSQIEAILQDSRVAAATLTGSEGAGRAVGRTAGEALKKVVLELGGSDPFV 239 Query: 241 VMPSADIEKAAAQAVIARLQNSGQSCIAAKRFYVHEDVYDRFEHLFVTGMAEAVAGDPLD 300 V+PSAD+EKAA A AR QN+GQSCIAAKRF VH+DVYD F FV M E GDP D Sbjct: 240 VLPSADLEKAAQTATTARCQNNGQSCIAAKRFIVHQDVYDDFIAKFVARMGEQKVGDPTD 299 Query: 301 ESTSFGPLATERGRQDVHELVRDAREKGAAVQCGGEIPEGEGWYYPATVLTGVTEDMRIY 360 EST+ GPLATE+GRQDV +LV DA KGA V GG +P+G GW+YP TV+ G+TE+M +Y Sbjct: 300 ESTAVGPLATEQGRQDVIDLVDDAVAKGAEVLLGGTVPDGPGWFYPPTVIAGITEEMDLY 359 Query: 361 REECFGPVACLYKVSSLQEAIALSNDSDFGLSSSVWTNDETEATEAARSIEAGGVFINGL 420 EE FGPVA +YK + L EA+ L+N + FGL S+VWT D E EAG VF+NG+ Sbjct: 360 AEEVFGPVAAVYKAADLDEAVRLANVTRFGLGSNVWTTDPDEIERCIDDFEAGQVFVNGM 419 Query: 421 TASFPAVPFGGLKDSGYGRELSAYGIREFVNIKTVW 456 T S+P + FGG+KDSG+GREL+ +G+ EF N+KTVW Sbjct: 420 TTSYPELAFGGVKDSGHGRELTRHGMHEFCNLKTVW 455 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: 561 Number of extensions: 15 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