Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_013721829.1 ALIDE2_RS08540 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000204645.1:WP_013721829.1 Length = 489 Score = 300 bits (768), Expect = 7e-86 Identities = 168/458 (36%), Positives = 251/458 (54%), Gaps = 5/458 (1%) Query: 22 AWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERASWLRKISAGIRE 81 A + V +PAT A I+ +PD A +AR A+DAA A P W +PA +RA+ ++ + Sbjct: 27 ARLAVTDPATGAAITDVPDSGAAEARAALDAAHAAFPAWRKVPAKQRAAIIKLWHDLVMA 86 Query: 82 RASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQSDRPGENILLFKR 141 ++ LI E GK + EVA+ A YI++ E A R GE+I + PG + + Sbjct: 87 HQDDLGKLISREQGKPLAEGKGEVAYAASYIEWFGEEATRMNGEVIPAPVPGRRMFALRE 146 Query: 142 ALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFAKIVDEIGLPRGV 201 +GV I PWNFP +IARK+APAL G T+V KP+E TP ++A + E G+P GV Sbjct: 147 PVGVVAAITPWNFPAAMIARKIAPALAAGCTVVCKPAEDTPLTSLALVLLAHEAGVPPGV 206 Query: 202 FNLVLGRGETVGQEL---AGNPKVAMVSMTGSVSAGEKIMATAAKNITKVCLELGGKAPA 258 N+V E + + + +V ++ TGS G+ + +A + K+ LELGG AP Sbjct: 207 LNIVTASREKTPEVVDVWLDDARVRKITFTGSTPVGKHLARRSADTLKKLSLELGGNAPF 266 Query: 259 IVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAMQAVQFGNPA 318 IV DDAD++ AV+ + ++ N GQ C C RV+V + ++D F +L + A++ G PA Sbjct: 267 IVFDDADVDAAVEGFMAAKFRNGGQTCVCPNRVFVHRAVFDSFAQKLAARVGALKVG-PA 325 Query: 319 ERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKG-YYYPPTLLLDVRQEM 377 +GP+IN A+E++E+ V A+ +GARV GGK + G YY PT+L M Sbjct: 326 SDPASQIGPMINGRAVEKIERHVQDAIAKGARVLTGGKRLPELGPTYYAPTVLTGADPTM 385 Query: 378 SIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKGLKFGETYI 437 + EETFGPV P+ FD + + AND+ +GL + Y+Q++ + L+ G I Sbjct: 386 ACACEETFGPVAPLTVFDDEAEVVQAANDTPFGLAAYFYSQDVRRIWRVADALESGIVGI 445 Query: 438 NRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVV 475 N A G ++SG G HGL +YL T+ V Sbjct: 446 NEGAISAEAAPFGGVKESGYGREGSTHGLDDYLHTKYV 483 Lambda K H 0.318 0.135 0.392 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: 569 Number of extensions: 26 Number of successful extensions: 4 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: 479 Length of database: 489 Length adjustment: 34 Effective length of query: 445 Effective length of database: 455 Effective search space: 202475 Effective search space used: 202475 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 Apr 09 2024. 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