Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_073952689.1 RH94_RS37005 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_001906585.1:WP_073952689.1 Length = 494 Score = 296 bits (759), Expect = 8e-85 Identities = 162/472 (34%), Positives = 264/472 (55%), Gaps = 2/472 (0%) Query: 9 MYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIER 68 +YIDG++ R A + V +P T VI+ + D DA A+DAA RAQ W A P ER Sbjct: 22 LYIDGEWRPSRSGATVAVEDPGTRTVIAEVADADTADATDALDAAVRAQASWAATPPRER 81 Query: 69 ASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQ 128 LR+ I R ++++L+ E GK ++ EVA+ A+++ + +E A R +G + Sbjct: 82 GDVLRRAFEAIIARKDDLASLMTLEMGKPFAESQAEVAYAAEFLRWFSEEAVRIDGGYMT 141 Query: 129 SDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAF 188 + G ++ ++ +G + PWNFP + RK+ PAL G T+V+KP++ TP + +A Sbjct: 142 APGGGSRVVTMRQPVGPCLLVTPWNFPMAMGTRKIGPALAAGCTVVVKPAKQTPLSMLAL 201 Query: 189 AKIVDEIGLPRGVFNL-VLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITK 247 I+ E G P GV N+ R V L +P++ +S TGS G ++A +++N+ + Sbjct: 202 VDILREAGAPAGVVNVFTTNRSGEVTDHLLNDPRLRKLSFTGSTEVGRALLAKSSRNVLR 261 Query: 248 VCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGE 307 +ELGG AP +V DADL+ AV+ +++ N G+ C A R YVQ + D+F RL + Sbjct: 262 TSMELGGNAPFLVFADADLDAAVEGAFQAKMRNVGEACTAANRFYVQSPVADEFARRLAD 321 Query: 308 AMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPP 367 + A+ G+ + D +GPLI+A A++ V VA A GA V GG V G+++ P Sbjct: 322 RLAALPVGHGLD-PDTQVGPLIDANAVKNVTALVADATSAGATVLTGGGPVPSDGHFFAP 380 Query: 368 TLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAI 427 T+L V + EE FGPV P+VAFD + A+++ANDS+YGL ++T++L+ ++ Sbjct: 381 TVLEGVPLGARTLAEEIFGPVAPIVAFDDEDTAVALANDSEYGLAGYLFTESLSRGLRVS 440 Query: 428 KGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYLQS 479 + L+ G +N+ G ++SG+G G G+ EYL + + +++ Sbjct: 441 ERLECGMVGLNQGIISNPAAPFGGVKQSGLGREGGAVGIDEYLSVKYLAIKA 492 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: 546 Number of extensions: 24 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: 479 Length of database: 494 Length adjustment: 34 Effective length of query: 445 Effective length of database: 460 Effective search space: 204700 Effective search space used: 204700 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