Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_028311051.1 H566_RS0108130 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000482785.1:WP_028311051.1 Length = 484 Score = 320 bits (821), Expect = 5e-92 Identities = 178/466 (38%), Positives = 269/466 (57%), Gaps = 11/466 (2%) Query: 20 GDAWID--------VVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERASW 71 G AW+D +++PAT A + +P+ + R+AI AAE AQ +W ALPA R Sbjct: 17 GGAWLDADTGRATEILDPATGASLGTVPEMGEAETRRAIAAAEVAQKQWRALPAANRGRL 76 Query: 72 LRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQSDR 131 LR+ + E +++AL+ E GK A+ E+A+ A ++++ E A+R G++I S Sbjct: 77 LRRWYELMLEHQDDLAALMTAEQGKPLAEAKGEIAYAASFLEWFGEEAKRLYGDVIPSPA 136 Query: 132 PGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFAKI 191 +++ + +GVT I PWNFP +I RK AL G ++VIKP+ TP +A+A + Sbjct: 137 NDRRLVVVREPVGVTAAITPWNFPAAMITRKAGAALAAGCSMVIKPAPQTPFSALALVVL 196 Query: 192 VDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVCLE 251 + G+P GV N+V G +G EL NP V +S TGS G K+M A + K+ LE Sbjct: 197 AERAGIPAGVLNVVTGDAVAIGGELCRNPVVRKLSFTGSTGVGIKLMEQCAPTLKKLSLE 256 Query: 252 LGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAMQA 311 LGG AP IV DDAD++ AV + S+ N+GQ C CA R+ VQ GI+D FV +L EA++ Sbjct: 257 LGGNAPFIVFDDADVDAAVAGAMVSKYRNAGQTCVCANRLLVQDGIHDAFVAKLAEAVRT 316 Query: 312 VQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPTLLL 371 ++ G E + +GPLIN AA+ +VE+ +A A+ +GA V GGK G ++ PT++ Sbjct: 317 LKVGVGTEAG-VNLGPLINGAAVGKVERHLADALAKGASVVTGGKPHALGGNFFEPTIVT 375 Query: 372 DVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKGLK 431 V M++ EETFGP+ PV F T ++AI MAND+++GL + YT+++ + + L+ Sbjct: 376 GVTTAMAVAREETFGPLAPVFRFTTEDEAIRMANDTEFGLAAYFYTRDIGRVWRVGEALE 435 Query: 432 FGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYL 477 +G IN G + SG+G K+G EY T++ YL Sbjct: 436 YGMVGINTGLISNEVAPFGGIKASGLGREGSKYGCDEY--TEIKYL 479 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: 552 Number of extensions: 29 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: 484 Length adjustment: 34 Effective length of query: 445 Effective length of database: 450 Effective search space: 200250 Effective search space used: 200250 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