Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_084058850.1 B9A12_RS14640 L-glutamate gamma-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_900176285.1:WP_084058850.1 Length = 994 Score = 227 bits (578), Expect = 2e-63 Identities = 152/469 (32%), Positives = 238/469 (50%), Gaps = 15/469 (3%) Query: 4 PVQHPMYIDGQFVTWRGDAWIDVVNP-ATEAVISRIPDGQAEDARKAIDAAERAQPEWEA 62 PV+ P+ I+ + V + NP T+ V+ + + AR+A+ AA+ A W Sbjct: 503 PVKVPLVINDKKV--QTQETFSSTNPNRTDQVVGVVASAGEKKAREAVAAAKEAFAAWRD 560 Query: 63 LPAIERASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRY 122 P ERA +L + + R R E++AL V E GK + A+ +V D+++Y R Sbjct: 561 TPPRERAEYLFRAAQAARSRRYELAALQVYEVGKSWKEADGDVCEAIDFLEYYGREMIRL 620 Query: 123 EGEIIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTP 182 + PGE LF GV + PWNFPF + + AL+TGNT+V KP+ +P Sbjct: 621 GAPRRMGNVPGEVSHLFYEPRGVAAVVAPWNFPFAISVGMTSAALVTGNTVVYKPASQSP 680 Query: 183 NNAIAFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAA 242 +I E LP+GV N + G G +G L +P VAM++ TGS G +I+ AA Sbjct: 681 VIGYWLYRIFQEAKLPKGVLNFLPGPGAKIGDFLVTHPDVAMIAFTGSKEVGLRIIERAA 740 Query: 243 KN------ITKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKG 296 K + V E+GGK I+ DADL+ AV ++ S GQ C+ R+ V + Sbjct: 741 KTPPDAHFVKNVVAEMGGKNAIIIDADADLDEAVVHVLHSAFGYQGQKCSACSRLIVLEE 800 Query: 297 IYDQFVNRLGEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGK 356 Y + + RL A ++++ G P E MG +I+A A E++ + + EG + + Sbjct: 801 NYHKLLERLRAAAESLELG-PVEDAKNVMGAVIDAKAREKILEYIEIGKREGKVLV--ER 857 Query: 357 AVEG-KGYYYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSI 415 VEG GY+ P T+ D+R E + EE FGPVL V+ ++A+ +AN + Y LT ++ Sbjct: 858 PVEGSNGYFVPLTIFTDIRPEHRLAQEEIFGPVLSVMKVRDFDEALEVANSTQYALTGAV 917 Query: 416 YTQNLNVAMKAIKGLKFGETYINRENFEAMQGFH--AGWRKSGIGGADG 462 ++++ KA + + G YINR + A+ H G++ SG+G G Sbjct: 918 FSRSPENIEKARRRFRVGNLYINRGSTGAIVERHPFGGFKMSGVGSKAG 966 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: 1031 Number of extensions: 46 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: 994 Length adjustment: 39 Effective length of query: 440 Effective length of database: 955 Effective search space: 420200 Effective search space used: 420200 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: 54 (25.4 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