Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_053938969.1 WG78_RS16670 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_001294205.1:WP_053938969.1 Length = 466 Score = 330 bits (846), Expect = 6e-95 Identities = 172/449 (38%), Positives = 267/449 (59%), Gaps = 1/449 (0%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 +++G ++ + V NPAT +I+ IP + R+AI+AA+ A P W + A ER+ Sbjct: 14 FVNGAWIDADNQETVPVNNPATGEIIAHIPKLGKAETRRAIEAAQAAWPAWRSKTAKERS 73 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQS 129 LRK + + +++ ++ E GK A E+ + A YI++ AE ARR EG+II Sbjct: 74 QILRKWNDLMLANVDDLALILTSEQGKPLAEARGEITYAASYIEWFAEEARRIEGDIIAP 133 Query: 130 DRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFA 189 IL+ K+ +GVT I PWNFP +I RK+ PAL G +V+KP+ TP +A+A A Sbjct: 134 PSNDRRILVLKQPIGVTAAITPWNFPAAMITRKVGPALAAGCPMVLKPATQTPLSALALA 193 Query: 190 KIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVC 249 + + G+P G+FN++ G +G EL +P V ++ TGS G K++ +A I K+ Sbjct: 194 VLAERAGVPAGIFNVLTGSSTEIGGELTASPIVRKITFTGSTEVGAKLIEQSAPTIKKMS 253 Query: 250 LELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAM 309 +ELGG AP IV DDADL+ AV+ + S+ NSGQ C CA R+ VQ G+YD F +L +A+ Sbjct: 254 MELGGNAPFIVFDDADLDAAVQGAIGSKYRNSGQTCVCANRLLVQAGVYDAFAQKLADAV 313 Query: 310 QAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPTL 369 A++ GN + + + GPLI+ A+ ++E+ +A A +GA+V GGK G ++ PT+ Sbjct: 314 NALKVGNGVD-DGVTQGPLIDDKAIAKIEEHIADATGKGAQVLTGGKRHALGGTFFEPTI 372 Query: 370 LLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKG 429 L V M + EETFGP+ P+ F+T E+AI+MAND+++GL S YT++L + +G Sbjct: 373 LTGVTPAMKVAREETFGPLAPLFKFETEEEAIAMANDTEFGLASYFYTRDLARIFRVAEG 432 Query: 430 LKFGETYINRENFEAMQGFHAGWRKSGIG 458 L++G IN + G ++SG+G Sbjct: 433 LEYGMVGINAGLISSEVAPFGGVKQSGLG 461 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: 554 Number of extensions: 19 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: 479 Length of database: 466 Length adjustment: 33 Effective length of query: 446 Effective length of database: 433 Effective search space: 193118 Effective search space used: 193118 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