Align lactaldehyde dehydrogenase (EC 1.2.1.22); 2,5-dioxovalerate dehydrogenase (EC 1.2.1.26) (characterized)
to candidate WP_057507564.1 ABB28_RS04920 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= BRENDA::Q97UA1 (478 letters) >NCBI__GCF_001431535.1:WP_057507564.1 Length = 501 Score = 244 bits (624), Expect = 4e-69 Identities = 160/478 (33%), Positives = 251/478 (52%), Gaps = 17/478 (3%) Query: 10 KWIKGSGEEYLDI-NPADKDHVLAKIRLYTKDDVKEAINKAVAKFDEWSRTPAPKRGSIL 68 ++I+ S + D+ NPA +D VLA++ T +V +A+ A F W +TP R I Sbjct: 15 QFIESSTAHWQDVVNPATQD-VLAQVPFATTSEVDDAVAAAKEAFKTWRKTPIGTRARIF 73 Query: 69 LKAGELMEQEAQEFALLMTLEEGKTLKDSMFEVTRSYNLLKFYGALAFKISGKTLPSADP 128 LK +L+ + E A ++ E+GKT+ D+ +V R +++ A+ G+ + Sbjct: 74 LKYQQLIRENMSELAHTLSAEQGKTVPDAEGDVFRGLEVVEHAAAIGNLQLGELANNVAN 133 Query: 129 NTRIFTVKEPLGVVALITPWNFPLSIPVWKLAPALAAGNTAVIKPATKTPLMVAKLVEVL 188 +T+ +PLGV A ITP+NFP IP+W A+A GNT V+KP+ + P++ +LVE+ Sbjct: 134 GVDTYTLMQPLGVCAGITPFNFPAMIPLWMFPMAIATGNTFVLKPSEQDPMVTMRLVELA 193 Query: 189 SKAGLPEGVVNLVVGKGSEVGDTIVSDDNIAAVSFTGSTEVGKRIYKLVGNKNRMTRIQL 248 +AG+P+GV+N+V G G EV + I +I AVSF GST VG +Y + R+Q Sbjct: 194 LEAGIPKGVLNVVHG-GEEVVNAICDHPDIKAVSFVGSTRVGTHVYNRASLAGK--RVQC 250 Query: 249 ELGGKNALYVDKSADLTLAAELAVRGGFGLTGQSCTATSRLIINKDVYTQFKQRLLERVK 308 +G KN V A+ V FG GQ C A S L++ + + L+ + K Sbjct: 251 MMGAKNHAVVLPDANKEQTLNAMVGAAFGAAGQRCMAASTLVLVGEA-RSWVPDLVAKAK 309 Query: 309 KWRVGPGT-EDVDMGPVVDEGQFKKDLEYIEYGKNVGAKLIYGGN--IIPG--KGYFLEP 363 +V G+ D+GPV+ ++ I G GA L G + G KG F+ P Sbjct: 310 TLKVSAGSVAGTDVGPVISCSARERVEGLIASGLEQGATLDLDGRNPQVDGFEKGNFVGP 369 Query: 364 TIFEGVTSDMRLFKEEIFGPVLSVTEAKDLDEAIRLVNAVDYGHTAGIVASDIKAINEFV 423 TIF GVT+DMR+++EEIFGPVL + EA+ L++AI LVN+ G+ + A +F Sbjct: 370 TIFSGVTTDMRIYQEEIFGPVLVILEAETLEDAIALVNSNPNGNGTAVFTQSGAAARKFQ 429 Query: 424 SRVEAGVIKVNKPTVGLELQAPFGGFKNSGATTWKEM---GEDALEFYLKEKTVYEGW 478 ++ G + +N P + + P F S A+ ++ G+ + FY + KT+ W Sbjct: 430 EDIDVGQVGINVP---IPVPVPLFSFTGSRASKLGDLGPYGKQVVMFYTQTKTITARW 484 Lambda K H 0.316 0.135 0.389 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: 571 Number of extensions: 31 Number of successful extensions: 5 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: 478 Length of database: 501 Length adjustment: 34 Effective length of query: 444 Effective length of database: 467 Effective search space: 207348 Effective search space used: 207348 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 (21.6 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