Align Malonate-semialdehyde dehydrogenase; MSA dehydrogenase; EC 1.2.1.-; Methylmalonate-semialdehyde dehydrogenase; MMSA dehydrogenase; MSDH; EC 1.2.1.27 (uncharacterized)
to candidate WP_011938485.1 GURA_RS08035 aldehyde dehydrogenase family protein
Query= curated2:A7BJC4 (487 letters) >NCBI__GCF_000016745.1:WP_011938485.1 Length = 475 Score = 233 bits (595), Expect = 8e-66 Identities = 151/459 (32%), Positives = 242/459 (52%), Gaps = 12/459 (2%) Query: 5 RKLKNYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFETWSKVA 64 R+ + I GEW E V+NP ++ VP +T ED++ A +A + F+ S + Sbjct: 3 RRYRMLIGGEWSGDDRTGIE-VINPYDDSLIGIVPEATAEDVEAAIVSARKGFDEISAMP 61 Query: 65 VPRRARILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMG 124 +R+ IL + + + KEE+A +I E GK+ K AL E R E +FAA G Sbjct: 62 AYKRSEILERASEFIMRDKEEIAGIIAREAGKSWKYALAEAERSAETFKFAAIEARASHG 121 Query: 125 DSLASIATDVEAANY----RYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSER 180 + + A+ V A + R PIG++G I PFNFP+ + AIA GN +LKP+ + Sbjct: 122 EIVPMDASPVSAGRFGFYLRNPIGIIGAITPFNFPLNLVAHKLAPAIATGNAVVLKPATK 181 Query: 181 TPLLTEKLVELFEKAGLPKGVFNVVYGAHDVV-NGILEHPEIKAISFVGSKPVGEYVYKK 239 TPL + KL EL +AGLP G NV+ G+ V N ++E + I+F GS PVG + K Sbjct: 182 TPLTSLKLAELLMEAGLPAGALNVIIGSGATVGNRLVEDERLAMITFTGSPPVGRGI--K 239 Query: 240 GSEHLKRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADE 299 LKRV G+ + TI+ D +++ V+ V +F ++G+ C++ + V + +E Sbjct: 240 SRSGLKRVTLELGSNSPTIIEEDGDVDKAVSRCVIGSFANSGQVCISVQRIFVHQSRYEE 299 Query: 300 FMAKLQEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSD 359 F+AK E +K+G+ D +GP+I +R +S++E+ + GA + G NV Sbjct: 300 FIAKFVEATRSLKVGDPFDKTCDIGPMISRKELERAVSWLEEAKKLGAVIAVGG--NVV- 356 Query: 360 DGYFVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNS 419 G + PT+ +VT +M + E+FAP++SV+ K EA+E+A+ S + A ++TS+ Sbjct: 357 -GNCLEPTVLTSVTRDMQVMCSEVFAPIVSVLPYKTFDEALEMADDSIYGLQAGIYTSDI 415 Query: 420 NAIRYFRENIDAGMLGINLGVPAPMAFFPFSGWKSSFFG 458 N + +D G + IN + P+ G K S G Sbjct: 416 NKAFKAVKRLDVGGVIINDVPTFRVDHMPYGGNKESGLG 454 Lambda K H 0.318 0.136 0.397 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: 533 Number of extensions: 27 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: 487 Length of database: 475 Length adjustment: 34 Effective length of query: 453 Effective length of database: 441 Effective search space: 199773 Effective search space used: 199773 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 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