Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_167535078.1 SWIT_RS26765 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= reanno::Smeli:SMc00781 (498 letters) >NCBI__GCF_000016765.1:WP_167535078.1 Length = 500 Score = 635 bits (1639), Expect = 0.0 Identities = 315/496 (63%), Positives = 377/496 (76%), Gaps = 3/496 (0%) Query: 4 LGHFIDGKRVAGTSGRVSNIFNPATGEVQGTVALASDADLAAAVESAKAAQPKWAATNPQ 63 + +FI G A TS R+ ++F+PATG VQ V L+ +L AAV + +AAQP WAA NPQ Sbjct: 5 IDNFIGGHHQASTSTRLGDVFDPATGRVQAQVRLSDPTELDAAVANTQAAQPAWAAMNPQ 64 Query: 64 RRARVFMKFVQLLNDNMNELAEMLSREHGKTIDDAKGDIVRGLEVCEFVIGIPHLQKSEF 123 RRARV L+ +M+ELAEMLS EHGK D+KGDI RGL+V EF GIPHL K E+ Sbjct: 65 RRARVMFNLKALIEKHMDELAEMLSAEHGKVHSDSKGDIQRGLDVVEFACGIPHLLKGEY 124 Query: 124 TEGAGPGIDMYSIRQPVGIGAGITPFNFPGMIPMWMFAPAIACGNAFILKPSERDPSVPI 183 TEGAGPGID+YS+RQP+GI AGITPFNFP MIPMWMFAPAIACGNAFILKPSER+PSVP+ Sbjct: 125 TEGAGPGIDVYSMRQPIGIAAGITPFNFPAMIPMWMFAPAIACGNAFILKPSERNPSVPV 184 Query: 184 RLAELMIEAGLPAGILNVVNGDKGAVDAILTHPDIAAVSFVGSTPIARYVYGTAAMNGKR 243 RLAEL +EAGLPAGILNVV+GDK VDAIL +P I AVSFVGS+ IA+YVYG A NGKR Sbjct: 185 RLAELAMEAGLPAGILNVVHGDKQVVDAILDNPAIRAVSFVGSSDIAQYVYGRGASNGKR 244 Query: 244 AQCFGGAKNHMIIMPDADLDQAANALIGAGYGSAGERCMAISVAVPVGEETANRLIDKLV 303 QC GGAKNH I+MPDADLDQA ++GA YGSAGERCMA+ V VPVGE TA L KL Sbjct: 245 MQCMGGAKNHGIVMPDADLDQAVADILGAAYGSAGERCMALPVVVPVGEATAVALRAKLE 304 Query: 304 PMVESLRIGPYTDEKADMGPVVTKEAEQRIRSLIDSGIEQGAKLVVDGRDFKLQGYENGH 363 + LR+G +D A GPVV+ + RI + I +++G++LVVDGR F LQGYE+G Sbjct: 305 TGIAGLRVGVPSDPDAHYGPVVSSAHKARIENYIQLAVDEGSELVVDGRGFALQGYEDGF 364 Query: 364 FIGGCLFDDVTPDMDIYKTEIFGPVLSVVRARNYEEALSLPMKHEYGNGVAIYTRDGDAA 423 F+ L D V PDM Y EIFGPVL +VRA+ +EEALS P KH+YGNGVAI+TR+GD A Sbjct: 365 FLAPTLLDHVKPDMQSYNEEIFGPVLQMVRAQTFEEALSYPTKHQYGNGVAIFTRNGDYA 424 Query: 424 RDFASRINIGMVGVNVPIPVPLAYHSFGGWKSSSFGDLNQHGTDSIKFWTRTKTITSRWP 483 R F + + +GMVG+NVPIPVP++YHSFGGWK S FGD+NQ+G + ++F+TR KTIT RWP Sbjct: 425 RKFCANVEVGMVGINVPIPVPVSYHSFGGWKRSGFGDMNQYGMEGVRFYTRVKTITQRWP 484 Query: 484 SG--IKDGAEFSIPTM 497 SG + D F IPTM Sbjct: 485 SGGAVMD-QSFVIPTM 499 Lambda K H 0.319 0.137 0.409 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: 814 Number of extensions: 27 Number of successful extensions: 1 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: 498 Length of database: 500 Length adjustment: 34 Effective length of query: 464 Effective length of database: 466 Effective search space: 216224 Effective search space used: 216224 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 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