Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_013420951.1 RVAN_RS17095 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= reanno::Smeli:SMc00781 (498 letters) >NCBI__GCF_000166055.1:WP_013420951.1 Length = 496 Score = 749 bits (1933), Expect = 0.0 Identities = 357/495 (72%), Positives = 419/495 (84%) Query: 3 ELGHFIDGKRVAGTSGRVSNIFNPATGEVQGTVALASDADLAAAVESAKAAQPKWAATNP 62 ELGHF+ GK +AG SGR +++FNPATG+V+ TVALA+ A++ AAVE+AKAAQP WAA NP Sbjct: 2 ELGHFVGGKMIAGQSGRFADVFNPATGKVEKTVALATKAEVRAAVENAKAAQPGWAAVNP 61 Query: 63 QRRARVFMKFVQLLNDNMNELAEMLSREHGKTIDDAKGDIVRGLEVCEFVIGIPHLQKSE 122 QRRARV M+FV+LL+ +M++LAE LSREHGKT DAKGDI+RGLEV EF IG PHL K E Sbjct: 62 QRRARVIMEFVRLLHRDMDKLAEALSREHGKTFPDAKGDIIRGLEVAEFCIGAPHLLKGE 121 Query: 123 FTEGAGPGIDMYSIRQPVGIGAGITPFNFPGMIPMWMFAPAIACGNAFILKPSERDPSVP 182 F+EG GPGID+YS+RQP+G+ AGITPFNFP MIPMW F PAIA GNAFILKPSER PSVP Sbjct: 122 FSEGVGPGIDIYSVRQPLGVVAGITPFNFPAMIPMWKFCPAIAAGNAFILKPSERAPSVP 181 Query: 183 IRLAELMIEAGLPAGILNVVNGDKGAVDAILTHPDIAAVSFVGSTPIARYVYGTAAMNGK 242 + LA LM EAGLP GILNVVNGDK AVDAIL DI AV FVGST IA Y+Y GK Sbjct: 182 LMLAALMQEAGLPDGILNVVNGDKEAVDAILDDTDICAVGFVGSTAIAEYIYTRGCAAGK 241 Query: 243 RAQCFGGAKNHMIIMPDADLDQAANALIGAGYGSAGERCMAISVAVPVGEETANRLIDKL 302 R QCFGGAKNHM+I PDADLDQ A+ALIGAGYG+AGERCMAISVAVP+G++TA+RL+++L Sbjct: 242 RVQCFGGAKNHMVIAPDADLDQVADALIGAGYGAAGERCMAISVAVPIGKDTADRLLERL 301 Query: 303 VPMVESLRIGPYTDEKADMGPVVTKEAEQRIRSLIDSGIEQGAKLVVDGRDFKLQGYENG 362 +P VE L++GPYT E D GP+VT +A++R+ L+D GI +GA LVVDGR F LQGYE+G Sbjct: 302 IPRVEKLKVGPYTSETVDFGPLVTADAKRRVLGLVDKGIAEGASLVVDGRGFSLQGYEDG 361 Query: 363 HFIGGCLFDDVTPDMDIYKTEIFGPVLSVVRARNYEEALSLPMKHEYGNGVAIYTRDGDA 422 F+G CLFD+V PDM+IYK EIFGPVLS+VRA YEEAL LPMKHEYGNGVAI+TRDGD Sbjct: 362 FFVGPCLFDNVKPDMEIYKAEIFGPVLSIVRADTYEEALDLPMKHEYGNGVAIFTRDGDT 421 Query: 423 ARDFASRINIGMVGVNVPIPVPLAYHSFGGWKSSSFGDLNQHGTDSIKFWTRTKTITSRW 482 ARDFASR+N+GMVG+NVPIPVPLA+++FGGWK S FGDLNQ G DS +F+T+TKTITSRW Sbjct: 422 ARDFASRVNVGMVGINVPIPVPLAHYTFGGWKRSGFGDLNQFGADSFRFYTKTKTITSRW 481 Query: 483 PSGIKDGAEFSIPTM 497 PSG+K+GA F IPTM Sbjct: 482 PSGVKEGASFVIPTM 496 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: 830 Number of extensions: 23 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: 496 Length adjustment: 34 Effective length of query: 464 Effective length of database: 462 Effective search space: 214368 Effective search space used: 214368 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