Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_010531948.1 ON01_RS15275 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_000224785.1:WP_010531948.1 Length = 488 Score = 707 bits (1824), Expect = 0.0 Identities = 337/478 (70%), Positives = 411/478 (85%), Gaps = 2/478 (0%) Query: 6 KLKNYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAV 65 +LKNYI G+W+E+K+D+ E V+NPAT EV+ +VPIS+ ED+D+A + A EAF+ W ++AV Sbjct: 10 QLKNYIGGKWIEAKSDKTESVINPATGEVIAEVPISSNEDVDHAVEVAHEAFQDWKELAV 69 Query: 66 PRRARILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMGD 125 P+RARILF +QQLL H +ELA LITIENGKN KEA GEV RGIENVEFAAGAP+LMMGD Sbjct: 70 PKRARILFKYQQLLVDHWDELAELITIENGKNLKEAKGEVQRGIENVEFAAGAPNLMMGD 129 Query: 126 SLASIATDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPLLT 185 L+SIA+ +E+ YRYPIGVVGGI PFNFPMMVPCWMFPMAIA GNTFI+KPSERTPLL Sbjct: 130 QLSSIASGLESGVYRYPIGVVGGITPFNFPMMVPCWMFPMAIATGNTFIMKPSERTPLLA 189 Query: 186 EKLVELFEKAGLPKGVFNVVYGAHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGSENLK 245 +L EL E+AGLP+GVFN+V+GAHDVVNG+L+H ++ AISFVGS+PV E+VYK+G++NLK Sbjct: 190 NRLAELLEEAGLPEGVFNIVHGAHDVVNGLLDHDKVAAISFVGSQPVAEHVYKRGTDNLK 249 Query: 246 RVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFMAKLQ 305 RVQ+L+GAKNHTIVLNDAN+++ T I+ AAFGSAGERCMA +VV VEE +ADEF+ +L Sbjct: 250 RVQALSGAKNHTIVLNDANMDNASTQILNAAFGSAGERCMAASVVAVEESVADEFIDQLI 309 Query: 306 EKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRE--NVSDDGYF 363 +K +I IGNGLD+ VFLGPVIRE +K+RTL YIE G EGA+L+ DGRE N + GYF Sbjct: 310 KKANEINIGNGLDEDVFLGPVIREQHKERTLGYIETGENEGAKLIRDGREDGNAQEKGYF 369 Query: 364 VGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNSNAIR 423 VGPTIFDNVTTEM IW++EIFAPVLS++RVK+L EAI++ N+S FANG+CLFT + ++R Sbjct: 370 VGPTIFDNVTTEMKIWQEEIFAPVLSIVRVKDLDEAIDVTNQSPFANGSCLFTRDGGSVR 429 Query: 424 YFRENIDAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVVTARY 481 FRENIDAGMLGIN+GVPAPMAFFPFSGWK SF+G LHANGKDSV+FYTRKKV+T R+ Sbjct: 430 QFRENIDAGMLGINIGVPAPMAFFPFSGWKDSFYGDLHANGKDSVEFYTRKKVMTTRW 487 Lambda K H 0.318 0.136 0.396 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: 741 Number of extensions: 33 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: 487 Length of database: 488 Length adjustment: 34 Effective length of query: 453 Effective length of database: 454 Effective search space: 205662 Effective search space used: 205662 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: 52 (24.6 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