Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_034277076.1 AMYHA_RS13095 aldehyde dehydrogenase
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_000504245.1:WP_034277076.1 Length = 478 Score = 247 bits (630), Expect = 7e-70 Identities = 153/468 (32%), Positives = 244/468 (52%), Gaps = 8/468 (1%) Query: 15 WVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKT--WSKVAVPRRARIL 72 W + + D +PAT EVL VP +DID A + A +A + W++++ RAR+L Sbjct: 9 WCRAASGATFDSRDPATGEVLAVVPDGGSDDIDAAVRAARDALEDARWARISPAERARLL 68 Query: 73 FNFQQLLSQHKEELAHLITIENGKNTKEALG-EVGRGIENVEFAAGAPSLMMGDSLASIA 131 + +L+ +ELA L + + G+ A G VG E+ + AG + + G A Sbjct: 69 WRIAELIEDRADELAELESRDQGQPLALARGVSVGGAAEHFRYFAGWCTKLDGRVPAHSR 128 Query: 132 TDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPLLTEKLVEL 191 D R P+GV G I P+NFP+++ W A+A GNT +LKP+E+TPL +L L Sbjct: 129 PDALNYTKRVPVGVCGLITPWNFPLLIAAWKLAPALACGNTVVLKPAEQTPLTALRLAGL 188 Query: 192 FEKAGLPKGVFNVVYGAHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGSENLKRVQSLT 251 F +AG P GV NVV G + ++EH + +SF GS VG + + + NLKR+ Sbjct: 189 FHEAGFPPGVVNVVTGGPEAGRALVEHDGVDKVSFTGSTEVGRSIVRASAGNLKRLSLEL 248 Query: 252 GAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFMAKLQEKVADI 311 G K +++ D+++E V + +A ++G+ C A A V EF +L +I Sbjct: 249 GGKAASVITADSDIEAAVAGNLRSATQNSGQVCAASARFYVARARYSEFTDRLATAAENI 308 Query: 312 KIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGR--ENVSDDGYFVGPTIF 369 ++G GLD G +GP++ E++ SY+ G+E+GA LV G + G F PT+F Sbjct: 309 RLGPGLDPGTQMGPLVGEEHLSSVDSYVRSGIEQGASLVTGGARGDGPLARGSFYQPTVF 368 Query: 370 DNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNSNAIRYFRENI 429 + EM I ++EIF PVL+V+ ++ EA N S++ A ++T + E I Sbjct: 369 ADADDEMRIAREEIFGPVLTVMPFDDIDEAATRVNDSQYGLAASVWTRDLATAHRLAERI 428 Query: 430 DAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVV 477 +AG + +N+ A P+ G K+S +G G ++++ YT K V Sbjct: 429 NAGCVRVNMVAGIDPA-VPWGGVKASGWG--REMGAEAIEDYTEVKSV 473 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: 544 Number of extensions: 23 Number of successful extensions: 4 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: 478 Length adjustment: 34 Effective length of query: 453 Effective length of database: 444 Effective search space: 201132 Effective search space used: 201132 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