Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_035133104.1 Q763_RS08225 aldehyde dehydrogenase family protein
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_000769915.1:WP_035133104.1 Length = 515 Score = 209 bits (532), Expect = 2e-58 Identities = 145/482 (30%), Positives = 236/482 (48%), Gaps = 21/482 (4%) Query: 9 NYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAVPRR 68 ++ NGE +ES +P ++ +V ST+ED + A A EAFK+W V P+R Sbjct: 32 SFANGEIIES--------YSPVDGTLIAKVKASTQEDYEAAVAKAQEAFKSWRLVPAPKR 83 Query: 69 ARILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMGDSLA 128 I+ + L ++KE L L++ E GK+ +E LGEV I+ +FA G + G ++ Sbjct: 84 GEIVRQMGEELRKYKEPLGQLVSYEMGKSLQEGLGEVQEMIDICDFAVGLSRQLYGLTMH 143 Query: 129 SIATDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPLL---T 185 S +P+G+VG I+ FNFP+ V W +A G+ I KPSE+TPL Sbjct: 144 SERPMHRMYEQYHPVGIVGIISAFNFPVAVWSWNAMLAWVCGDVCIWKPSEKTPLCGIAC 203 Query: 186 EKLVE-LFEKAGLPKGVFNVVYGAHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGSENL 244 + +++ + E+ +P+GV ++ G D + + + +SF GS VG +V K +E Sbjct: 204 QNIIKTVLERNNIPEGVSCLING-RDNGDRMNTDKRLPLVSFTGSTRVGRHVSKTVAERF 262 Query: 245 KRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFMAKL 304 G N IV A++ + V A G+AG+RC + V E + D+ + L Sbjct: 263 GNTILELGGNNAIIVSEHADINMVLVGAVFGAVGTAGQRCTTTRRLIVHESVYDKTIEVL 322 Query: 305 QEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDG---RENVSDDG 361 + +KIGN LD +GP+I +D+ + L IEK +EG ++ +G + + G Sbjct: 323 KSAYGQLKIGNPLDSNNHVGPLIDKDSVQNYLDAIEKAKQEGGNVIVEGGVMQGEGYESG 382 Query: 362 YFVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNSNA 421 +V P I + I + E FAP+L V++ +L+EAI + N + +FTSN Sbjct: 383 CYVKPCIIE-AKNSFEIVQHETFAPILYVMKYNDLEEAIAMQNDVPQGLSSSIFTSNMRE 441 Query: 422 IRYFRENI--DAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVVTA 479 + F + D G+ +N+G F G K + G +G D+ Y R++ T Sbjct: 442 MELFLSHAGSDCGIANVNIGTSGAEIGGAFGGEKET--GGGRESGSDAWKAYMRRQTNTI 499 Query: 480 RY 481 Y Sbjct: 500 NY 501 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: 557 Number of extensions: 34 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: 515 Length adjustment: 34 Effective length of query: 453 Effective length of database: 481 Effective search space: 217893 Effective search space used: 217893 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