Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate N515DRAFT_0465 N515DRAFT_0465 aldehyde dehydrogenase (NAD+)
Query= BRENDA::P42412 (487 letters) >FitnessBrowser__Dyella79:N515DRAFT_0465 Length = 511 Score = 197 bits (500), Expect = 9e-55 Identities = 146/477 (30%), Positives = 218/477 (45%), Gaps = 10/477 (2%) Query: 13 GEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAVPRRARIL 72 GEW + VNPAT EV+ V S+ D + + A EAFKTW PRR + Sbjct: 23 GEWSRTSDAGALQPVNPATGEVIGTVHASSAADYETIVKRAQEAFKTWRTTPAPRRGEAV 82 Query: 73 FNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMGDSLASIAT 132 + L +HK+ L L+ +E GK E GEV I+ +FA G ++ G ++ S Sbjct: 83 RLCGEALRKHKDALGSLVALEMGKIKPEGDGEVQEMIDIADFAVGQSRMLYGYTMHSERP 142 Query: 133 DVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPL---LTEKLV 189 +P+G+VG I+ FNFP+ V W +A G+ I KPS +TPL T K+ Sbjct: 143 GHRMYEQYHPLGLVGIISAFNFPVAVWAWNAFLAAICGDICIWKPSPKTPLSAIATMKIC 202 Query: 190 -ELFEKAGLPKGVFNVVYGAHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGSENLKRVQ 248 E + G P F D+ G ++ I ISF GS VG V ++ + + R Sbjct: 203 NEALKAGGFPDIFFLFNDAGTDLSQGFVDDKRIPLISFTGSTKVGRMVGERVARRMGRSL 262 Query: 249 SLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFMAKL--QE 306 G N I+ A+L+ + IV A G+AG+RC + V E I E KL Sbjct: 263 LELGGNNAIILDASADLKLAIPAIVFGAVGTAGQRCTTTRRLFVHESIVGEVTDKLVAAY 322 Query: 307 KVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSDDGYFVGP 366 K + KIG+ +GP+ +D + L +EK G +++ G G FV P Sbjct: 323 KQVEGKIGDPTLATTLMGPLNSQDAVQAYLGAVEKAKASGGKVLTGGAALSDRKGNFVLP 382 Query: 367 TIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNSNAIRYFR 426 TI V + + E FAP+L ++ K+L EAIE+ N + +FT + A + Sbjct: 383 TIVTGVKNSDEVVQTETFAPILYIMPFKSLDEAIELQNDVPQGLSSAIFTRDLKAAEQYL 442 Query: 427 ENI--DAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVVTARY 481 + D G+ +N+G F G K + G +G D+ Y R++ T+ Y Sbjct: 443 SSAGSDCGIANVNIGTSGAEIGGAFGGEKET--GGGRESGSDAWKVYMRRQTNTSNY 497 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: 518 Number of extensions: 27 Number of successful extensions: 3 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: 511 Length adjustment: 34 Effective length of query: 453 Effective length of database: 477 Effective search space: 216081 Effective search space used: 216081 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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