Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_068863622.1 I603_RS07320 aldehyde dehydrogenase family protein
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_001677335.1:WP_068863622.1 Length = 506 Score = 223 bits (568), Expect = 1e-62 Identities = 157/488 (32%), Positives = 243/488 (49%), Gaps = 19/488 (3%) Query: 6 KLKNYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAV 65 K N+I G+WV QY D ++P + +CQV + EDI+ A A +A W + + Sbjct: 18 KYDNFIGGQWVAPVKCQYFDNISPVNGKRVCQVARGSAEDIELALDAAHKARAAWGRTST 77 Query: 66 PRRARILFNFQQLLSQHKEELAHLITIENGKNTKE-ALGEVGRGIENVEFAAGAPSLMMG 124 R+ IL Q + + + LA + TI+NGK +E ++ +++ + AGA G Sbjct: 78 TERSNILNRIAQRIEDNLDLLALVETIDNGKPIRETTAADLPLAVDHFRYFAGALRAQEG 137 Query: 125 DSLASIATDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPLL 184 ++ I D A ++ P+GVVG I P+NFP+++ W A+A GN +LKP+E+TP+ Sbjct: 138 -GISEIDHDTIAYHFHEPLGVVGQIIPWNFPLLMAVWKLAPALAAGNCVVLKPAEQTPMS 196 Query: 185 TEKLVELFEKAGLPKGVFNVVYG-AHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGSEN 243 L+E+ LP+GV NVV G + + P I I+F G G + + SEN Sbjct: 197 IMVLMEVIGDL-LPEGVVNVVNGFGIEAGKPLATSPRIAKIAFTGETTTGRLIMQYASEN 255 Query: 244 LKRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSA------GERCMACAVVTVEEGIA 297 L G K+ I D ED + A G A GE C + + E I Sbjct: 256 LIPCTLELGGKSPNIFFADVMREDD-DYLDKALEGFAMFALNQGEVCTCPSRALIHESIY 314 Query: 298 DEFMAKLQEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENV 357 D FM K +V IK+G+ LD +G D ++ LSYIE G EGA+++ G ++ Sbjct: 315 DRFMEKAIARVNAIKLGSPLDAATMIGAQASNDQLEKILSYIEIGKGEGAKVLTGGGRHI 374 Query: 358 SD----DGYFVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGAC 413 + +GY+V PT+ + +M I+++EIF PVLSV K+ EA+ IAN + + GA Sbjct: 375 HEGELAEGYYVKPTVLEG-HNKMRIFQEEIFGPVLSVTTFKDNDEALSIANDTLYGLGAG 433 Query: 414 LFTSNSNAIRYFRENIDAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTR 473 +++ ++N F I+AG + N P A F G+K S G N K ++ Y + Sbjct: 434 VWSRDANTCYRFGRAIEAGRVWTNCYHAYP-AHAAFGGYKQSGIG--RENHKMMLEHYQQ 490 Query: 474 KKVVTARY 481 K + Y Sbjct: 491 TKNLLVSY 498 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: 573 Number of extensions: 26 Number of successful extensions: 5 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: 506 Length adjustment: 34 Effective length of query: 453 Effective length of database: 472 Effective search space: 213816 Effective search space used: 213816 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