Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_067907935.1 AQZ52_RS07360 aldehyde dehydrogenase family protein
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_001519075.1:WP_067907935.1 Length = 474 Score = 230 bits (586), Expect = 9e-65 Identities = 150/482 (31%), Positives = 241/482 (50%), Gaps = 23/482 (4%) Query: 9 NYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAVPRR 68 N I+GE V T + DV+NPA ++V+ QVP E++D A A AFKTWSK V R Sbjct: 7 NLIDGELVT--TAKALDVLNPANEQVIGQVPACGAEELDRAVAAARRAFKTWSKTPVDDR 64 Query: 69 ARILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMGDSLA 128 ++ + + +EL L+T E GK ++A E+G G ++M S Sbjct: 65 RAVIRAMAAAIDANFDELFRLLTAEQGKPHQQAQFEIG----------GCSAMMNAQSTL 114 Query: 129 SIATDVE-------AANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERT 181 ++ + + R P+GVVGGI P+NFP+++ AI G T +LKPS T Sbjct: 115 TLEETINEDSDERLSRTRRVPVGVVGGIVPWNFPVLMAVQKIAPAILSGCTIVLKPSPFT 174 Query: 182 PLLTEKLVELFEKAGLPKGVFNVVYGAHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGS 241 PL T + EL + +P GV N++ G + I HP+I I+F GS G+ + + S Sbjct: 175 PLTTLRFAELIKDI-VPAGVVNIITGEDALGPMITAHPDIDKITFTGSTATGKKIMEGAS 233 Query: 242 ENLKRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFM 301 ++LKR+ G + +IVL DA++ + ++F +AG+ C+A + + E I DE Sbjct: 234 KDLKRITLELGGNDASIVLPDADVAKVAEQLFWSSFTNAGQICVAAKRIYIHEDIYDELS 293 Query: 302 AKLQEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSDDG 361 A + E ++K+G+G + G +GP+ + R IE G + + G + S G Sbjct: 294 AAIAEYAKNVKVGDGSEQGTGVGPIQNKKQFDRVCELIEDAKTNGYKFLVGGDVDPSGSG 353 Query: 362 YFVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNSNA 421 Y+V TI DN + I +E F PV+ +++ + E I AN SE+ ++T ++ Sbjct: 354 YYVPITILDNPPEDARIVAEEQFGPVMPLMKFSSDDEVIARANNSEYGLAGAVWTKDTER 413 Query: 422 IRYFRENIDAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVVTARY 481 E ++ G + IN + F PF G K S FG + G + + +T +V+T + Sbjct: 414 GVKIAEQLETGTVWINEFLHL-SPFAPFGGHKQSGFGAEY--GIEGLKEFTYSQVITVKK 470 Query: 482 PA 483 A Sbjct: 471 DA 472 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: 546 Number of extensions: 23 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: 474 Length adjustment: 34 Effective length of query: 453 Effective length of database: 440 Effective search space: 199320 Effective search space used: 199320 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: 51 (24.3 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