Align malonate-semialdehyde dehydrogenase (EC 1.2.1.15); malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18); methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_010532044.1 ON01_RS16145 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >NCBI__GCF_000224785.1:WP_010532044.1 Length = 480 Score = 231 bits (590), Expect = 3e-65 Identities = 143/454 (31%), Positives = 233/454 (51%), Gaps = 10/454 (2%) Query: 8 IGGELIADTGRTADVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRAQV 67 I G+ + T +V NP+ GE V VP + +QA++AA AF +W N RA Sbjct: 12 INGQWVGSDLDTLNVVNPANGETVGTVPNGGEKEAEQAVNAAYDAFESWSNLTAHDRAVY 71 Query: 68 LFRFKQLLEANEERIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEY--SRN 125 L + QL+ N+E + ++++ E GK I ++ GE+K +E+ + + G + Sbjct: 72 LKKLNQLMLENQEELAQMMTIEMGKPINESRGEVKYAASFIEWFAEEGKRIDGAVIPTHA 131 Query: 126 VGPNIDAWSDFQPIGVVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIA 185 G + W +P+GV A ITP+NFPA + A+A G TFI+KPS P + + + Sbjct: 132 AGKRLQVWK--KPVGVAAAITPWNFPAAMLTRKMGPALASGCTFIMKPSSESPLTAVKLM 189 Query: 186 ELFHEAGLPKGVLNVVHGDKGAV-DALIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQ 244 EL +AG PKGV+N+V G + ++E +V+ ++F GST + + + + + K++ Sbjct: 190 ELCEQAGFPKGVVNLVTGSSSKIAKVVMENSKVRKVTFTGSTEVGKTLIRQSADQVKKLS 249 Query: 245 ALGGAKNHAVLMPDADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQ 304 G V++ DAD+D AV + + + + G+ C+ + + V + + D V+KL Sbjct: 250 LELGGHAPLVVLDDADVDLAVKGTVASKFRNAGQTCICAN-RIYVQEGVYDEYVEKLTKA 308 Query: 305 IKGLKIGAGTSCGLDMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFL 364 ++ LK G GT D+GPL+ DKV ++D ++GA + G K G F Sbjct: 309 VEELKAGDGTDESNDIGPLINQDGLDKVKRHVDDATSKGASITTGG---KAVTDNGGLFY 365 Query: 365 GGTLFDRVTPEMTIYKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARL 424 T+ V M I +EE FGPV + +++S EEA++L ND YG +FT + Sbjct: 366 QPTVLKDVDQSMVIMEEETFGPVTPVEKISSDEEAVKLSNDTPYGLAAYVFTSNVARGYQ 425 Query: 425 FCDEIEVGMVGVNVPLPVPVAYHSFGGWKRSLFG 458 ++++ G+VG N P A FGG K S G Sbjct: 426 LIEKLDFGIVGWNEGGP-SAAQVPFGGMKESGIG 458 Lambda K H 0.319 0.137 0.411 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: 568 Number of extensions: 30 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: 498 Length of database: 480 Length adjustment: 34 Effective length of query: 464 Effective length of database: 446 Effective search space: 206944 Effective search space used: 206944 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 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