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_012469747.1 GLOV_RS08400 NADP-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >NCBI__GCF_000020385.1:WP_012469747.1 Length = 484 Score = 233 bits (594), Expect = 1e-65 Identities = 146/454 (32%), Positives = 238/454 (52%), Gaps = 7/454 (1%) Query: 6 HLIGGELIADTGRTADVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRA 65 +L G L AD+G+T DV NP+TGE + +P ++AI+AA AA+PAWR +RA Sbjct: 14 YLNGQWLAADSGKTIDVTNPATGEVLGTIPKMGTAETRRAIEAANAAWPAWRVKTAKERA 73 Query: 66 QVLFRFKQLLEANEERIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEYSRN 125 +L R+ +L+ N+E + +++ E GK + ++ GE+ +E+ + L G+ Sbjct: 74 TILRRWFELMLENQEDLAIIMTAEQGKPLAESRGEISYAASFIEWFAEEGKRLYGDTIPA 133 Query: 126 VGPNIDAWSDFQPIGVVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIA 185 G + +PIGV A ITP+NFP+ + A+A G T ++KP+ P S L +A Sbjct: 134 HGRDKRIVVIKEPIGVCAAITPWNFPSAMITRKAGPALAAGCTMVVKPATATPFSALALA 193 Query: 186 ELFHEAGLPKGVLNVVHGDKGAVDA-LIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQ 244 EL AG+P GV +V+ G + + P V+ L+F GST I + + ++ K+V Sbjct: 194 ELGERAGIPAGVFSVITGSSSEIGTEMTSNPIVRKLTFTGSTEIGKQLTAQCAATMKKVS 253 Query: 245 ALGGAKNHAVLMPDADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQ 304 G ++ DADLD AV + + Y + G+ C+ + + V + D +KL Sbjct: 254 MELGGNAPFIVFDDADLDAAVEGAIASKYRNTGQTCVCTN-RLLVQAGVYDLFAEKLATA 312 Query: 305 IKGLKIGAGTSCGLDMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFL 364 + +++G G + GPL+ A+ KV +I V++GA + + G+ +++ G F Sbjct: 313 VAKMRVGDGLKDDVQQGPLIDEASVQKVEEHIHDAVSKGARIALGGKRHEL----GGTFF 368 Query: 365 GGTLFDRVTPEMTIYKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARL 424 T+ VTP+M + +EE FGPV I + + EA+++ ND E+G + +TRD Sbjct: 369 QPTILCDVTPQMLVAREETFGPVAPIFKFTTDAEAIKMANDTEFGLASYFYTRDIGRVWR 428 Query: 425 FCDEIEVGMVGVNVPLPVPVAYHSFGGWKRSLFG 458 + +E GMVG+N L V FGG K S G Sbjct: 429 VAEALEYGMVGINTGL-VSTEIAPFGGVKESGIG 461 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: 579 Number of extensions: 22 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: 484 Length adjustment: 34 Effective length of query: 464 Effective length of database: 450 Effective search space: 208800 Effective search space used: 208800 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 Apr 09 2024. 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