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_053938969.1 WG78_RS16670 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >NCBI__GCF_001294205.1:WP_053938969.1 Length = 466 Score = 234 bits (598), Expect = 4e-66 Identities = 144/453 (31%), Positives = 236/453 (52%), Gaps = 11/453 (2%) Query: 9 GGELIADTGRTADVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRAQVL 68 G + AD T V NP+TGE + +P + ++AI+AA+AA+PAWR+ +R+Q+L Sbjct: 17 GAWIDADNQETVPVNNPATGEIIAHIPKLGKAETRRAIEAAQAAWPAWRSKTAKERSQIL 76 Query: 69 FRFKQLLEANEERIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEYSRNVGP 128 ++ L+ AN + + +++ E GK + +A GE+ +E+ ++G+ Sbjct: 77 RKWNDLMLANVDDLALILTSEQGKPLAEARGEITYAASYIEWFAEEARRIEGDIIAPPSN 136 Query: 129 NIDAWSDFQPIGVVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIAELF 188 + QPIGV A ITP+NFPA + A+A G +LKP+ + P S L +A L Sbjct: 137 DRRILVLKQPIGVTAAITPWNFPAAMITRKVGPALAAGCPMVLKPATQTPLSALALAVLA 196 Query: 189 HEAGLPKGVLNVVHGDKGAVDA-LIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQALG 247 AG+P G+ NV+ G + L +P V+ ++F GST + + + K++ Sbjct: 197 ERAGVPAGIFNVLTGSSTEIGGELTASPIVRKITFTGSTEVGAKLIEQSAPTIKKMSMEL 256 Query: 248 GAKNHAVLMPDADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQIKG 307 G ++ DADLD AV +G+ Y + G+ C+ + + V + DA QKL + Sbjct: 257 GGNAPFIVFDDADLDAAVQGAIGSKYRNSGQTCVCAN-RLLVQAGVYDAFAQKLADAVNA 315 Query: 308 LKIGAGTSCGLDMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFLGGT 367 LK+G G G+ GPL+ A K+ +I +GA+++ G+ + + G F T Sbjct: 316 LKVGNGVDDGVTQGPLIDDKAIAKIEEHIADATGKGAQVLTGGKRHAL----GGTFFEPT 371 Query: 368 LFDRVTPEMTIYKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARLF-- 425 + VTP M + +EE FGP+ + + + EEA+ + ND E+G + +TRD AR+F Sbjct: 372 ILTGVTPAMKVAREETFGPLAPLFKFETEEEAIAMANDTEFGLASYFYTRD--LARIFRV 429 Query: 426 CDEIEVGMVGVNVPLPVPVAYHSFGGWKRSLFG 458 + +E GMVG+N L + FGG K+S G Sbjct: 430 AEGLEYGMVGINAGL-ISSEVAPFGGVKQSGLG 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: 581 Number of extensions: 33 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: 466 Length adjustment: 34 Effective length of query: 464 Effective length of database: 432 Effective search space: 200448 Effective search space used: 200448 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