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_012755384.1 RLEG_RS24785 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >NCBI__GCF_000023185.1:WP_012755384.1 Length = 495 Score = 228 bits (581), Expect = 4e-64 Identities = 147/440 (33%), Positives = 221/440 (50%), Gaps = 8/440 (1%) Query: 21 DVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRAQVLFRFKQLLEANEE 80 +V +PST + VP A A++AA +A +WR TPP KR+++L R +L+ E Sbjct: 40 EVIDPSTEAVIAAVPDATLADAAAAVEAAASAAESWRETPPRKRSEILRRCFELMVERSE 99 Query: 81 RIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEYSRNVGPNIDAWSDFQPIG 140 + +LIS E+GK + DA GE+ E + + GE+ D+QPIG Sbjct: 100 TLARLISLENGKALRDARGEVAYAAEFFRWNAEEAVRISGEFGLAPAGGNRIVVDYQPIG 159 Query: 141 VVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIAELFHEAGLPKGVLNV 200 + ITP+NFPA + A+A G T ILKP+ P + +A L+ EAG+P GV+NV Sbjct: 160 ICVLITPWNFPAAMATRKIAPALAAGCTVILKPASETPLTAYALAALYEEAGVPPGVVNV 219 Query: 201 VHGDK--GAVDALIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQALGGAKNHAVLMPD 258 + + A++ P V+ LSF GST + + +E K G V+ D Sbjct: 220 MTTSTPGPVIAAMLADPRVRKLSFTGSTGVGRMLLAEAAKNVISCSMELGGNAPFVVFDD 279 Query: 259 ADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQIKGLKIGAGTSCGL 318 AD+D A+ LM A + GE C A + + + I DA +K ++ L +G+G Sbjct: 280 ADIDAAIEGLMVAKMRNAGEACTAAN-RIYIQSGIHDAFAKKFTQRMAALNVGSGVDADT 338 Query: 319 DMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFLGGTLFDRVTPEMTI 378 + GP++T A +K+ ++ +++GA ++ GR +AG GFF T+ V+P + Sbjct: 339 ECGPMITRKAVEKIERLVEDAISRGARVLCGGR--SLAG--RGFFYRPTVLVDVSPASDM 394 Query: 379 YKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARLFCDEIEVGMVGVNV 438 EEIFGPV + R S E + ND EYG I+TRD +IE GM+ +N Sbjct: 395 GCEEIFGPVAPLYRFESEAEVIAAANDTEYGLAAYIYTRDIGRGMRVASKIEAGMIALNR 454 Query: 439 PLPVPVAYHSFGGWKRSLFG 458 L V FGG K+S G Sbjct: 455 GL-VSDPAAPFGGVKQSGLG 473 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: 604 Number of extensions: 32 Number of successful extensions: 6 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: 495 Length adjustment: 34 Effective length of query: 464 Effective length of database: 461 Effective search space: 213904 Effective search space used: 213904 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