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_034273494.1 AMYHA_RS20015 aldehyde dehydrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >NCBI__GCF_000504245.1:WP_034273494.1 Length = 454 Score = 215 bits (547), Expect = 3e-60 Identities = 150/462 (32%), Positives = 235/462 (50%), Gaps = 19/462 (4%) Query: 19 TADVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRAQVLFRFKQLLEAN 78 T DV NP+T + VR VPLA + +AI A A WR PA R ++L RF ++A+ Sbjct: 3 TFDVINPATEQLVRSVPLAGVDETSEAIARATRAQRRWRTVAPADRGRLLRRFADAVDAD 62 Query: 79 EERIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEYSRNVGPNIDAWSDF-Q 137 + +L G TI +A GE + + Y AAPE ++ R + F + Sbjct: 63 LGHLAELEVRNSGHTIGNARGEAGNVRDVLHYYAAAPE---RQFGRQIPVEGGVDITFAE 119 Query: 138 PIGVVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIAELFHEAGLPKGV 197 P+GVV I P+NFP + W + A+A GN +LKP+E P + L +AEL EAG+P+ V Sbjct: 120 PLGVVGIIVPWNFPMPIAAWGFAPALAAGNAAVLKPAELTPLTALRLAELAREAGIPEDV 179 Query: 198 LNVVHGDKGAV--DALIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQALGGAKNHAVL 255 V+ G KGAV + + P+V+ + F GST + + I + ++ KRV G K+ ++ Sbjct: 180 FQVIPG-KGAVVGERFVTHPDVRKVVFTGSTTVGKRIMAGCAEQVKRVTLELGGKSANIV 238 Query: 256 MPDADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQIKGLKIGAGTS 315 DADL+ A + + + G+ C A S + V + D + L P + G+K+G Sbjct: 239 FADADLERAAATAPYGVFDNAGQDCCARS-RILVQRDVVDDFMALLEPAVTGVKVGDPGD 297 Query: 316 CGLDMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFLGGTLFDRVTPE 375 +MGPL++ A R+ V ++ + V RG AG G++ T+ V E Sbjct: 298 ESTEMGPLISAAQRETVASFVPD------DAPVAFRGSCPAG--AGYWFPPTVLAPVDLE 349 Query: 376 MTIYKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARLFCDEIEVGMVG 435 ++EEIFGPV+ ++ + +A+++ ND +YG I+TRD A +E G + Sbjct: 350 SRAWREEIFGPVVAVMPFDDEADAIRIANDTDYGLAGSIWTRDVGKALRVARGVESGNLS 409 Query: 436 VNVPLPVPVAYHSFGGWKRSLFGDLHAYGPDGVRFYTKRKAI 477 VN V + FGG+K+S G GPD + +T+ K + Sbjct: 410 VNSHSAVRYS-TPFGGFKQSGLG--RELGPDALAAFTETKNV 448 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: 552 Number of extensions: 32 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: 454 Length adjustment: 33 Effective length of query: 465 Effective length of database: 421 Effective search space: 195765 Effective search space used: 195765 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: 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