Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_010529728.1 ON01_RS04100 betaine-aldehyde dehydrogenase
Query= BRENDA::Q9EQ20 (535 letters) >NCBI__GCF_000224785.1:WP_010529728.1 Length = 489 Score = 238 bits (608), Expect = 3e-67 Identities = 148/484 (30%), Positives = 253/484 (52%), Gaps = 9/484 (1%) Query: 41 KLFIDGKFVESKSDKWIDIHNPATNEVVGRVPQSTKAEMDAAVESCKRAFPA--WADTSI 98 K IDG +V S SD DI NP ++V V +S +++ AA+ + ++AF WA T Sbjct: 5 KQLIDGSWVTSNSDAVRDIINPFNQKIVATVTESDESDTKAAITAARKAFDQGDWATTPA 64 Query: 99 LSRQQVLLRYQQLIKENLKEIARLITLEQGKTLADAEGDVFRGLQVVEHACSVTSLMLGE 158 R +++ + LI+ + +E+A L +L+ GKT+ ++ GD+ V + + GE Sbjct: 65 AERGKIVHKIADLIERDREELAELESLDTGKTVEESLGDMDDIAGVFRYFAEMADKDGGE 124 Query: 159 TMPSITKDMDLYSYRLPLGVCAGIAPFNFPAMIPLWMFPMAMVCGNTFLMKPSERVPGAT 218 + S + P+GVC I P+N+P + W A+ GNT +MKPSE P + Sbjct: 125 IIESPIPNSTSKVVHEPVGVCGQITPWNYPLLQASWKLAPALAAGNTLVMKPSEITPLTS 184 Query: 219 MLLAKLLQDSGAPDGTLNIIHGQHDAVNF-ICDHPDIKAISFVGSNQAGEYIFERGSRNG 277 + + +L+ ++G P G +N++ G D+V + + ++ ISF G G+ I + S N Sbjct: 185 IKVFELMAEAGVPAGVVNLVLGPGDSVGAELSANDNVDLISFTGGIHTGKKIMQAASSNV 244 Query: 278 KRVQANMGAKNHGVVMPDANKENTLNQLVGAAFGAAGQRCMALSTAILVGEA--KKWLPE 335 K + +G KN +V DA+ E ++Q + A F AGQ C A T +++ E+ ++ Sbjct: 245 KNLALELGGKNPNIVFADADFETAVDQAMNAVFFHAGQICSA-GTRLIIEESIHDAFVSA 303 Query: 336 LVDRAKNLRVNAGDQPGADLGPLITPQAKERVCNLIDSGTKEGASILLDGRRIKVKGYEN 395 +VDR KN+++ +G +GPLI+ +V N +++G +EGA++ + G R +N Sbjct: 304 IVDRVKNIKLGSGFDESTQMGPLISEDHLNKVVNYVENGKQEGATVAVGGSRPDDPELQN 363 Query: 396 GNFVGPTIISNVKPSMTCYKEEIFGPVLVVLETETLDEAIKIVNDNPYGNGTAIFTTNGA 455 G F PTI++ M ++E FGPV+ V + T +EA+++ ND+ YG +FT + A Sbjct: 364 GLFYLPTILTGCTSDMRVVQDEGFGPVITVEKFTTEEEAVRLANDSIYGLSGGVFTNDIA 423 Query: 456 TARKYAHMVDVGQVGVNVPIPVPLPMFSFTGSRSSFRGDTNFYGKQGIQFYTQLKTITSQ 515 A + + +G V +N + + P + G + S G GK G++ Y + K I Sbjct: 424 KAERCVAKLRMGTVWIN-DVNLYFPHAPWGGYKQS--GIGRELGKTGLEEYQETKHIFQN 480 Query: 516 WKEE 519 K E Sbjct: 481 LKPE 484 Lambda K H 0.318 0.133 0.391 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: 19 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: 535 Length of database: 489 Length adjustment: 35 Effective length of query: 500 Effective length of database: 454 Effective search space: 227000 Effective search space used: 227000 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 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