Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_073948614.1 RH94_RS18135 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= reanno::pseudo5_N2C3_1:AO356_23175 (500 letters) >NCBI__GCF_001906585.1:WP_073948614.1 Length = 500 Score = 576 bits (1484), Expect = e-169 Identities = 274/481 (56%), Positives = 348/481 (72%) Query: 6 VVGHYIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPAWSEQSS 65 +V H+I G+ + V +PATG V +VA A VDAAVA+A A+ W + S Sbjct: 4 IVNHWIGGKTVEGASGTYGPVTDPATGEVTTKVAFASVEEVDAAVAAAKDAYATWGQSSL 63 Query: 66 LRRSRVMFKFKELLDRHHDELAQIISREHGKVLSDAHGEVTRGIEIVEYACGAPNLLKTD 125 +R+ ++FKF+ LLD H DE+A++I+ EHGKV SDA GEV RG+EIV+ ACG LK + Sbjct: 64 AQRTSILFKFRALLDAHRDEIAELITAEHGKVHSDALGEVARGLEIVDLACGINVQLKGE 123 Query: 126 FSDNIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERDPSAS 185 S + +D +RQPLGV AG+TPFNFP MVP+WM P+A+ GN F+LKPSE+DPSA+ Sbjct: 124 LSTQVATRVDVAGIRQPLGVVAGITPFNFPAMVPMWMFPIAIACGNTFVLKPSEKDPSAA 183 Query: 186 LLMARLLTEAGLPDGVFNVVQGDKVAVDALLQHPDIEAISFVGSTPIAEYIHQQGTAQGK 245 + +A LL EAGLPDGVFNV+ GDKVAVD LL+HPD++A+SFVGSTPIA YIH +A GK Sbjct: 184 VRIAELLAEAGLPDGVFNVLHGDKVAVDRLLEHPDVKAVSFVGSTPIARYIHTTASANGK 243 Query: 246 RVQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDELIAKLL 305 RVQALGGAKNHM+V+PDADLD AADA + AAYGSAGERCMAIS VAVG +GDEL+ K+ Sbjct: 244 RVQALGGAKNHMLVLPDADLDAAADAAVSAAYGSAGERCMAISAVVAVGSIGDELVEKIR 303 Query: 306 PRIDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFKVPGAEQGF 365 R +++KIG G P ++MGPL+T H+ KV +++ EGA +++DG G+ V G E G Sbjct: 304 ERAEKIKIGPGNDPASEMGPLITKAHRDKVASYVENAAGEGAEVVLDGTGYTVEGHEDGH 363 Query: 366 FVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCFTRDGGIA 425 ++G +L D+V YQ EIFGPVL ++RV + VALINA FGNG + FTRDGG A Sbjct: 364 WIGISLLDKVPTGAKAYQDEIFGPVLCVLRVDTYEEGVALINASPFGNGTAIFTRDGGAA 423 Query: 426 RAFARSIKVGMVGINVPIPVPMAWHSFGGWKRSLFGDHHAYGEEGLRFYSRYKSVMQRWP 485 R F I+ GMVG+NVPIPVP+ +HSFGGWK SLFGDHH YG +G FY+R K + RWP Sbjct: 424 RRFQLEIEAGMVGVNVPIPVPVGYHSFGGWKDSLFGDHHIYGNDGTHFYTRGKVITTRWP 483 Query: 486 D 486 D Sbjct: 484 D 484 Lambda K H 0.320 0.137 0.412 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: 741 Number of extensions: 25 Number of successful extensions: 1 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: 500 Length of database: 500 Length adjustment: 34 Effective length of query: 466 Effective length of database: 466 Effective search space: 217156 Effective search space used: 217156 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 (21.8 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