Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_034271650.1 AMYHA_RS14120 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_000504245.1:WP_034271650.1 Length = 507 Score = 566 bits (1459), Expect = e-166 Identities = 281/504 (55%), Positives = 359/504 (71%), Gaps = 13/504 (2%) Query: 6 IEHYINGHKTNGVADSHQEVTNPATGQVTGQVALASQADVDSAVAAAQAAFPAWSDTPPI 65 I H+++G + G +D +VTNPATGQV+G+VALA + D +A+A A AW +T Sbjct: 5 IAHWVDGAEFAGTSDHWADVTNPATGQVSGRVALAGEHDAQHVIASAATAAKAWGETSLA 64 Query: 66 RRARVMFKFLELLNAHKDELAEAITREHGKVFTDAQGEVARGIDIVEFACGIPQLLKGDY 125 +R +++F F ELLN+ K+ELA IT EHGKV++DA GE+ RG ++VEFACGI LLKG Y Sbjct: 65 KRTQILFAFRELLNSRKEELAHLITAEHGKVYSDALGEITRGQEVVEFACGISHLLKGGY 124 Query: 126 TEQVSTGIDNWTTRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPSASL 185 +E STG+D + R PLGVV I+PFNFP MVPMW FP+AIA+GN+ VLKPS DPSA+L Sbjct: 125 SESASTGVDVHSKRDPLGVVGIISPFNFPAMVPMWFFPIAIASGNTVVLKPSEKDPSAAL 184 Query: 186 MMADLLKQAGLPDGVFNVVQGDKDSVEALIDHPDVKALSFVGSTPIANLIYERGARSGKR 245 +A+L K+AGLPDGVFNV+QGDK +V+AL+ DV A+SFVGSTPIA +YE +R GKR Sbjct: 185 WIANLWKEAGLPDGVFNVLQGDKVAVDALLHSQDVAAISFVGSTPIAKYVYEEASRHGKR 244 Query: 246 IQALGGAKNHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVPRLAE 305 +QALGGAKNHMVV+PDA+LD A DA + A YGSAGERCMAISV V V V D +V R+AE Sbjct: 245 VQALGGAKNHMVVLPDADLDLAADAAVNAGYGSAGERCMAISVLVAVDPVGDDLVARIAE 304 Query: 306 RARDLKIKNGLELD------AEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSV 359 R R L +G + D A+MGP+VT R+ G++ G GA++V+DGR +V Sbjct: 305 RTRTLVTGDGRKGDGPDGAEADMGPLVTKAHRDRVAGFVASGERAGAKLVIDGR----TV 360 Query: 360 TGEGCADGFWMGGTLFDHVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFGNGVS 419 G DG W+G TLFDHVTP+M IY EEIFGPVLA VR A++LIN +E+GNG + Sbjct: 361 EARGEQDGHWLGPTLFDHVTPDMDIYTEEIFGPVLAVVRASSYDEAVELINANEYGNGTA 420 Query: 420 CFTESGSVAREFGRRIQVGMVGINVPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTK 479 FT G AR F +QVGM+G+NVPIPVP+A++ FGGWKRS+FGDTHA+G EGV F+T+ Sbjct: 421 IFTNDGGAARRFESDVQVGMIGVNVPIPVPVAYYSFGGWKRSLFGDTHAHGTEGVHFFTR 480 Query: 480 QKSIMQRWSDSI---DAGAEFAMP 500 K + RW + + G E P Sbjct: 481 AKVVTTRWINPAARPEGGLELGFP 504 Lambda K H 0.319 0.136 0.406 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: 771 Number of extensions: 41 Number of successful extensions: 3 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: 503 Length of database: 507 Length adjustment: 34 Effective length of query: 469 Effective length of database: 473 Effective search space: 221837 Effective search space used: 221837 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