Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_047213986.1 PATSB16_RS09910 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_001931675.1:WP_047213986.1 Length = 475 Score = 234 bits (598), Expect = 4e-66 Identities = 159/484 (32%), Positives = 252/484 (52%), Gaps = 24/484 (4%) Query: 9 YINGHKTNGVADSHQEVTNPATGQVTGQVALASQADVDSAVAAAQAAFPAWSDTPPIRRA 68 YING EV + AT + G++ +AD ++AVAAA+AAF AW+ TP + R Sbjct: 8 YINGQWVAPRGGDTIEVFHSATEEPMGRIPAGIEADAEAAVAAARAAFDAWAATPALERG 67 Query: 69 RVMFKFLELLNAHKDELAEAITREHGKVFTDAQGEVARGIDI--VEFACGIPQLLKGDYT 126 + K E L A DELA +IT E G +++R I + + G L G Y+ Sbjct: 68 AYLRKIAEGLRARTDELARSITGEVGMPI-----KLSRAIQVGGPVYNWGYYADLAGSYS 122 Query: 127 EQVSTGIDNWTTRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPSASLM 186 + G ++ R+P+GVV+ ITP+N+P+ A+AAG + VLKPS + P + + Sbjct: 123 YEERVG-NSLVVREPVGVVSAITPWNYPLNQITLKVAPALAAGCTVVLKPSEVAPFNAFI 181 Query: 187 MADLLKQAGLPDGVFNVVQGDKDSV-EALIDHPDVKALSFVGSTPIANLIYERGARSGKR 245 +A+++ +AGLP GVFN+V G V E L HPDV +SF GST + E A++ KR Sbjct: 182 LAEVIHEAGLPPGVFNLVTGYGPVVGEVLASHPDVDMVSFTGSTRAGKRVSELAAQTVKR 241 Query: 246 IQALGGAKNHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVPRLAE 305 + G K+ V++ DA+L AV + A Y ++G+ C A + ++ +++ + Sbjct: 242 VALELGGKSASVILDDADLPAAVKGTLNACYLNSGQTCSAHTRMLVPASRYEEVKALARQ 301 Query: 306 RARDLKIKNGLELDAEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSVTGEGCA 365 A + + E +GP+ ++ +R+ YI KG+ EGAE+V G + EG Sbjct: 302 LAESFVLGDPREETTRLGPLASAAQRERVLAYIRKGLEEGAELVTGGAE-----RPEGLD 356 Query: 366 DGFWMGGTLFDHVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFGNGVSCFTESG 425 GF++ T+ +V P T+ +EEIFGPVL + D A+++ ND +G G ++ Sbjct: 357 KGFFVRPTVLGNVAPRATVAQEEIFGPVLTIITYQDDDDAVRIANDSIYGLGGGVWSGDE 416 Query: 426 SVAREFGRRIQVGMVGIN---VPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTKQKS 482 + A RR++ G V IN + P FGG+K+S G+ G G+ + + KS Sbjct: 417 TRALAIARRMRTGQVDINGGQFNMQAP-----FGGFKQS--GNGRENGVYGLEEFLEYKS 469 Query: 483 IMQR 486 + R Sbjct: 470 LQFR 473 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: 559 Number of extensions: 27 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: 503 Length of database: 475 Length adjustment: 34 Effective length of query: 469 Effective length of database: 441 Effective search space: 206829 Effective search space used: 206829 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