Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_068105462.1 I601_RS01380 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_001653335.1:WP_068105462.1 Length = 506 Score = 223 bits (567), Expect = 2e-62 Identities = 146/484 (30%), Positives = 240/484 (49%), Gaps = 12/484 (2%) Query: 9 YINGHKTNGVADSHQEVTNPATGQVTGQVALASQADVDSAVAAAQAAFP--AWSDTPPIR 66 YI+G + + +++ PA G V+ + D +AV AA++AF W TP Sbjct: 5 YIDGTWRDAADGATRDIHCPADGHHVVTVSEGGEQDAVAAVVAARSAFDNGPWPHTPAPE 64 Query: 67 RARVMFKFLELLNAHKDELAEAITREHGKVFTDAQGEVARGIDIVEFACGIPQLLKGDYT 126 RA ++ + + L A KDE+A + + GK F ++Q +V + + + Q G Sbjct: 65 RAALLHRLADRLEADKDEVARLESLDTGKRFVESQIDVDDIVSVFRHFASLAQGEAGRVV 124 Query: 127 EQVSTGIDNWTTRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPSASLM 186 + G+ + +P+GV ITP+N+P++ W +AAGN+F+LKPS L PS ++ Sbjct: 125 DAGMPGVVSRVVHEPIGVCTLITPWNYPLLQTSWKVAPCLAAGNTFILKPSELTPSTAIW 184 Query: 187 MADLLKQAGLPDGVFNVVQGDKDSV-EALIDHPDVKALSFVGSTPIANLIYERGARSGKR 245 + L AGLPDGV N+V G D V L + P+V +SF G + A + K+ Sbjct: 185 LMGALSDAGLPDGVANLVLGAGDRVGPTLTEAPEVDLVSFTGGVVTGRRVMVAAAPTVKK 244 Query: 246 IQALGGAKNHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVPRLAE 305 + G KN V+ DA+LD A+D + A + +G+ C A + V+ V D++V L Sbjct: 245 VALELGGKNPNVIFADADLDAAIDNALTAVFLDSGQVCSAGARLVVEDTVHDQVVDELVR 304 Query: 306 RARDLKIKNGLELDAEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSVTGEGCA 365 RA +++ + DAE GP++++ ++ Y+ G+AEGA + V G + + G A Sbjct: 305 RAGRIRLGGPFDDDAETGPLISAAHRDKVEAYVAAGIAEGATLRVGGGRPEGAGYAAGLA 364 Query: 366 DGFWMGGTLFDHVTPEMTIYREEIFGPVLACVRVPD------VATAIQLINDHEFGNGVS 419 +GF+ T+ D + +M+ +EE FGPVL R A+ + ND +G + Sbjct: 365 EGFYYLPTILDDCSADMSCVQEESFGPVLTVERFTGEDADAREEAAVSIANDTVYGLAGA 424 Query: 420 CFTESGSVAREFGRRIQVGMVGINVPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTK 479 +T A R++ G + IN P +A +GG+K+S G G G+ Y + Sbjct: 425 VWTSDAGRAERVASRLRHGTIWINDYHPY-VAQAEWGGYKQS--GTGRELGIAGLEEYRE 481 Query: 480 QKSI 483 K I Sbjct: 482 TKHI 485 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: 630 Number of extensions: 28 Number of successful extensions: 2 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: 506 Length adjustment: 34 Effective length of query: 469 Effective length of database: 472 Effective search space: 221368 Effective search space used: 221368 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