Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_068173812.1 HTA01S_RS16360 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_001592305.1:WP_068173812.1 Length = 483 Score = 270 bits (689), Expect = 1e-76 Identities = 181/481 (37%), Positives = 242/481 (50%), Gaps = 20/481 (4%) Query: 8 HYINGH----KTNGVADSHQEVTNPA-TGQVTGQVALASQADVDSAVAAAQAAFPAWSDT 62 H+ING T GV+ TNP+ T +V + A A + + A+ AA A P WS + Sbjct: 12 HFINGRWEIGTTTGVS------TNPSDTREVVAEYARADRNQTELAIRAAADALPHWSQS 65 Query: 63 PPIRRARVMFKFLELLNAHKDELAEAITREHGKVFTDAQGEVARGIDIVEFACGIPQLLK 122 P RRA V+ + L A KDEL + RE GK + GEVAR I +F G + Sbjct: 66 SPQRRADVLDQIGSELLARKDELGALLAREEGKTLPEGVGEVARAGQIFKFFAGEALRIP 125 Query: 123 GDYTEQVSTGIDNWTTRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPS 182 G+ V G+ TR+P+GVV I P+NFP +P W A+A GN+ V KP+ L P+ Sbjct: 126 GEVIASVRPGVRVDVTREPVGVVGIIAPWNFPFAIPAWKIAPALAYGNTVVFKPAELVPA 185 Query: 183 ASLMMADLLKQAGLPDGVFNVVQGDKDSV-EALIDHPDVKALSFVGSTPIANLIYERGAR 241 +A+++ + GLP GVFN+V G V + L+DHP V ALSF GS I + Sbjct: 186 CGWALAEIISRCGLPAGVFNLVMGSGREVGQTLVDHPLVNALSFTGSVSTGERILKAATA 245 Query: 242 SGKRIQALGGAKNHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVP 301 ++Q G KN +VV+ DA+LD+AVD + +Y S G+RC A S ++ V D V Sbjct: 246 RRAKVQLEMGGKNPLVVLADADLDQAVDCALQGSYFSTGQRCTASSRLIVQAQVHDAFVA 305 Query: 302 RLAERARDLKIKNGLELDAEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSVTG 361 +L +R LK+ + LE EMGP+V ++ YIE EGAE V G D T Sbjct: 306 KLRQRLSTLKVGHALERGTEMGPVVDRAQLEQNLAYIEIARNEGAEHVWGG-DLLQRPT- 363 Query: 362 EGCADGFWMGGTLFDHVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFGNGVSCF 421 G +M LF PE + REEIFGPV +R D A+ L ND FG Sbjct: 364 ----PGHYMSPALF-LAKPEHRVAREEIFGPVACVLRADDYEHALVLANDTPFGLCAGIC 418 Query: 422 TESGSVAREFGRRIQVGMVGINVPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTKQK 481 T S A F R +VGM +N+P FGG K S G + G V FYT K Sbjct: 419 TTSLKYAMHFKRHAEVGMTMVNLPTAGVDFHVPFGGRKESSHG-SREQGRYAVEFYTTVK 477 Query: 482 S 482 + Sbjct: 478 T 478 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: 608 Number of extensions: 29 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: 483 Length adjustment: 34 Effective length of query: 469 Effective length of database: 449 Effective search space: 210581 Effective search space used: 210581 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 Apr 09 2024. 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