Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_193589538.1 MA_RS21285 aldehyde dehydrogenase family protein
Query= reanno::Smeli:SMc00781 (498 letters) >NCBI__GCF_000007345.1:WP_193589538.1 Length = 476 Score = 263 bits (671), Expect = 1e-74 Identities = 158/473 (33%), Positives = 254/473 (53%), Gaps = 7/473 (1%) Query: 8 IDGKRVAGTSGRVSNIFNPATGEVQGTVALASDADLAAAVESAKAAQPKWAATNPQRRAR 67 I+GK V G V I NPATGE+ V ++ D+A AVE+A +A WA+ +PQ+R Sbjct: 5 INGKAVEACGGEVFGIKNPATGELIEQVPRGTEEDVAVAVEAASSAFTGWASASPQQRGE 64 Query: 68 VFMKFVQLLNDNMNELAEMLSREHGKTIDDAKGDIVRGLEVCEFVIGIPHLQKSEFTEGA 127 V + +++ +ELA +L++E GK I +A+ +I V E+ G+ Q+ +F Sbjct: 65 VLYRAAEIVRQRKDELASLLTQEQGKPIVEARNEIEGFAHVLEYYCGLSGSQRGDFIPVP 124 Query: 128 GPGIDMYSIRQPVGIGAGITPFNFPGMIPMWMFAPAIACGNAFILKPSERDPSVPIRLAE 187 G G +++++P+G+ A I P+N P +I W AP + GN +LKP+ P + LA Sbjct: 125 GNGY-AFTVKKPLGVCAAIIPWNMPALIMGWKIAPVLISGNTLVLKPASNTPLTNLTLAS 183 Query: 188 LMIEAGLPAGILNVVNGDKGAV-DAILTHPDIAAVSFVGSTPIARYVYGTAAMNGKRAQC 246 + +EAGLPAG+LNVV G V ++++ P++ +SF G + V AA KR Sbjct: 184 IFVEAGLPAGVLNVVTGPGETVGESLVRSPEVRKISFTGEARTGKRVAELAACGMKRITL 243 Query: 247 FGGAKNHMIIMPDADLDQAANALIGAGYGSAGERCMAISVAVPVGEETANRLIDKLVPMV 306 G + M++ DADL+ AA + + + G+ C A+ + V E A I KL + Sbjct: 244 ELGGSDPMLVCDDADLESAAAGALRGRFYNCGQTCTAVK-RLYVFESVAEEFIKKLETGI 302 Query: 307 ESLRIGPYTDEKADMGPVVTKEAEQRIRSLIDSGIEQGA-KLVVDGRDFKLQGYENGHFI 365 +SLR+G D+ MGP+ + + I+ L E+ A +++ G+ + + E G+F Sbjct: 303 KSLRLGNGMDKNISMGPLNNRTQWEYIKELAAEIEEKDAGRIITGGKVPEFKDSEKGYFF 362 Query: 366 GGCLFDDVTPDMDIYKTEIFGPVLSVVRARNYEEALSLPMKHEYGNGVAIYTRDGDAARD 425 L DV D + K E+FGP+L VV +N +EA+ YG G +I+T++ D AR Sbjct: 363 EPTLVSDVPGDSRLLKEEVFGPLLPVVTVKNLDEAIVGANSTCYGLGASIWTKNIDRARK 422 Query: 426 FASRINIGMVGVNVPIPVPLAYHSFGGWKSSSFGDLNQHGTDSIKFWTRTKTI 478 ++N G++ +N + V FGG K S FG ++G +S+ + TKTI Sbjct: 423 GCEQLNAGIIWINQHLKVAPEV-PFGGVKESGFG--RENGPESLSEYLETKTI 472 Lambda K H 0.319 0.137 0.409 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: 569 Number of extensions: 33 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: 498 Length of database: 476 Length adjustment: 34 Effective length of query: 464 Effective length of database: 442 Effective search space: 205088 Effective search space used: 205088 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 (21.7 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