Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_053544403.1 CDES_RS04150 NAD-dependent succinate-semialdehyde dehydrogenase
Query= reanno::pseudo6_N2E2:Pf6N2E2_515 (500 letters) >NCBI__GCF_001277995.1:WP_053544403.1 Length = 483 Score = 209 bits (533), Expect = 1e-58 Identities = 142/458 (31%), Positives = 224/458 (48%), Gaps = 13/458 (2%) Query: 8 GHYLNGHVQDHDSTRFSNVFNPATGAVQARVALAEPGTVDAAVASALAAFPAWSEQSSLR 67 G +L G +D + T +V NP+ G+V +VA A A+ A +A AW+ + Sbjct: 14 GIFLGGAFEDREET--FDVINPSDGSVLTKVASASQEDATRALDLATSAQGAWAATPARE 71 Query: 68 RSRVMFKFKELLDRHHDELAQIISREHGKVLSDAHGEVTRGIEIVEYACGAPNLLKTDFS 127 R ++ K ELL +L ++S E G+ L D+ EV G E + ++ D+ Sbjct: 72 RGEILRKTFELLIDATPDLTLLMSAELGRALPDSKSEVAYGAEFFRWFSEEAVRIRGDYR 131 Query: 128 DNIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERDPSASLL 187 + G +RQP+G +TP+NFP+ + I AL AG I+KP+ + P L Sbjct: 132 HSPAGNARIVEIRQPVGPSLAITPWNFPLAMGARKIAPALAAGCTIIVKPASKTPLTMLY 191 Query: 188 MARLLTEAGLPDGVFNVVQGDKVA-VDALLQHPDIEAISFVGSTPIAEYIHQQGTAHGKR 246 +A++L EAGLPDGV V+ K + + ALL P + +F GST + + + QG H + Sbjct: 192 LAKVLKEAGLPDGVLAVLPTSKSSRISALLDDPRLRKFTFTGSTEVGQSLAAQGAGHSLK 251 Query: 247 VQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDELIAKLLP 306 G +V+ DADL A DA++ A AG+ C+A + + + DE +A + Sbjct: 252 TSLELGGNAPYVVLEDADLPTAIDAMVTAKMRGAGQVCIAANRFLVHSSIKDEFVAGCVE 311 Query: 307 RIDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRSF-KVP-GAEQG 364 ++ Q ++GN GT +GPL + V +D + +GA + F ++P G E G Sbjct: 312 KLKQFRVGNATDEGTTVGPLSGEDQLEIVTDLVDDALEKGAT-----KHFGELPDGLEPG 366 Query: 365 FFVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCFTRDGGI 424 F+ ++ + AE +I EIFGPV+ + A+ L N FG F+ + Sbjct: 367 FYYPPSVLSDIPAEAAIASSEIFGPVIAVTTFDTDEEAIRLANNTPFGLAAYVFSENLTR 426 Query: 425 ARAFARSIKVGMVGINV-PIPVPMAWHSFGGWKRSLFG 461 A + A +I+ GMV +N + P A FGG K S G Sbjct: 427 ALSVAEAIEAGMVAVNKGALSDPAA--PFGGVKESGLG 462 Lambda K H 0.321 0.137 0.415 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: 483 Number of extensions: 16 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: 500 Length of database: 483 Length adjustment: 34 Effective length of query: 466 Effective length of database: 449 Effective search space: 209234 Effective search space used: 209234 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