Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19); betaine-aldehyde dehydrogenase (EC 1.2.1.8) (characterized)
to candidate WP_053938969.1 WG78_RS16670 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::Q9STS1 (503 letters) >NCBI__GCF_001294205.1:WP_053938969.1 Length = 466 Score = 315 bits (806), Expect = 3e-90 Identities = 174/464 (37%), Positives = 262/464 (56%), Gaps = 10/464 (2%) Query: 7 RRQLFIGGQWTEPVLRKTLPVVNPATEDIIGYIPAATSEDVELAVEAARKAFTRNNGKDW 66 R+Q F+ G W + ++T+PV NPAT +II +IP + A+EAA+ A+ W Sbjct: 10 RQQCFVNGAWIDADNQETVPVNNPATGEIIAHIPKLGKAETRRAIEAAQAAWPA-----W 64 Query: 67 ARATGAVRAKYLRAIAAKVIERKSELANLEAIDCGKPLDEAAWDMDDVAGCFEYYADLAE 126 T R++ LR ++ +LA + + GKPL EA ++ A E++A+ A Sbjct: 65 RSKTAKERSQILRKWNDLMLANVDDLALILTSEQGKPLAEARGEITYAASYIEWFAEEAR 124 Query: 127 GLDAKQKTPLSLPMDTFKGYILKEPIGVVGMITPWNYPLLMAVWKVAPSLAAGCTAILKP 186 ++ P P + + +LK+PIGV ITPWN+P M KV P+LAAGC +LKP Sbjct: 125 RIEGDIIAP---PSNDRRILVLKQPIGVTAAITPWNFPAAMITRKVGPALAAGCPMVLKP 181 Query: 187 SELASLTCLELADICREVGLPPGVLNILTGLGTEAGAPLASHPHVDKIVFTGSTTTGSSI 246 + L+ L LA + G+P G+ N+LTG TE G L + P V KI FTGST G+ + Sbjct: 182 ATQTPLSALALAVLAERAGVPAGIFNVLTGSSTEIGGELTASPIVRKITFTGSTEVGAKL 241 Query: 247 MTSAAKLVKPVSLELGGKSPIIVFDDVDIDKAVEWTMFGCFWTNGQICSATSRLLVHERI 306 + +A +K +S+ELGG +P IVFDD D+D AV+ + + +GQ C +RLLV + Sbjct: 242 IEQSAPTIKKMSMELGGNAPFIVFDDADLDAAVQGAIGSKYRNSGQTCVCANRLLVQAGV 301 Query: 307 ADEFLDKLVKWTKNIKISDPFEEGCRLGPVVSKGQYERVLKFVSNARNEGATVLCGGVRP 366 D F KL +K+ + ++G GP++ ++ + +++A +GA VL GG R Sbjct: 302 YDAFAQKLADAVNALKVGNGVDDGVTQGPLIDDKAIAKIEEHIADATGKGAQVLTGGKR- 360 Query: 367 EHLKKGYFVEPAIVSNVTTSMEIWREEVFGPALCVKTFSTEDEAIQLANDSQYGLAGAVL 426 H G F EP I++ VT +M++ REE FGP + F TE+EAI +AND+++GLA Sbjct: 361 -HALGGTFFEPTILTGVTPAMKVAREETFGPLAPLFKFETEEEAIAMANDTEFGLASYFY 419 Query: 427 SNDLERCDRVSKAFQAGIVWVNCSQPCFCQAPWGGTKRSGFGRE 470 + DL R RV++ + G+V +N AP+GG K+SG GRE Sbjct: 420 TRDLARIFRVAEGLEYGMVGINAGLISSEVAPFGGVKQSGLGRE 463 Lambda K H 0.318 0.135 0.421 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: 570 Number of extensions: 26 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: 466 Length adjustment: 34 Effective length of query: 469 Effective length of database: 432 Effective search space: 202608 Effective search space used: 202608 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 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