Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_073950325.1 RH94_RS25575 gamma-aminobutyraldehyde dehydrogenase
Query= reanno::WCS417:GFF5420 (497 letters) >NCBI__GCF_001906585.1:WP_073950325.1 Length = 511 Score = 329 bits (843), Expect = 2e-94 Identities = 183/475 (38%), Positives = 265/475 (55%), Gaps = 7/475 (1%) Query: 19 EGRAYINGEYTAAVSGDTFECISPVDGRLLATVASCDAADAQRAVENARATFNSGVWSRL 78 +G YI G T SG T + P G + T D AV AR F W+ Sbjct: 20 DGAQYIAGRLTKGTSGRTHAVVDPATGEEVHTYELAGPDDVDAAVAAAREAFPG--WAGA 77 Query: 79 APAKRKSAMLRFAALLKANAEELALLETLDMGKPISDSLNIDVPGAA-NALSWSGEAIDK 137 P R A+ RFA +L AE+ A E+L GKP+ + DVPG NA ++G A Sbjct: 78 TPGDRSDALHRFAEVLADRAEDFARAESLQCGKPLKLTREFDVPGTIDNAAFFAGAARHL 137 Query: 138 IYDEVAATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGPALSTGNSVILKPSEKSP 197 D V REP+GVVG+I PWN+PL MA WK+ PA++ GN+++LKP+E +P Sbjct: 138 QGQSAGEYSGDHTSYVRREPIGVVGSIAPWNYPLQMAAWKVLPAIAAGNTIVLKPAELTP 197 Query: 198 LTAIRIAALAVEAGIPKGVFNVLPGYGHTVGNALALHMDVDTLVFTGSTKIAKQLLIRSG 257 LT++ A A EAGIP GV N++ G G G L H DV + FTGST + K++ Sbjct: 198 LTSLLFAQAATEAGIPDGVINIVTGTGKEAGEHLVGHPDVAMVSFTGSTAVGKRVA-EIA 256 Query: 258 ESNMKRVWLEAGGKSPNIVFADAPDLQAAAESAAGAIAFNQGEVCTAGSRLLVERSIKDK 317 +++KR+ LE GGK+P +VF DA DL+AA A N G+ CTA +R V+R + ++ Sbjct: 257 TASVKRLHLELGGKAPFVVFDDA-DLEAAVNGAVAGALINTGQDCTAATRAYVQRPLYEE 315 Query: 318 FLPLVIEALKGWKPGNPLDPATNVGALVDTQQMNTVLSYIEAGHADGAKLVAGGKRTLEE 377 F+ ++ + G+P P T++G L+ + V +++ A A++V GG+ E Sbjct: 316 FVARTAALMETVRLGDPFAPGTDLGPLISHVHRDRVAGFVDRARAY-ARVVTGGEAPQGE 374 Query: 378 T-GGTYVEPTIFDGVTNAMKIAKEEIFGPVLSVITFDSAEEAVAIANDTIYGLAAAVWTA 436 G Y PT+ G +I + EIFGPVL V+ FDS +E + +ANDT YGLAA+ W+ Sbjct: 375 LKNGAYYRPTLIAGAAQDSEIVQSEIFGPVLVVLPFDSDDEGIRLANDTAYGLAASAWSR 434 Query: 437 DISKAHLTAKALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHAFDKYTELK 491 D+ +A+ + ++AG VWVN + P GG KQSG G+D S ++F++YT++K Sbjct: 435 DVYRANRATREIKAGCVWVNDHIPIISEMPHGGSKQSGFGKDMSSYSFEEYTQIK 489 Lambda K H 0.316 0.132 0.386 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: 680 Number of extensions: 31 Number of successful extensions: 4 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: 497 Length of database: 511 Length adjustment: 34 Effective length of query: 463 Effective length of database: 477 Effective search space: 220851 Effective search space used: 220851 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 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