Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_046158953.1 VL52_RS21455 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000971335.1:WP_046158953.1 Length = 500 Score = 348 bits (894), Expect = e-100 Identities = 203/484 (41%), Positives = 276/484 (57%), Gaps = 12/484 (2%) Query: 15 QLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGV 74 +LK +I G + V+G FE ++P+ G+ L ++ D D A++ A A + Sbjct: 8 ELKSRYANYIGGRWVPPVNGRYFENVTPITGQPLCEIPRSDEQDVELALDAAHAARYA-- 65 Query: 75 WSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEA 134 W +R L R AD + N+ LA +ET D GKPI ++ + DIP A + A Sbjct: 66 WGHTPVTERAIVLNRIADRMEANLALLAEVETWDNGKPIRETRAADIPLAIDHFRYFASC 125 Query: 135 IDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSE 194 + + + + EP+GVVG I+PWNFP+LMA WKL PALA GN VVLKP+E Sbjct: 126 VRAQEGSLGEIDANTVSYHFHEPLGVVGQIIPWNFPILMAAWKLAPALAAGNCVVLKPAE 185 Query: 195 KSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMV 254 ++PL+ + + +L + +P GVLNV+ G+G GK LA + + FTG T + +M Sbjct: 186 QTPLSILVLMELVGDL-LPPGVLNVVNGFGVEAGKPLASSKRIAKIAFTGETGTGRLIMQ 244 Query: 255 YAGESNMKRIWLEAGGKSPNIVFAD--APDLQAAAEAAASAIAF--NQGEVCTAGSRLLV 310 YA + N+ + LE GGKSPNI F D A D +A + F NQGEVCT SR L+ Sbjct: 245 YASQ-NLIPVTLELGGKSPNIFFGDVAAKDDAFLDKAIEGFVMFALNQGEVCTCPSRALI 303 Query: 311 ERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAG 370 SI D+F+ + + K GNPLDP T +GA +QM+ + SY+ G +GAKLLAG Sbjct: 304 HESIYDRFMEKALARVAAIKQGNPLDPATMIGAQASQEQMDKIQSYLAIGRDEGAKLLAG 363 Query: 371 GKRTLEE---TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPY 427 G R + GG Y++PT+F G N MRI QEEIFGPV+SV F +EA+AIANDT Y Sbjct: 364 GGRAQLDGDLAGGFYIQPTVFHG-HNKMRIFQEEIFGPVVSVTTFKDRDEALAIANDTLY 422 Query: 428 GLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKY 487 GL AG+WT D++ A R + AG VW N Y A FGG+KQSG GR+ LE Y Sbjct: 423 GLGAGVWTRDMNTAFFMGRHIEAGRVWTNCYHAYPAHAAFGGYKQSGIGRETHKMMLEHY 482 Query: 488 TELK 491 + K Sbjct: 483 QQTK 486 Lambda K H 0.316 0.132 0.390 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: 633 Number of extensions: 37 Number of successful extensions: 8 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: 500 Length adjustment: 34 Effective length of query: 463 Effective length of database: 466 Effective search space: 215758 Effective search space used: 215758 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