Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_015928270.1 MNOD_RS07620 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000022085.1:WP_015928270.1 Length = 506 Score = 377 bits (969), Expect = e-109 Identities = 217/477 (45%), Positives = 287/477 (60%), Gaps = 14/477 (2%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FI G++ G FE SP+ GR + +VA D D RA++ A A + W APA+ Sbjct: 22 FIGGQWVAPAGGRYFENTSPLTGRVICEVARSDAQDIERALDAAHAAKEA--WGHTAPAE 79 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L R AD + +N+E LAL ET D GKPI +++ DIP A + A I + Sbjct: 80 RARILNRMADRMEENLELLALAETWDNGKPIRETTHADIPLAIDHFRYFAGCIRAQEGSL 139 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 + D + EP+GVVG I+PWNFPLLMA WKL PALA GN VVLKP+E++P + + Sbjct: 140 SEIDQDTVAYHFHEPLGVVGQIIPWNFPLLMAVWKLAPALAAGNCVVLKPAEQTPASVLV 199 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMK 262 +A++ + +PAGVLN++ G+G GK LA + + FTG T + +M YA + N+ Sbjct: 200 LAEIVGDL-LPAGVLNIVNGFGLEAGKPLASSPRIAKIAFTGETSTGRLIMQYASQ-NLI 257 Query: 263 RIWLEAGGKSPNIVFAD--APD---LQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDK 317 + LE GGKSPNI F D A D L A E + A NQGEVCT SR LV +I D+ Sbjct: 258 PVTLELGGKSPNIFFKDVLAEDDAFLDKALE-GFTMFALNQGEVCTCPSRALVHEAIYDR 316 Query: 318 FLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTL-- 375 F+ V + K G+PLDP T +GA +Q+ +LSYI+ G ++GA+LL GG+R Sbjct: 317 FIEKAVARVNAIKQGSPLDPATMIGAQASGEQLQKILSYIDIGKQEGAQLLTGGERNRLE 376 Query: 376 -EETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIW 434 E G YV+PT+F G N MRI QEEIFGPVLSV F EEA+AIANDT YGL AG+W Sbjct: 377 GEFAQGFYVKPTVFKG-HNRMRIFQEEIFGPVLSVTTFKDDEEALAIANDTLYGLGAGVW 435 Query: 435 TSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 T DI++A++ RA++AG VW N Y A FGG+KQSG GR+ L+ Y + K Sbjct: 436 TRDITRAYRFGRAIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRENHRMMLDHYQQTK 492 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: 645 Number of extensions: 29 Number of successful extensions: 6 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: 506 Length adjustment: 34 Effective length of query: 463 Effective length of database: 472 Effective search space: 218536 Effective search space used: 218536 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 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