Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_085634733.1 MGEO_RS00465 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_002115805.1:WP_085634733.1 Length = 508 Score = 344 bits (883), Expect = 4e-99 Identities = 186/480 (38%), Positives = 286/480 (59%), Gaps = 7/480 (1%) Query: 20 GRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLA 79 GR I+G + ETF+ +SP G ++ + + + A++ AR F++G+WS+++ Sbjct: 20 GRHLIDGAWV--TGRETFDRVSPSHGTVVSTSSKGGPEETDAAIKAARRAFDAGIWSRIS 77 Query: 80 PAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAE-AIDKV 138 +R A L+R ADL+ NV+ +AL ETL+ GKPI S ++ GAA + A A Sbjct: 78 GRERAAVLLRVADLIEANVDRIALQETLESGKPISQSKG-EVAGAADLWRYAAALARTSQ 136 Query: 139 YDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPL 198 D D LG+V ++P+GVV I PWNFP + KL ALA G +VV+KPSE +P Sbjct: 137 GDSHNTLGSDMLGVVVKDPIGVVSVITPWNFPFWILSQKLPFALAAGCTVVVKPSEMTPS 196 Query: 199 TAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGE 258 + + + +L ++AG+PAGV N++ GYG VG + H DVD + FTGST + K L+ A Sbjct: 197 STVMMGELLMQAGLPAGVCNIVLGYGDPVGSLKSTHPDVDMVTFTGSTAVGK-LITKAAS 255 Query: 259 SNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKF 318 +K++ LE GGK+P ++F DA DL+ AA+A + FN G+ C + SR++V I + F Sbjct: 256 DTLKKVALELGGKNPQVIFPDA-DLENAADAVTFGVYFNVGQCCNSSSRIIVHEDIAEDF 314 Query: 319 LPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKL-LAGGKRTLEE 377 + VV K K G+PLDP T VGA+V + + Y++ GA+L L G +E Sbjct: 315 VARVVALSKKVKFGDPLDPTTQVGAIVTPEHNARIDGYVQEAVAAGARLELGGAYLDVEG 374 Query: 378 TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSD 437 G + +PT+ V+ M +A+EE+FGPVLSV+ F T ++A+A+ ND+ YGL+AG+W+ Sbjct: 375 LGDQFYQPTVISSVSADMAVAREEVFGPVLSVLTFRTLDDAIALTNDSEYGLSAGVWSES 434 Query: 438 ISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIKL 497 + + AR +AG+VW N + G FGG KQSG GR+ + E++ E+K+ +++ Sbjct: 435 VHTCLEFARRAQAGTVWTNTWMDGYPELAFGGMKQSGTGREIGKYGFEEFLEVKSVVMRV 494 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: 656 Number of extensions: 37 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: 508 Length adjustment: 34 Effective length of query: 463 Effective length of database: 474 Effective search space: 219462 Effective search space used: 219462 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