Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_009762358.1 MICLODRAFT_RS03140 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000262405.1:WP_009762358.1 Length = 496 Score = 455 bits (1171), Expect = e-132 Identities = 234/478 (48%), Positives = 315/478 (65%) Query: 20 GRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLA 79 G FI+ + A SGE +SP+DG L +A+ D D NRAV AR +F +G WS +A Sbjct: 19 GLNFIDNKAVSAASGEVMPVISPIDGTQLTVLAASDSEDMNRAVAAARRSFETGCWSGMA 78 Query: 80 PAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVY 139 P +RK ++++ADL+ ++ E+A+L D G I + + AA I + AEAIDK Sbjct: 79 PRERKRIMLKWADLIDRHALEIAVLGVRDNGTDIRMALKGEPQSAADTIRFYAEAIDKRN 138 Query: 140 DEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLT 199 E+ PT HD L L+ RE VGVVG I+PWNFPL++ WKL PALA GNSVV+KPSE++ L+ Sbjct: 139 GEITPTRHDILSLIHREAVGVVGVIIPWNFPLMIGSWKLAPALAAGNSVVVKPSEEASLS 198 Query: 200 AIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGES 259 +R+ +LA EAGIP GVLN + G G VG+AL LHMDVD L FTGS + ++L+ Y+ S Sbjct: 199 ILRVIELAAEAGIPPGVLNAVNGRGAIVGEALGLHMDVDVLGFTGSGGVGRRLLEYSARS 258 Query: 260 NMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFL 319 N+KR++LE GGKSPN+VFADAP+L+ AA A++I N G+VC A SRL VERS+ F+ Sbjct: 259 NLKRVYLELGGKSPNLVFADAPNLKRAARETAASIFRNNGQVCAAASRLAVERSVYKDFM 318 Query: 320 PMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETG 379 V + G+PL T GAL + Q+ + I + GA + GG + E+G Sbjct: 319 EAVRAEATAMRIGDPLSLAFTTGALANAAQLAKTRAAIARAAEQGATVYHGGNQLHAESG 378 Query: 380 GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDIS 439 G Y EPTI V M + Q+EIFGPVL +FDT EEA+AIAN+T +GL++ +WT D+S Sbjct: 379 GFYHEPTILTDVATEMDVVQQEIFGPVLVARSFDTEEEAIAIANETVFGLSSVLWTRDLS 438 Query: 440 KAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIKL 497 KAH+ + +++G V +N Y G D+TAP GG +QSGNG D+SLHALEKY LK WI+L Sbjct: 439 KAHRVSNRIKSGVVHINCYSGADITAPLGGVRQSGNGSDRSLHALEKYENLKTKWIQL 496 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: 590 Number of extensions: 18 Number of successful extensions: 1 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: 496 Length adjustment: 34 Effective length of query: 463 Effective length of database: 462 Effective search space: 213906 Effective search space used: 213906 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