Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_011426932.1 RHE_RS19035 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000092045.1:WP_011426932.1 Length = 502 Score = 366 bits (939), Expect = e-105 Identities = 206/482 (42%), Positives = 285/482 (59%), Gaps = 12/482 (2%) Query: 17 KIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWS 76 K++ +I GE+ + V G+ FE L+PV G L + D D N A++ A A + W Sbjct: 12 KLKYGNYIGGEWREPVEGKYFENLTPVTGGKLCDIPRSDEKDINLALDAAHAAKEN--WG 69 Query: 77 QLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAID 136 + + A+R L++ A + +E LA ET D GKPI ++ + DIP A + A I Sbjct: 70 RTSAAERSNILMKIAQRMEDRLELLAQAETWDNGKPIRETMAADIPLAIDHFRYFASCIR 129 Query: 137 KVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKS 196 + HD + EP+GVVG I+PWNFP+LMA WKL PALA GN VVLKP+E++ Sbjct: 130 AQEGSIGEIDHDTIAYHFHEPLGVVGQIIPWNFPILMATWKLAPALAAGNCVVLKPAEQT 189 Query: 197 PLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYA 256 P + + A+L + +P GVLN++ G+G GK LA + + FTG T + +M YA Sbjct: 190 PASILLWAELVGDL-LPPGVLNIVNGFGIEAGKPLATSPRIAKIAFTGETTTGRLIMQYA 248 Query: 257 GESNMKRIWLEAGGKSPNIVFADA----PDLQAAAEAAASAIAFNQGEVCTAGSRLLVER 312 + N+ + LE GGKSPNI FAD D A + A NQGEVCT SR LV+ Sbjct: 249 SQ-NLIPVTLELGGKSPNIFFADVMAEDDDFLDKALEGFAMFALNQGEVCTCPSRALVQE 307 Query: 313 SIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGK 372 SI D+F+ V+ ++ K GNPLDP T +GA T+Q+ +L+Y++ G ++GA++LAGG Sbjct: 308 SIYDRFMEKTVKRVEAIKQGNPLDPATMIGAQASTEQLEKILAYLDIGKQEGAQVLAGGS 367 Query: 373 RT---LEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGL 429 R + G YV+PTIF G N MRI QEEIFGPV+SV F T +EA+ IANDT YGL Sbjct: 368 RNDLGGDLANGYYVKPTIFKG-HNKMRIFQEEIFGPVVSVTTFKTEKEALEIANDTLYGL 426 Query: 430 AAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTE 489 AG+W+ D ++ ++ R ++AG VW N Y A FGG+KQSG GR+ LE Y + Sbjct: 427 GAGVWSRDANRCYRFGREIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRETHKMMLEHYQQ 486 Query: 490 LK 491 K Sbjct: 487 TK 488 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: 628 Number of extensions: 27 Number of successful extensions: 7 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: 502 Length adjustment: 34 Effective length of query: 463 Effective length of database: 468 Effective search space: 216684 Effective search space used: 216684 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