Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate Dsui_1464 Dsui_1464 NAD-dependent aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >FitnessBrowser__PS:Dsui_1464 Length = 506 Score = 347 bits (890), Expect = e-100 Identities = 194/484 (40%), Positives = 277/484 (57%), Gaps = 12/484 (2%) Query: 15 QLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGV 74 Q K FI G++ V G+ F+ ++P+ G+ + A D A++ A A + Sbjct: 14 QYKARYDNFIGGKWVAPVKGQYFDVITPITGKPYTQAAQSGAEDIELALDAAHAAADK-- 71 Query: 75 WSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEA 134 W + + +R L++ AD + N+E LA +ET+D GK I ++ + DIP AA + A Sbjct: 72 WGKTSATERSNILLKIADRIEANLEMLAYVETVDNGKAIRETLNADIPLAADHFRYFAGC 131 Query: 135 IDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSE 194 + ++ + + EP+GVVG I+PWNFP+LMA WKL PAL GN VVLKP+E Sbjct: 132 LRSQEGSISEIDENTIAYHFHEPLGVVGQIIPWNFPILMAAWKLAPALGAGNCVVLKPAE 191 Query: 195 KSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMV 254 +P++ + +A+L + +P GVLN++ GYG G ALA + + FTGST + ++ Sbjct: 192 STPISILVLAELIADL-LPPGVLNIVNGYGRDAGMALASSKRIAKIAFTGSTATGR-VIA 249 Query: 255 YAGESNMKRIWLEAGGKSPNIVFADA----PDLQAAAEAAASAIAFNQGEVCTAGSRLLV 310 A +++ LE GGKSPNI FAD D A AFNQGEVCT SR L+ Sbjct: 250 QAAANSLIPATLELGGKSPNIFFADVAAADDDFFDKAIEGLVLFAFNQGEVCTCPSRALI 309 Query: 311 ERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAG 370 SI D F+ V+ +K K G+PLD + +GA QM+ ++SY+ G ++GA+ L G Sbjct: 310 HESIYDHFMERVLARVKAIKQGSPLDTDSMMGAQASQMQMDKIMSYLAIGKEEGAQCLVG 369 Query: 371 GKRTL---EETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPY 427 G R E G Y++PT+F G N MRI QEEIFGPVL+V F T EA+ IANDTPY Sbjct: 370 GDRARLGGELAEGYYIQPTLFKG-HNKMRIFQEEIFGPVLAVTTFKTEAEALEIANDTPY 428 Query: 428 GLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKY 487 GL AG+W+ D + A++ R ++AG VW N Y A FGG+K+SG GR+ L+ Y Sbjct: 429 GLGAGVWSRDGNTAYRMGRGIKAGRVWTNCYHAYPAHATFGGYKESGIGRETHKMMLDHY 488 Query: 488 TELK 491 + K Sbjct: 489 QQTK 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: 629 Number of extensions: 35 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 Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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