Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate BWI76_RS21985 BWI76_RS21985 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >FitnessBrowser__Koxy:BWI76_RS21985 Length = 506 Score = 337 bits (863), Expect = 8e-97 Identities = 191/477 (40%), Positives = 273/477 (57%), Gaps = 14/477 (2%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FI+G++ + + GE F SPVDG + + D D + A++ A ++ W + + Sbjct: 22 FIDGKFVEPIGGEFFMNTSPVDGSNIGQFPRSDAKDIDFALDAAHRAADA--WGKTSAQH 79 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L++ AD + N+E LA+ E+ D GKPI ++ + D+P A + A + Sbjct: 80 RANLLLQVADRIEANLEYLAVAESWDNGKPIRETLNADLPLAVDHFRYFAGCLRAQEGST 139 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 A + EP+GVVG I+PWNFPLLMA WKL PALA GN VVLKP+E++PL+ Sbjct: 140 AEIDETTVAYHFHEPLGVVGQIIPWNFPLLMAAWKLAPALAAGNCVVLKPAEQTPLSITL 199 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMK 262 + ++ I PAGVLNV+ G+G G+ALA + + FTGST + + +M A E N+ Sbjct: 200 LLEI-IGDLFPAGVLNVVQGFGKEAGEALATSKRIAKIAFTGSTPVGRHIMACAAE-NII 257 Query: 263 RIWLEAGGKSPNIVFADAPD-----LQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDK 317 +E GGKSPNI FAD + ++ A E FNQGEVCT SR L++ SI + Sbjct: 258 PCTVELGGKSPNIYFADVMEGEEEYIEKAVEGLVLGF-FNQGEVCTCPSRALIQESIYEP 316 Query: 318 FLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKR---T 374 F+ V++ + + G+P D T +GA QQ + +LSYI+ +G K+L GG+R + Sbjct: 317 FMARVMDKVAQIRRGDPFDTDTMIGAQASRQQFDKILSYIKIARDEGGKILTGGERASIS 376 Query: 375 LEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIW 434 E G Y++PT+ G N MR QEEIFGPV+ V F EA++IAN T +GL AG+W Sbjct: 377 AELDNGFYIQPTLIQG-RNDMRSFQEEIFGPVIGVTTFKDEAEALSIANQTQFGLGAGVW 435 Query: 435 TSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 T D + A++ R ++AG VW N Y A FGG+KQSG GR+ AL Y + K Sbjct: 436 TRDTNLAYRMGRGIKAGRVWTNCYHIYPAHAAFGGYKQSGVGRETHKMALNAYQQTK 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: 654 Number of extensions: 39 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