Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_058931030.1 AU252_RS12650 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_001484605.1:WP_058931030.1 Length = 507 Score = 348 bits (894), Expect = e-100 Identities = 201/484 (41%), Positives = 284/484 (58%), Gaps = 12/484 (2%) Query: 15 QLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGV 74 Q K +I GE+ +G+ E +SPV+G+ +VA AD A++ A + Sbjct: 15 QFKDRYENWIGGEWVAPTTGQYIENVSPVNGKQFTEVARGAAADVELALDAAHKA--APA 72 Query: 75 WSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEA 134 W + + +R A L + AD + N+E LA+ E+ D GKPI ++ + DIP AA + A A Sbjct: 73 WGKASATERAAVLNKIADRIDANLEMLAVAESWDNGKPIRETLNADIPLAADHFRYFASA 132 Query: 135 IDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSE 194 I ++ D EP+GVVG I+PWNFP+LMA WK+ PALA GN+VVLKP+ Sbjct: 133 IRAQEGRLSQLDDDTTAYHFHEPLGVVGQIIPWNFPILMAVWKMAPALAAGNAVVLKPAS 192 Query: 195 KSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMV 254 +P + + +A+L + +PAG+LN++ G+G VGK LA + + FTG T + + Sbjct: 193 NTPASILVLAELIADL-LPAGLLNIVNGFGAEVGKPLASSPRIRKIAFTGETSTGRLISQ 251 Query: 255 YAGESNMKRIWLEAGGKSPNIVFADAPDLQAA----AEAAASAIAFNQGEVCTAGSRLLV 310 YA + N+ + LE GGKSPNI F D + A A + AFNQGEVC++ SR LV Sbjct: 252 YASQ-NLIPVTLELGGKSPNIFFNDVAESNDAFYDKALEGFTLYAFNQGEVCSSPSRALV 310 Query: 311 ERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAG 370 + I D F+ V + GNPLD T +GA QM +LSYI+ G ++GA +L+G Sbjct: 311 QDGIYDSFMADAVARTEQIIQGNPLDTNTQIGAQASVGQMEKILSYIDIGLEEGATILSG 370 Query: 371 GKRTL---EETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPY 427 G RT + GG YV+PTIF+G N+MRI QEEIFGPV+SV F ++AV+IANDT Y Sbjct: 371 GARTELDGDLAGGYYVQPTIFEG-QNSMRIFQEEIFGPVVSVARFGDYKDAVSIANDTLY 429 Query: 428 GLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKY 487 GL AG+W+ + + A++ R ++AG VWVN Y A FGG+K SG GR+ L+ Y Sbjct: 430 GLGAGVWSRNGNVAYRAGREIQAGRVWVNNYHAYPAGAAFGGYKSSGIGRENHSMMLDHY 489 Query: 488 TELK 491 + K Sbjct: 490 QQTK 493 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: 655 Number of extensions: 43 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: 507 Length adjustment: 34 Effective length of query: 463 Effective length of database: 473 Effective search space: 218999 Effective search space used: 218999 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