Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_090221318.1 CV091_RS15420 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_002796795.1:WP_090221318.1 Length = 504 Score = 316 bits (810), Expect = 1e-90 Identities = 184/478 (38%), Positives = 267/478 (55%), Gaps = 15/478 (3%) Query: 20 GRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVW-SQL 78 G AF+ G G P L + C A +A + A VW + Sbjct: 26 GGAFVTG------GGAKIALEDPFSRVILTEYPDCGAEIAKQACAASDAA--QKVWMADF 77 Query: 79 APAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKV 138 A R + + A+++ + E LA +E + GKPI D +++ ++ + A DK+ Sbjct: 78 TAAGRGIVMQKIANIVDERHETLAQVEAVVSGKPIRDCR-VEVAKVSEMFRYYAGYTDKL 136 Query: 139 YDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPL 198 + +V P P L REP+GV+ I PWN P+ A W++ PA+A GN VVLKPSE +P+ Sbjct: 137 HGQVIPVPSGHLNYTVREPLGVIFQITPWNAPMFTAGWQVAPAIACGNGVVLKPSELTPV 196 Query: 199 TAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGE 258 T+I +A + EAG P G++NVL G G T G+A H +VF GS + + AG+ Sbjct: 197 TSIALAAICEEAGAPKGLVNVLAGLGPTAGEAAIAHDATRKVVFVGSPATGRVVATSAGK 256 Query: 259 SNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKF 318 + +K + LE GGKS NIVF DA DL+AA + A +AI G+ C AGSRLLV+ SIKD+F Sbjct: 257 A-LKPVVLELGGKSANIVFEDA-DLEAACKGAQAAIFATAGQSCVAGSRLLVQASIKDQF 314 Query: 319 LPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEET 378 + MV + ++ K G+PLD T +G + + +Q + V + I KDGA +L G T E Sbjct: 315 VKMVADGMQQLKVGDPLDKATEIGPISNRRQFDHVTAMIGQAAKDGASVLTG---TSHEA 371 Query: 379 GGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDI 438 V PTI + AQ EIFGPV++V++F+ +A+ IAN T +GLA +WT ++ Sbjct: 372 DALIVPPTILADLPPGSDAAQTEIFGPVVTVLSFEDEADAIRIANSTDFGLAGAVWTKNV 431 Query: 439 SKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIK 496 S AH+ A VRAG+ WVN Y ++ PFGG + SG GR + L +YTE K+ W++ Sbjct: 432 SLAHRMAANVRAGTFWVNGYKAIHVSTPFGGSRSSGFGRSSGMDVLMEYTEPKSIWVE 489 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: 632 Number of extensions: 25 Number of successful extensions: 4 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: 504 Length adjustment: 34 Effective length of query: 463 Effective length of database: 470 Effective search space: 217610 Effective search space used: 217610 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