Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_035134835.1 Q763_RS12615 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000769915.1:WP_035134835.1 Length = 509 Score = 353 bits (907), Expect = e-102 Identities = 200/485 (41%), Positives = 282/485 (58%), Gaps = 14/485 (2%) Query: 15 QLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGV 74 Q K + FI G++ V GE F+ +SP+DG+ AK A D + A++ A F + Sbjct: 17 QFKEKYDNFIGGKFVPPVKGEYFDNISPIDGKPFAKAARSTKEDIDLALDAAHEAFKT-- 74 Query: 75 WSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEA 134 W + +PA R + L + AD++ N+E LA +ET+D GK I ++ + D+P + A Sbjct: 75 WGKASPAYRSSVLNKIADVMEANLEYLATVETIDNGKAIRETLAADLPLCIDHFRYFASV 134 Query: 135 IDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSE 194 I ++ + + +V EP+GVVG I+PWNFPLLMA WK+ PA+A GN V+K +E Sbjct: 135 IRGEEGTISEHDENTVSIVLHEPIGVVGQIIPWNFPLLMATWKIAPAIAAGNCTVVKAAE 194 Query: 195 KSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMV 254 ++P++ I + +L I+ +P GV+N++ G+G GK LA + + FTG T + +M Sbjct: 195 QTPVSIIVLMEL-IKDVVPPGVINIVNGFGVEAGKPLATSPRISKVSFTGETTTGRLIMQ 253 Query: 255 YAGESNMKRIWLEAGGKSPNIVF-----ADAPDLQAAAEAAASAIAFNQGEVCTAGSRLL 309 YA E N+ +E GGKSPNI F AD A E A A NQGE+CT SR+L Sbjct: 254 YAAE-NIIPSTMELGGKSPNIFFKSVGDADDEFFDKAVEGAVM-FALNQGEICTCPSRML 311 Query: 310 VERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLA 369 V I DKF+ V+ + K G+PLD +GA Q + SY++ G +GA++L Sbjct: 312 VHEDIYDKFIERVITRTEAIKIGHPLDKTVAMGAQASNDQYEKIKSYLKIGKDEGAQVLT 371 Query: 370 GGK-RTLEETGGT--YVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTP 426 GG+ L+ GT Y++PTIF G N MRI QEEIFGPV+ V F T EEA+ IANDT Sbjct: 372 GGEVNQLDGELGTGYYIQPTIFKG-NNKMRIFQEEIFGPVVCVTTFKTTEEAIEIANDTL 430 Query: 427 YGLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEK 486 YGL AG+WT D + ++ RA+ AG VWVN Y APFGG+K+SG GR+ LE Sbjct: 431 YGLGAGVWTRDAHELYQVPRAIEAGRVWVNNYHAYPAHAPFGGYKKSGFGRENHKMMLEH 490 Query: 487 YTELK 491 Y + K Sbjct: 491 YRQTK 495 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: 600 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: 509 Length adjustment: 34 Effective length of query: 463 Effective length of database: 475 Effective search space: 219925 Effective search space used: 219925 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