Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_099618760.1 CLH62_RS14090 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_002744735.1:WP_099618760.1 Length = 506 Score = 346 bits (887), Expect = 1e-99 Identities = 192/478 (40%), Positives = 280/478 (58%), Gaps = 16/478 (3%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FI GE+ V G+ FE ++PV G + ++ D + A++ A + W + + + Sbjct: 22 FIGGEWVAPVKGQYFENITPVTGDVICEIPRSGAEDIDLALDAAHKA--APAWGKTSTTE 79 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L++ AD + +N+E LA+ ET D GK + ++ + D+P A + A I D Sbjct: 80 RSNILLKIADRIEQNIEMLAVAETWDNGKAVRETINADLPLAVDHFRYFAGCIRAQEDTS 139 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 + ++ + EP+GVVG I+PWNFPLLMA WKL P LA GN V+KP+E++P + + Sbjct: 140 SAIDNNTVAYHYHEPLGVVGQIIPWNFPLLMAVWKLAPCLAAGNCTVMKPAEQTPASILV 199 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMK 262 + +L + +P GV+N++ GYG G+ALA + + FTGST + ++ A E N+ Sbjct: 200 LMELIGDL-LPPGVINIVNGYGIEAGQALATSKRIAKIAFTGSTPVGSHILKCAAE-NII 257 Query: 263 RIWLEAGGKSPNIVFADAPDLQAAAEAAASAIA------FNQGEVCTAGSRLLVERSIKD 316 +E GGKSPNI F+D +QA E + FNQGEVCT SR L++ + D Sbjct: 258 PSTVELGGKSPNIYFSDV--MQAEPEFIDKCVEGLVLAFFNQGEVCTCPSRALIQEDMYD 315 Query: 317 KFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLE 376 +F+ VVE K K GNPLD VGA +Q + ++SY+E G ++GA++L GG R Sbjct: 316 EFMAKVVERTKAIKRGNPLDTDVQVGAQASKEQFDKIMSYLEIGKQEGAEVLTGGGREEM 375 Query: 377 E---TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGI 433 E G YV+PT+ G N MR+ QEEIFGPV+ V F EEA+AIANDT +GL AG+ Sbjct: 376 EGQYNNGFYVQPTLLKG-RNDMRVFQEEIFGPVVGVTTFKDEEEALAIANDTEFGLGAGL 434 Query: 434 WTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 WT DI++A++ RA++AG VW N Y A FGG+K+SG GR+ AL+ Y + K Sbjct: 435 WTRDINRAYRMGRAIQAGRVWTNCYHQYPAHAAFGGYKKSGVGRENHKMALDHYQQTK 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: 649 Number of extensions: 31 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 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