Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_068166964.1 HTA01S_RS02495 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_001592305.1:WP_068166964.1 Length = 494 Score = 370 bits (951), Expect = e-107 Identities = 199/480 (41%), Positives = 277/480 (57%), Gaps = 3/480 (0%) Query: 14 QQLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSG 73 + + ++ FI G + L P DG+ A + D + + AV+NA + Sbjct: 7 RSIAVQSAHFIGGRVVPDTA--LLNVLRPSDGQVHAGLPLADASTVDAAVQNAWQAWRHT 64 Query: 74 VWSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAE 133 W++ AP +R L R+ADL+ E LA LE + +P+ D+++ D+P A+ + + +E Sbjct: 65 DWARRAPRERARVLRRWADLIEAEGERLAQLEAVCSTRPVRDAAAWDVPFTAEGLRFFSE 124 Query: 134 AIDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPS 193 DK+ EVA T HD LGLV EP GVVGAI PWNFPL+M WK+G ALA GN+VVLKPS Sbjct: 125 YADKLGGEVAATRHDHLGLVVAEPYGVVGAITPWNFPLVMVSWKVGAALAAGNAVVLKPS 184 Query: 194 EKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLM 253 E +P + IR+A+LAIEAG+PAG+ N++ G G T G AL H + + FTGST+ +M Sbjct: 185 EMTPFSVIRLAELAIEAGVPAGIFNIVQGDGRTTGDALTRHPLISKMTFTGSTRTGAAIM 244 Query: 254 VYAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERS 313 K + LE GGKSP +VF D PD+ A A AI N G+VC AGSRL+V+R Sbjct: 245 ASCALQGPKPVTLELGGKSPQLVFDDVPDVDRVAGIVARAITGNAGQVCVAGSRLIVQRG 304 Query: 314 IKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKR 373 + + + + + KPG D Q T+ ++ QQ +L +E GA+L GG Sbjct: 305 VAEALIDGIAQRFGALKPGATWDGQATLPPIISAQQAARMLDIVERARDAGAQLRCGGGL 364 Query: 374 TLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGI 433 GG Y +PT+ +GVT QEEIFGPVL+V FDT EE +A+A YGLAAG+ Sbjct: 365 FDGGPGGAYFQPTLIEGVTADNPAVQEEIFGPVLTVQTFDTEEEGLALAAHEHYGLAAGV 424 Query: 434 WTSDISKAHKTARAVRAGSVWVNQYD-GGDMTAPFGGFKQSGNGRDKSLHALEKYTELKA 492 T+DI +A + R + AG+VW+N+Y D P GG+ QSG G+D A+E K+ Sbjct: 425 HTADIGRAMRAMRGLSAGTVWINRYGRSDDFVIPTGGYHQSGIGKDLGRQAVEANLRFKS 484 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: 710 Number of extensions: 28 Number of successful extensions: 2 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: 494 Length adjustment: 34 Effective length of query: 463 Effective length of database: 460 Effective search space: 212980 Effective search space used: 212980 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