Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate GFF3202 HP15_3144 NAD-dependent aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >FitnessBrowser__Marino:GFF3202 Length = 533 Score = 348 bits (893), Expect = e-100 Identities = 192/476 (40%), Positives = 279/476 (58%), Gaps = 12/476 (2%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 +I GE+ V G+ FE ++PV G + ++ D + A++ A + W + +P + Sbjct: 49 YIGGEWVAPVKGQYFENITPVTGNVICEIPRSSAEDIDLALDAAHKA--APAWGKTSPTE 106 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L++ AD + N+E+LA+ ET D GK + ++ + DIP AA + A + + Sbjct: 107 RSNILLKIADRIEANLEKLAVAETWDNGKAVRETLNADIPLAADHFRYFAGCLRAQEGHM 166 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 H+ + EP+GVVG I+PWNFP+LMA WKLGP LA GN VLKP+E++P + + Sbjct: 167 GEIDHNTVAYHFHEPLGVVGQIIPWNFPILMAAWKLGPCLAAGNCTVLKPAEQTPASILV 226 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMK 262 + ++ I +P GVLN++ GYG G+ALA + + FTGST + ++ A E N+ Sbjct: 227 LMEI-IGDLLPPGVLNIVNGYGIEAGQALATSKRIAKIAFTGSTPVGSHILKCAAE-NII 284 Query: 263 RIWLEAGGKSPNIVFADA----PDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKF 318 +E GGKSPNI F+D P+ FNQGEVCT SR LV+ + ++F Sbjct: 285 PSTVELGGKSPNIYFSDVMKAEPEFIDKCVEGLVLAFFNQGEVCTCPSRALVQEDMFEEF 344 Query: 319 LPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRT-LEE 377 + VV+ K K GNPLD VGA +Q + ++SY+ G ++GA +L GG R L+E Sbjct: 345 MQKVVQRTKSIKRGNPLDTDVQVGAQASKEQFDKIMSYLAIGKEEGAVVLTGGDREHLDE 404 Query: 378 --TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWT 435 G Y++PT+F G N MR+ QEEIFGPV+ V F T EEA+AIANDT +GL AG+WT Sbjct: 405 EFNNGFYIQPTLFKG-DNKMRVFQEEIFGPVVGVTTFKTEEEALAIANDTEFGLGAGVWT 463 Query: 436 SDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 D + A++ R ++AG VW+N Y A FGG+K+SG GR+ ALE Y + K Sbjct: 464 RDTNLAYRMGRNIQAGRVWMNCYHAYPAHAAFGGYKKSGVGRETHKMALEHYQQTK 519 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: 674 Number of extensions: 34 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: 533 Length adjustment: 35 Effective length of query: 462 Effective length of database: 498 Effective search space: 230076 Effective search space used: 230076 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