Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_043532311.1 JH15_RS16505 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000759345.1:WP_043532311.1 Length = 487 Score = 298 bits (764), Expect = 2e-85 Identities = 175/478 (36%), Positives = 271/478 (56%), Gaps = 9/478 (1%) Query: 22 AFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPA 81 A+I+G + A SGE + +P +G + +V A+ RA+ A A F + W Sbjct: 14 AYIDGSWVAADSGEQIDVFNPANGEVIGRVPRLGRAETERAITAADAAFPA--WRAHTAQ 71 Query: 82 KRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDE 141 +R L+++ DL+ ++ EELA + TL+ GKP+ +++ +I AA + W AE ++Y E Sbjct: 72 ERADILMKWHDLMHEHQEELATIMTLEQGKPLKEAAG-EIAYAASFLRWFAEEARRMYGE 130 Query: 142 VAPTPH-DQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTA 200 P +Q ++T++PVGVVGAI PWNFP M K+G ALA G +V+KP+ ++P +A Sbjct: 131 TIPAAKPNQRIVITKQPVGVVGAITPWNFPAAMITRKVGAALAAGCPIVVKPASQTPFSA 190 Query: 201 IRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESN 260 +A LA AG+P GV NV+ G + AL +V + FTGST++ +QLM A + + Sbjct: 191 TALALLAERAGVPRGVFNVVTGSAREIAAALTESPEVRKITFTGSTEVGRQLMSQASQ-H 249 Query: 261 MKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLP 320 +++I LE GG +P IVF DA DL AA + A +A N G+ C +R LV+ S+ + F Sbjct: 250 IQKISLELGGNAPFIVFEDA-DLDAAVDGAMAAKFRNGGQTCVCTNRFLVQSSVVNAFCE 308 Query: 321 MVVEALKG-WKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETG 379 + A+ + G+ L +G L+D + V +++ GA+LL GG G Sbjct: 309 KLAVAMNSELRVGDGLKDDVNIGPLIDADGVEKVSAHVHDAVDKGAELLLGGNP--HPLG 366 Query: 380 GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDIS 439 G + PT+ +G M +AQEE FGP+ +V FD E+AVA+ANDT +GLA+ ++ D++ Sbjct: 367 GNFFTPTLVNGANADMLVAQEETFGPLAAVFPFDDEEDAVAMANDTQFGLASYFYSRDLA 426 Query: 440 KAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIKL 497 + + A ++ G V +N + APFGG K SG GR+ LE++ E K I L Sbjct: 427 RVWRVAESLEYGMVGINTGLISNAAAPFGGVKASGLGREGGRQGLEEFVETKYLCIDL 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: 554 Number of extensions: 29 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: 487 Length adjustment: 34 Effective length of query: 463 Effective length of database: 453 Effective search space: 209739 Effective search space used: 209739 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