Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_041098592.1 SUTH_RS08615 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000828635.1:WP_041098592.1 Length = 480 Score = 309 bits (792), Expect = 1e-88 Identities = 185/475 (38%), Positives = 273/475 (57%), Gaps = 9/475 (1%) Query: 18 IEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQ 77 + INGE+ A +G T + +P G + V A+ RA++ A A F+ W Sbjct: 7 LRNACLINGEWL-AATGATLDIRNPATGEAVGSVPGFGAAETRRAIDAAHAAFHP--WRA 63 Query: 78 LAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDK 137 A+R L R+ +L+ +N E+LA L T + GKP+ ++ +I AA I W AE + Sbjct: 64 KTAAERAKILRRWFELMMENQEDLARLMTQEQGKPLAEARG-EIAYAASFIEWFAEEARR 122 Query: 138 VYDEVAPTP-HDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKS 196 +Y +V P+P D+ +V ++PVGV AI PWNFP M K+ PALA G ++V+KP+E++ Sbjct: 123 IYGDVIPSPLADRRLIVLKQPVGVCAAITPWNFPAAMITRKVAPALAAGCTMVVKPAEQT 182 Query: 197 PLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYA 256 PL+A+ +A L +AG+P GVLNV+ G +G L + V L FTGST+I + LM Sbjct: 183 PLSALALAWLGQQAGLPPGVLNVVTGEPVAIGGELTSNPKVLKLSFTGSTEIGRLLMGQC 242 Query: 257 GESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKD 316 + +K++ LE GG +P IVF DA DL AA A + N G+ C +R LV+ + D Sbjct: 243 APT-IKKMSLELGGNAPFIVFDDA-DLDAAVAGAMLSKYRNTGQTCVCTNRFLVQEGVHD 300 Query: 317 KFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLE 376 F + A+ G K G L+ T G L+D + V + GA++L GGKR + Sbjct: 301 AFAQRLAAAVAGLKVGYGLEEGVTQGPLIDGAGLAKVEELLADALAKGARVLCGGKRHAK 360 Query: 377 ETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTS 436 GGT+ EPT+ G T AMR+A+EEIFGPV + +F +A+ +ANDT +GLAA ++ Sbjct: 361 --GGTFFEPTVLAGATPAMRLAREEIFGPVAPIFSFKDEADAIRMANDTEFGLAAYFFSR 418 Query: 437 DISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 DI++A + A+ G V +N + APFGG KQSG GR+ S + +E+Y E+K Sbjct: 419 DIARAWRVGEALDYGMVGINSGMISNEVAPFGGVKQSGLGREGSKYGIEEYLEIK 473 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: 606 Number of extensions: 32 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: 480 Length adjustment: 34 Effective length of query: 463 Effective length of database: 446 Effective search space: 206498 Effective search space used: 206498 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