Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_052717556.1 VL52_RS20940 NADP-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000971335.1:WP_052717556.1 Length = 486 Score = 296 bits (757), Expect = 1e-84 Identities = 171/472 (36%), Positives = 264/472 (55%), Gaps = 8/472 (1%) Query: 21 RAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAP 80 + ++ G++ DA +G++ +P G + +V A+A RAV A F + W + Sbjct: 13 QCYLGGQWLDADNGQSIAVQNPATGETVGQVPKMGAAEAERAVAAAARAFPA--WKAKSA 70 Query: 81 AKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYD 140 +R A L R+ DL+ + ++LA++ T + GKP+ ++ +I A I W AE +VY Sbjct: 71 KERAAILRRWFDLIIAHQQDLAVILTSEQGKPLAEAKG-EIAYGASYIEWYAEEAKRVYG 129 Query: 141 EVAPTPH-DQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLT 199 ++ P P D+ LVT+EP+GV AI PWNFP M K PALA G ++V++P+ ++PL+ Sbjct: 130 DIVPGPAGDRRVLVTKEPIGVTAAITPWNFPSAMITRKAAPALAAGCTMVVRPASQTPLS 189 Query: 200 AIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGES 259 A+ +A+LA AGIP GV +V+ G +G L V FTGST++ ++L+ Sbjct: 190 ALALAELAERAGIPPGVFSVITGGSSEIGAVLTGSDAVKKFSFTGSTEVGRKLIAQCA-G 248 Query: 260 NMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFL 319 +K++ +E GG +P IVF DA DL AA E A + N G+ C +R+ V+ + D F Sbjct: 249 TVKKVSMELGGNAPFIVFDDA-DLDAAVEGALISKYRNAGQTCVCANRIYVQDGVYDAFA 307 Query: 320 PMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETG 379 A+ K GN L+ + G L+D + V +I G +L+AGGKR G Sbjct: 308 DKFAAAVATLKVGNGLEAGVSQGPLIDQNAVAKVEEHIADALAKGGRLIAGGKR--HALG 365 Query: 380 GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDIS 439 ++ EPT+ VT M++A+EE FGP+ + F T EEA+ +ANDT +GLA+ + D+ Sbjct: 366 HSFFEPTLIADVTRDMKVAREETFGPLAPLFRFKTEEEAIRLANDTEFGLASYFYARDVG 425 Query: 440 KAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 + + A + G V VN + APFGG KQSG GR+ S + +E Y E+K Sbjct: 426 RIFRVAEGLEYGMVAVNSGLLSNEAAPFGGVKQSGLGREGSKYGIEDYLEIK 477 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: 567 Number of extensions: 31 Number of successful extensions: 5 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: 486 Length adjustment: 34 Effective length of query: 463 Effective length of database: 452 Effective search space: 209276 Effective search space used: 209276 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