Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_012276124.1 SHAL_RS05100 NADP-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000019185.1:WP_012276124.1 Length = 482 Score = 280 bits (717), Expect = 6e-80 Identities = 169/472 (35%), Positives = 256/472 (54%), Gaps = 8/472 (1%) Query: 21 RAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAP 80 + +I+G++ +A++GE E P + + V + A+ A + W L Sbjct: 12 QCYIDGQWLEAINGEKVEIADPATHKVIGSVPVMGTTETKAAITAAEKALPA--WRALTA 69 Query: 81 AKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYD 140 +R AKL R+ +LL ++ ++LAL+ T + GKP+ ++ ++ AA I W AE +VY Sbjct: 70 KERGAKLHRWFELLLEHQDDLALMMTTEQGKPLAEAKG-EVAYAASFIEWFAEEAKRVYG 128 Query: 141 EVAPTPH-DQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLT 199 + P D+ +V ++ VGV AI PWNFP M K PALA G ++V+KP+ ++P T Sbjct: 129 DTIPGHQGDKRLMVIKQSVGVTAAITPWNFPAAMITRKAAPALAAGCTMVVKPAPQTPFT 188 Query: 200 AIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGES 259 A+ +A+LA AGIPAGV +V+ G +G L + V L FTGST + +LM + Sbjct: 189 ALALAELAERAGIPAGVFSVVTGDAIAIGNELCSNPVVRKLSFTGSTPVGIKLMQQCAPT 248 Query: 260 NMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFL 319 +K++ LE GG +P IVF DA D+ AA E A A N G+ C +R+ V+ + D+F Sbjct: 249 -LKKMSLELGGNAPFIVFNDA-DIDAAVEGAMIAKYRNAGQTCVCANRIYVQDRVYDEFA 306 Query: 320 PMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETG 379 + A+ K G + T G L+++ + V +++ GA L AGGK L G Sbjct: 307 EKLAAAVAKLKVGVGTEAGVTTGPLINSDAVAKVQRHLDDALSKGATLFAGGK--LASLG 364 Query: 380 GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDIS 439 G + EPTI V +M +A+EE FGP+ + F ++ + ANDT +GLAA + DIS Sbjct: 365 GNFFEPTILTNVDKSMLVAKEETFGPLAPLFKFSDVDDVIEQANDTEFGLAAYFYGRDIS 424 Query: 440 KAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 K + A+ G V VN APFGG K SG GR+ S +E+Y E+K Sbjct: 425 LVWKVSEALEYGMVGVNTGLISTEVAPFGGIKSSGLGREGSKFGIEEYLEMK 476 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: 568 Number of extensions: 39 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: 482 Length adjustment: 34 Effective length of query: 463 Effective length of database: 448 Effective search space: 207424 Effective search space used: 207424 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