Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_012707191.1 NGR_RS14395 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000018545.1:WP_012707191.1 Length = 492 Score = 358 bits (920), Expect = e-103 Identities = 204/478 (42%), Positives = 273/478 (57%), Gaps = 6/478 (1%) Query: 21 RAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAP 80 + I+G++ DA GETFE +P G A + DA RAVE A F SG W +L Sbjct: 5 KMLIDGQWADAALGETFETRNPYTGDVWAAIPKGTKEDAERAVEAAHKAFTSGTWPKLTA 64 Query: 81 AKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYD 140 + R L R DL+ +N E LA +E D GK I + + Q H+ DK+ Sbjct: 65 SDRGHLLRRLGDLIAENAERLARIEVTDNGKLINEML-FQLKYIPQWYHYFGGLADKIEG 123 Query: 141 EVAPTPHDQLGLVTR-EPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLT 199 V P + TR EP+GV I PWN PLL+ +KL PALA GN+ V KPSE + + Sbjct: 124 AVIPIDKPETFNYTRNEPLGVCVGITPWNSPLLLLSYKLAPALAAGNTFVAKPSEFTSAS 183 Query: 200 AIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGES 259 + A+L +AG P GV NV+ G+G VG+ L H V + FTGS +++ A Sbjct: 184 TLEFAKLVEQAGFPPGVFNVVTGFGADVGETLTTHKHVAKIAFTGSEGTGRKIGELAAR- 242 Query: 260 NMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFL 319 N K++ LE GGKSP+IVFADA ++ A S I G+ C AGSRLLVE I D+ L Sbjct: 243 NFKKVTLELGGKSPHIVFADA-EIDNAVNGVISGIFAATGQTCIAGSRLLVESKIHDQVL 301 Query: 320 PMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKR--TLEE 377 V+ K + G+PL T VG + Q+ +L YI+ +GA+ L GG R E Sbjct: 302 EKVIALAKTARMGDPLSTSTQVGPVTTPPQLEKILGYIDIAKGEGAECLLGGARPSNSEL 361 Query: 378 TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSD 437 G +VEPTIF GV N+MRIAQEE+FGPVL+VI FDT EEA+ IANDT YGLAAG WT D Sbjct: 362 GNGWFVEPTIFAGVRNSMRIAQEEVFGPVLAVIPFDTEEEAIHIANDTNYGLAAGFWTQD 421 Query: 438 ISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWI 495 + + + + A++AG+VWVN Y +P GG+K SG GR+ + +++ Y + K+ I Sbjct: 422 MRRMLRVSAAIQAGTVWVNTYRTISYMSPLGGYKHSGIGRENGMASIQNYLQTKSVMI 479 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: 639 Number of extensions: 28 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: 492 Length adjustment: 34 Effective length of query: 463 Effective length of database: 458 Effective search space: 212054 Effective search space used: 212054 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