Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_110207793.1 DNK54_RS15005 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_003194585.1:WP_110207793.1 Length = 501 Score = 369 bits (947), Expect = e-106 Identities = 213/479 (44%), Positives = 287/479 (59%), Gaps = 19/479 (3%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FING +TD +G+ E SP G +A VA A+ + AV A+A +GVW PA+ Sbjct: 9 FINGAWTD--NGQVLEVRSPATGELVATVAKGGAAEIDAAVAAAKAAHAAGVWRNTPPAE 66 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPG--------AAQAIHWTAEA 134 R A + A L +EELA L++ + G I + ++ + AAQA + E Sbjct: 67 RAALINAVAGDLAGRLEELAALQSRENGATIRVTGALHVGLSIANMQFIAAQAAEYEFE- 125 Query: 135 IDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSE 194 K E+ P P + G++ REP+GVVGAIVPWN PLL WK+ PALA GN+VVLKP E Sbjct: 126 --KAGPEIGPVPAE--GILRREPLGVVGAIVPWNIPLLTIVWKVTPALAAGNTVVLKPDE 181 Query: 195 KSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMV 254 +PL A+ +A+ AG+PAGVLNV+ G GH G L+ H DV + FTGST++ K ++ Sbjct: 182 HAPLLALELAKAFEAAGLPAGVLNVVVGEGHDAGARLSQHPDVRKIGFTGSTEVGKSIL- 240 Query: 255 YAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSI 314 A NMKR+ LE GGK PNI+ DA DL A + A A N GE C AG+RLLV S Sbjct: 241 GASADNMKRVTLELGGKGPNILLDDA-DLDVAIDGAIYACMANNGEACEAGTRLLVPNSR 299 Query: 315 KDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRT 374 KD+ + +V + K GNPLDP T +G L+ Q + VL++I GAK+ GG Sbjct: 300 KDEIVERLVARVGTMKIGNPLDPATDIGPLITADQRDRVLAHIAKAETQGAKVAIGGSAP 359 Query: 375 LEE--TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAG 432 E G +VEPT+ VT +M +A EE+FGPVLSV+ +DT +EA+AIANDT YGL+AG Sbjct: 360 AGEEFANGYFVEPTVLTDVTPSMTVACEEVFGPVLSVLGYDTVDEAIAIANDTEYGLSAG 419 Query: 433 IWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 +W +D ++ AR + AG ++VN + PFGG+KQSG GR+ +AL+ YTE K Sbjct: 420 VWGTDETRVLDVARQLEAGMIYVNDWHVLHPAYPFGGYKQSGLGREGGPNALDAYTEQK 478 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: 698 Number of extensions: 43 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: 501 Length adjustment: 34 Effective length of query: 463 Effective length of database: 467 Effective search space: 216221 Effective search space used: 216221 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