Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_008807572.1 KVAR_RS22260 5-carboxymethyl-2-hydroxymuconate semialdehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000025465.1:WP_008807572.1 Length = 488 Score = 352 bits (902), Expect = e-101 Identities = 200/481 (41%), Positives = 278/481 (57%), Gaps = 15/481 (3%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 +ING+ + + F +P G LA+VAS A+ N+AV A+ F W+ L P K Sbjct: 7 WINGK--NVAGADYFHTTNPATGEVLAEVASGGEAEINQAVAAAKEAFPK--WANL-PMK 61 Query: 83 RKAKLIR-FADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDE 141 +A+L+R DL+ +NV E+A +ET D G PI + ++ IP A+ + AE ++ + Sbjct: 62 ERARLMRRLGDLIDQNVPEIAAMETADTGLPIHQTKNVLIPRASHNFEFFAEVCQQMNGK 121 Query: 142 VAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAI 201 P L +PVGV + PWN P + A WK+ P LA GN+ VLK SE SPLTA Sbjct: 122 TYPVDDKMLNYTLVQPVGVCALVSPWNVPFMTATWKVAPCLALGNTAVLKMSELSPLTAD 181 Query: 202 RIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNM 261 R+ +LA+EAGIPAGVLNV+ GYG T G AL H DV + FTG T + +M AG + Sbjct: 182 RLGELALEAGIPAGVLNVVQGYGATAGDALVRHHDVRAVSFTGGTATGRNIMKNAG---L 238 Query: 262 KRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLPM 321 K+ +E GGKSP ++F DA D++ A +AA I GE CTAGSR+ +++SI +F+ Sbjct: 239 KKYSMELGGKSPVLIFEDA-DIERALDAALFTIFSINGERCTAGSRIFIQQSIYPEFVKR 297 Query: 322 VVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEE---- 377 E + G+P DP T VGAL+ Q V YI G ++GA LLAGG + Sbjct: 298 FAERANRLRVGDPTDPNTQVGALISKQHWEKVSGYIRLGIEEGATLLAGGADKPSDLPAH 357 Query: 378 -TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTS 436 G ++ PT+ V N MR+AQEEIFGPV ++ F E + +AND YGLA+ IWT Sbjct: 358 LKAGNFLRPTVLADVDNRMRVAQEEIFGPVACLLPFKDEAEGLRLANDVEYGLASYIWTQ 417 Query: 437 DISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIK 496 D+SK + AR + AG V+VN + D+ PFGG K SG GR+ ++ E + E+K I Sbjct: 418 DVSKVLRLARGIEAGMVFVNTQNVRDLRQPFGGVKASGTGREGGEYSFEVFAEMKNVCIS 477 Query: 497 L 497 + Sbjct: 478 M 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: 635 Number of extensions: 32 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: 488 Length adjustment: 34 Effective length of query: 463 Effective length of database: 454 Effective search space: 210202 Effective search space used: 210202 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