Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_041099671.1 SUTH_RS12545 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= reanno::WCS417:GFF5420 (497 letters) >NCBI__GCF_000828635.1:WP_041099671.1 Length = 505 Score = 202 bits (514), Expect = 2e-56 Identities = 159/484 (32%), Positives = 227/484 (46%), Gaps = 21/484 (4%) Query: 23 YINGEYTAAVSGDTFECISPVDGRLLATVASCDAADAQRAVENARATFNSGVWSRLAPAK 82 +ING A E +P +GR+ VA AD RAV ARA F W AP + Sbjct: 15 WINGHADAGAGTRVGEVFNPAEGRVARQVALATRADVDRAVAAARAAFAD--WGSAAPQR 72 Query: 83 RKSAMLRFAALLKANAEELALLETLDMGKPISDSLNIDVPGAANALSWSGEAIDKIYDEV 142 R M +F L+ + ++A L + + GK + D+L +V + ++ + + Sbjct: 73 RARVMFKFRDLVDQYSTDIAKLLSAEHGKTLPDALG-EVQRGLEVIEFACGIPQLLKGQH 131 Query: 143 AATPHDQLGLVT----REPVGVVGAIVPWNFPLMMACWKLGPALSTGNSVILKPSEKSPL 198 + H G + R P+GV I P+NFP M+ W AL+ GN+ ILKPSE+ P Sbjct: 132 S---HGIGGGIDHWNQRMPLGVTAGITPFNFPFMVPMWMAPMALACGNTFILKPSERDPS 188 Query: 199 TAIRIAALAVEAGIPKGVFNVLPGYGHTVGNALALHMDVDTLVFTGSTKIAKQLLIRSGE 258 ++ A L EAG+P G FNV+ G V +AL H V + F GST IAK + G Sbjct: 189 PSLFAAELLREAGLPAGAFNVIQGDKEAV-DALLEHPFVSAVSFVGSTPIAKYIQAH-GI 246 Query: 259 SNMKRVWLEAGGKSPNIVFADAPDLQAAAESAAGAIAFNQGEVCTAGSRLLVERSIKDKF 318 ++ KRV G K+ +V DA DL AA++ GA + GE C A S + S D Sbjct: 247 AHGKRVQALGGAKNHMVVMPDA-DLDGAADALIGAAYGSAGERCMAISVAVAVGSCADDL 305 Query: 319 LPLVIEALKGWKPGNPLDPATNVGALVDTQQMNTVLSYIEAGHADGAKLVAGGKRTL--E 376 + V+ K K G +G LV + V YI AG +GAKLV G+ L E Sbjct: 306 VARVLARAKKLKVGAGDAANVEMGPLVTAVHRDKVAGYIAAGVQEGAKLVLDGREGLTGE 365 Query: 377 ETGGTYVEPTIFDGVTNAMKIAKEEIFGPVLSVITFDSAEEAVAIANDTIYGLAAAVWTA 436 G ++ PT+FD VT M I +EEIFGPVL V+ + AV + N + A +T Sbjct: 366 LAQGFFINPTLFDNVTPNMSIYQEEIFGPVLCVVRVPTFAAAVELINRHTFANGVACFTR 425 Query: 437 DISKAHLTAKALRAGSVWVNQYDGGDMT-APFGGFKQSGNG-----RDKSLHAFDKYTEL 490 D A + + G V +N M FGG+K S G ++ + + +Y + Sbjct: 426 DGGTAQAFIQKIEVGMVGINVPIPVPMAWHSFGGWKASLFGDHHIYGEEGVRFYTRYKAI 485 Query: 491 KATW 494 W Sbjct: 486 MQRW 489 Lambda K H 0.316 0.132 0.386 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: 546 Number of extensions: 26 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 497 Length of database: 505 Length adjustment: 34 Effective length of query: 463 Effective length of database: 471 Effective search space: 218073 Effective search space used: 218073 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