Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_011811226.1 VEIS_RS17035 aldehyde dehydrogenase family protein
Query= reanno::pseudo13_GW456_L13:PfGW456L13_805 (497 letters) >NCBI__GCF_000015565.1:WP_011811226.1 Length = 506 Score = 344 bits (882), Expect = 5e-99 Identities = 191/476 (40%), Positives = 278/476 (58%), Gaps = 12/476 (2%) Query: 23 YINGEYTDAVSGETFECISPVDGRLLGKIASCDAADAQRAVENARATFNSGVWSRLAPTK 82 YI G + V + FE I+PV G+ I AAD +RA++ A + W + +PT+ Sbjct: 22 YIGGAWVAPVENQYFENITPVTGKPFCDIPRSTAADVERALDAAHKAKTA--WGKTSPTE 79 Query: 83 RKSTMIRFAGLLKQHAEELALLETLDMGKPISDSLYIDVPGAAQALSWSGEAIDKIYDEV 142 R + + + A ++Q+ LA ET D GKPI ++ D+P A L + I + Sbjct: 80 RATILNKMADRIEQNLPMLAAAETWDNGKPIRETTLADIPLAVDHLRYFASCIRAQEGSI 139 Query: 143 AATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGPALSTGNSVILKPSEKSPLTAIR 202 + +D EP+GVVG I+PWNFP++MA WKL PAL+ GN V++KP+E++P++ + Sbjct: 140 SQIDNDTYAYHLHEPIGVVGQIIPWNFPILMAIWKLAPALAAGNCVVMKPAEQTPVSILV 199 Query: 203 IAELAVEAGIPKGVLNVLPGYGHTVGKALALHNDVDTLVFTGSTKIAKQLLIYSGESNMK 262 + EL + +P GV+N++ G+G GK LA N + + FTG T + + Y+ + N+ Sbjct: 200 LMELVGDL-LPPGVVNIVNGFGLEAGKPLASSNRIGKIAFTGETTTGRLISQYASQ-NLI 257 Query: 263 RVWLEAGGKSPNIVFADAPNLQDA----AEAAAGAIAFNQGEVCTAGSRLLVERSIKDKF 318 V LE GGKSPNI FAD + DA A A NQGEVCT SR+LV+ SI D+F Sbjct: 258 PVTLELGGKSPNIFFADVMDKDDAFFDKALEGFAMFALNQGEVCTCPSRVLVQESIYDRF 317 Query: 319 LPLVIEALKAWKPGNPLDPATNVGALVDTQQMNTVLSYIESGHADGARLVAGGKRTLQE- 377 + I + A G+PLD AT +GA ++Q+ +LSY + G +GAR++ GG+R L + Sbjct: 318 IERAIGRVAAITQGSPLDMATMIGAQASSEQLEKILSYFDIGKQEGARVLIGGERNLLKG 377 Query: 378 --TGGTYVEPTIFDGVSNAMKIAQEEIFGPVLSVIEFDSAEEAIAIANDTPYGLAAAVWT 435 GG Y++PT+F G N M+I QEEIFGPV+SV F + E+A+ IANDT YGL A VW+ Sbjct: 378 DLEGGYYIKPTVFKG-HNKMRIFQEEIFGPVVSVTTFKNEEDALEIANDTLYGLGAGVWS 436 Query: 436 ADISKAHLTARALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHAFDKYTELK 491 D++ A + ++AG VW N Y A FGG+K SG GR+ + Y + K Sbjct: 437 RDMNTAFRMGKGIQAGRVWTNCYHLYPAHAAFGGYKNSGIGRENHKMMLNHYQQTK 492 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: 663 Number of extensions: 28 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: 506 Length adjustment: 34 Effective length of query: 463 Effective length of database: 472 Effective search space: 218536 Effective search space used: 218536 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