Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_110804272.1 C8J30_RS01350 aldehyde dehydrogenase family protein
Query= reanno::pseudo5_N2C3_1:AO356_12580 (497 letters) >NCBI__GCF_003217355.1:WP_110804272.1 Length = 504 Score = 326 bits (836), Expect = 1e-93 Identities = 185/478 (38%), Positives = 275/478 (57%), Gaps = 14/478 (2%) Query: 23 FINGEYTDAVSGETFDCLSPVDGRLLGKIASCDVADAQRAVENARATFNSGVWSRLAPSK 82 FI G++T V G+ FD ++P+ G + ++A AD + A++ A A G W + + Sbjct: 20 FIGGKWTPPVGGQYFDNITPITGEKICEVARSTAADVELALDAAHAA--KGEWGTTSAAH 77 Query: 83 RKTTMIRFAGLLKQHAEELALLETLDMGKPISDSLNIDVPGAAQALSWSGEAIDKLYDEV 142 R +++ A L+Q+ + LA ET D GKPI ++ D+P + + + + Sbjct: 78 RSNVLLKIADRLEQNLDLLAAAETWDNGKPIRETTAADIPLSVDHFRYFAGVLRGQEGSM 137 Query: 143 AATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGPALSTGNSVVLKPSEKSPLTAIR 202 + +D + EP+GVVG I+PWNF ++MA WKL PAL+ GN +VLKP+E++P +AI Sbjct: 138 SEIDNDTVAYHYHEPLGVVGQIIPWNFSILMAAWKLAPALAAGNCIVLKPAEQTP-SAIM 196 Query: 203 IAALAIEAGIPKGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMIYSGESNMK 262 + I+ +P GVLN++ G G VG LA + + FTGST+ +++M Y+ E N+ Sbjct: 197 VLMDVIKDLLPPGVLNIVNGMGPDVGAPLARSNRIAKIAFTGSTETGRKIMQYATE-NLI 255 Query: 263 RIWLEAGGKSPNIVFAD--APD---LQAAAESAASAIAFNQGEVCTAGSRLLVERSIKDT 317 + LE GGKSPNI F+D A D L A E AFNQGEVCT SR L++ I + Sbjct: 256 PVTLELGGKSPNIFFSDVMAKDDAFLDKAVEGFV-LFAFNQGEVCTCPSRALIQEDIYEE 314 Query: 318 FLPLVIEALKGWKPGNPLDPATNVGALVDTQQMNTVLSYIEAGHSDGAKLVAGGKRIL-- 375 F+ I +K K G+P T VGA +Q + +LSY++ G +GA+++ GG Sbjct: 315 FIARAIARVKAIKQGDPRLMETMVGAQASQEQQDKILSYLKIGREEGAQVLTGGDAASLG 374 Query: 376 -EETGGTYVEPTIFDGVSNAMKIAQEEIFGPVLSVIAFDTAEQAIEIANDTPYGLAAAVW 434 + G Y++PTI G N M++ QEEIFGPV+SV F ++A+ IANDT YGL A VW Sbjct: 375 GDLANGFYIQPTILKG-HNKMRVFQEEIFGPVVSVTTFKDEDEALHIANDTMYGLGAGVW 433 Query: 435 TKDISKAHLTAKALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHAFDKYTELKS 492 ++DI+ + + ++AG VWVN Y A FGG+KQSG GR+ D Y + K+ Sbjct: 434 SRDINTCYRFGRHIQAGRVWVNNYHAYPAHAAFGGYKQSGIGRETHKMMLDHYQQTKN 491 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: 616 Number of extensions: 33 Number of successful extensions: 6 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: 504 Length adjustment: 34 Effective length of query: 463 Effective length of database: 470 Effective search space: 217610 Effective search space used: 217610 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