Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate AO353_09195 AO353_09195 aldehyde dehydrogenase
Query= reanno::pseudo6_N2E2:Pf6N2E2_4383 (497 letters) >FitnessBrowser__pseudo3_N2E3:AO353_09195 Length = 497 Score = 947 bits (2449), Expect = 0.0 Identities = 471/497 (94%), Positives = 487/497 (97%) Query: 1 MTTLTRADWEQRARDLKIEGRAFINGEYTDAVSGETFDCLSPVDGRLLGKIASCDVADAQ 60 MTTLTRADWEQRARDLKIEGRA+INGEYT AVSGETFDC+SPVDGRLLGKIASCD ADAQ Sbjct: 1 MTTLTRADWEQRARDLKIEGRAYINGEYTAAVSGETFDCISPVDGRLLGKIASCDAADAQ 60 Query: 61 RAVENARATFSSGVWSRLAPSKRKATMIRFAGLLKQHAEELALLETLDMGKPISDSLNID 120 RAVENAR+TF+SGVWSRLAP+KRKATMIRFAGLLKQHAEELALLETLDMGKPISDSL ID Sbjct: 61 RAVENARSTFNSGVWSRLAPAKRKATMIRFAGLLKQHAEELALLETLDMGKPISDSLYID 120 Query: 121 VPGAAQALSWSGEAIDKLYDEVAATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGP 180 VPGAAQALSWSGEAIDK+YDEVAATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGP Sbjct: 121 VPGAAQALSWSGEAIDKIYDEVAATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGP 180 Query: 181 ALSTGNSVVLKPSEKSPLTALRIAALAIEAGIPKGVLNVLPGYGHTVGKALALHMDVDTL 240 ALSTGNSV+LKPSEKSPLTA+R+AALA+EAGIPKGVLNVLPGYGHTVGKALALHMDVDTL Sbjct: 181 ALSTGNSVILKPSEKSPLTAIRLAALAVEAGIPKGVLNVLPGYGHTVGKALALHMDVDTL 240 Query: 241 VFTGSTKIAKQLMIYSGESNMKRIWLEAGGKSPNIVFADAPDLQAAAESAASAIAFNQGE 300 VFTGSTKIAKQLMIYSGESNMKR+WLEAGGKSPNIVFADAPDLQAAAESAASAIAFNQGE Sbjct: 241 VFTGSTKIAKQLMIYSGESNMKRVWLEAGGKSPNIVFADAPDLQAAAESAASAIAFNQGE 300 Query: 301 VCTAGSRLLVERSIKDTFLPLVIEALKGWKPGNPLDPATNVGALVDTQQMNTVLSYIEAG 360 VCTAGSRLLVERSIKD FLPLVIEALK WKPGNPLDPATNVGALVDTQQMNTVLSYIE+G Sbjct: 301 VCTAGSRLLVERSIKDKFLPLVIEALKTWKPGNPLDPATNVGALVDTQQMNTVLSYIESG 360 Query: 361 HSDGAKLVAGGKRILEETGGTYVEPTIFDGVSNAMKIAQEEIFGPVLSVIAFDTAEQAIE 420 HSDGAKLVAGGKRIL+ETGGTYVEPTIFDGVSNAMKIAQEEIFGPVLSVI FD+ E+AI Sbjct: 361 HSDGAKLVAGGKRILQETGGTYVEPTIFDGVSNAMKIAQEEIFGPVLSVITFDSVEEAIR 420 Query: 421 IANDTPYGLAAAVWTKDISKAHLTAKALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKS 480 IANDTPYGLAAAVWT DISK HLTAKALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKS Sbjct: 421 IANDTPYGLAAAVWTSDISKGHLTAKALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKS 480 Query: 481 LHAFDKYTELKSTWIKL 497 LHAFDKYTELK+TWIKL Sbjct: 481 LHAFDKYTELKATWIKL 497 Lambda K H 0.316 0.132 0.389 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: 993 Number of extensions: 33 Number of successful extensions: 1 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: 497 Length adjustment: 34 Effective length of query: 463 Effective length of database: 463 Effective search space: 214369 Effective search space used: 214369 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