Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_034277076.1 AMYHA_RS13095 aldehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000504245.1:WP_034277076.1 Length = 478 Score = 373 bits (957), Expect = e-108 Identities = 212/479 (44%), Positives = 290/479 (60%), Gaps = 10/479 (2%) Query: 23 FINGE-YTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPA 81 F+ G+ + AA TF++ DP T LA + G S DID A+ AAR E W+ SPA Sbjct: 3 FLCGDTWCRAASGATFDSRDPATGEVLAVVPDGGSDDIDAAVRAARDALEDARWARISPA 62 Query: 82 KRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGE 141 +R +L ++A+L+E A+ELA LE+ D G+P+ + + GAA R++A K+ G Sbjct: 63 ERARLLWRIAELIEDRADELAELESRDQGQPLALARGVSVGGAAEHFRYFAGWCTKLDGR 122 Query: 142 VATTSSHE-LAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSA 200 V S + L R PVGV I PWNFPLL+ WKL PALA GN+V+LKP+E++PL+A Sbjct: 123 VPAHSRPDALNYTKRVPVGVCGLITPWNFPLLIAAWKLAPALACGNTVVLKPAEQTPLTA 182 Query: 201 IRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSN 260 +RLAGL EAG P GV+NVVTG G EAG+AL H+ +D ++FTGST G+ +++ A N Sbjct: 183 LRLAGLFHEAGFPPGVVNVVTG-GPEAGRALVEHDGVDKVSFTGSTEVGRSIVR-ASAGN 240 Query: 261 MKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLA 320 +KR+ LE GGK+A+++ AD D++ A + N GQVC A R + + EF Sbjct: 241 LKRLSLELGGKAASVITADS-DIEAAVAGNLRSATQNSGQVCAASARFYVARARYSEFTD 299 Query: 321 LLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRNAG-----L 375 L A+N + G LDP T MG L+ H SV S++R G +G L+ G G Sbjct: 300 RLATAAENIRLGPGLDPGTQMGPLVGEEHLSSVDSYVRSGIEQGASLVTGGARGDGPLAR 359 Query: 376 AAAIGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLS 435 + PT+F D D ++REEIFGPVL V F ++A NDSQYGL A+VWTRDL+ Sbjct: 360 GSFYQPTVFADADDEMRIAREEIFGPVLTVMPFDDIDEAATRVNDSQYGLAASVWTRDLA 419 Query: 436 RAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISLE 494 AHR++ R+ AG V VN D VP+GG K SG GR+ A+E +TE+K++WI LE Sbjct: 420 TAHRLAERINAGCVRVNMVAGIDPAVPWGGVKASGWGREMGAEAIEDYTEVKSVWIGLE 478 Lambda K H 0.317 0.133 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: 606 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: 495 Length of database: 478 Length adjustment: 34 Effective length of query: 461 Effective length of database: 444 Effective search space: 204684 Effective search space used: 204684 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 (21.7 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