Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_012541945.1 KVAR_RS14460 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000025465.1:WP_012541945.1 Length = 499 Score = 334 bits (857), Expect = 4e-96 Identities = 195/482 (40%), Positives = 280/482 (58%), Gaps = 12/482 (2%) Query: 19 ENRLFINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLS 78 ++ L+I+G AA DP T +A A D+DRA+ +A F W+ Sbjct: 19 QHGLYIDGAPCAAQSENRLTVWDPATGQAIATTADASPADVDRAVMSAWRAFVDRRWAGR 78 Query: 79 SPAKRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKV 138 +PA R+ +L + ADL+E H EELA LETL+ GK I S ++ +R+ A K+ Sbjct: 79 TPADRERILLRFADLVEQHGEELAQLETLEQGKSIAISRAFEVGCTLNWMRYTAGLTTKI 138 Query: 139 YGEVATTS------SHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKP 192 G S + A +EPVGV+A IVPWNFPL++ WK+ PALAAG S+++KP Sbjct: 139 SGRTLDVSIPFPQGARYQAWTKKEPVGVVAGIVPWNFPLMIGMWKVMPALAAGCSIVIKP 198 Query: 193 SEKSPLSAIRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQL 252 SE +PL+ +R+A LA AG+PDGV NVVTG G G AL+ H + ++FTGST TGKQ+ Sbjct: 199 SETTPLTLLRVAELATLAGIPDGVFNVVTGSGAGCGAALTAHPQVAKVSFTGSTATGKQI 258 Query: 253 LKDAGDSNMKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEE 312 + A D + RV LE GGK+ IV D D Q G F NQGQVC A +R+ +E Sbjct: 259 ARVAAD-RLTRVTLELGGKNPAIVLKDA-DPQWVIEGLMTGSFLNQGQVCAASSRIYIEA 316 Query: 313 SIADEFLALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRN 372 + D ++ +Q ++ Q G + + ++ AH D V +++ E + L+ G + Sbjct: 317 PLFDTLVSGFEQAVKSLQVGPGMQETAQINPVVSRAHCDKVAAYLEEARQQKAELISG-S 375 Query: 373 AGLAAA---IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAV 429 AG A I PT+ V+ D L+REE+FGPV+ + R E+AL+LANDS +GL A+V Sbjct: 376 AGPDAGGYYIPPTLVVNPDAGLRLTREEVFGPVVNLVRVADGEEALRLANDSDFGLTASV 435 Query: 430 WTRDLSRAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTI 489 WTRDL++A + RL+AG+V+VN++ D +PFGG KQSG GRD L+ + E K++ Sbjct: 436 WTRDLTQALNYTDRLQAGTVWVNSHTLIDANLPFGGMKQSGTGRDFGPDWLDGWCETKSV 495 Query: 490 WI 491 + Sbjct: 496 CV 497 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: 596 Number of extensions: 26 Number of successful extensions: 4 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: 499 Length adjustment: 34 Effective length of query: 461 Effective length of database: 465 Effective search space: 214365 Effective search space used: 214365 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 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