Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_025761916.1 X939_RS0103685 aldehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000566685.1:WP_025761916.1 Length = 525 Score = 315 bits (807), Expect = 2e-90 Identities = 180/483 (37%), Positives = 282/483 (58%), Gaps = 16/483 (3%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 FI G++ E F+ + P+ + AR D++ A+ AA F WS ++ A Sbjct: 41 FIGGQFVPPFRGEYFDNISPIDGKVFTQAARSTKEDVELALDAAHKAFP--SWSKTAAAT 98 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R +L K+A ++E + E LA++E++D GK IR + D+P R++A I G + Sbjct: 99 RSNLLLKIAQVIEDNIEYLAVVESIDNGKAIRETRAADLPLCVDHFRYFAGVIRAEEGGI 158 Query: 143 ATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAIR 202 + + +++ + EP+GV+ I+PWNFPLL+ WK+ PALAAG V++KP+E++P S + Sbjct: 159 SEHDENTISINLHEPIGVVGQIIPWNFPLLMATWKIAPALAAGCCVVVKPAEQTPTSIMI 218 Query: 203 LAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMK 262 L L + LP+GVLN+V+GFG EAG+ L+ I ++FTG T TG+ +++ A + N+ Sbjct: 219 LMELIGDI-LPEGVLNIVSGFGVEAGKPLASSPRIAKVSFTGETTTGRLIMQYASE-NLI 276 Query: 263 RVWLEAGGKSANIVFADCPDLQQA----ASATAAGIFYNQGQVCIAGTRLLLEESIADEF 318 V +E GGKS NI F D A A A +NQG+VC +R+L+ ESI D+F Sbjct: 277 PVTMELGGKSPNIFFPSVADADDAFFDKAIEGAVLFAFNQGEVCTCPSRILVHESIYDKF 336 Query: 319 LALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRNA----- 373 ++ + ++ + + GHPLD +T MG + + S+++ G+ +G +L G A Sbjct: 337 MSRVIERTKAIKMGHPLDGSTMMGAQASNDQYEKILSYLKIGKEEGAEILAGGEAHRFEN 396 Query: 374 GLAAA--IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWT 431 G+A I PTIF + + +EEIFGPV+ VT F + E+A+++AND+ YGLGA VWT Sbjct: 397 GIAGGYYIQPTIFKGHN-KMRIFQEEIFGPVVCVTTFKTTEEAIEIANDTLYGLGAGVWT 455 Query: 432 RDLSRAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWI 491 RD +++ R ++AG V+VNNY+ PFGGYK+SG GR+ L + K + I Sbjct: 456 RDAHEIYQVPRAIQAGRVWVNNYHAYPAHAPFGGYKKSGFGRENHKMMLGYYRNTKNMLI 515 Query: 492 SLE 494 S + Sbjct: 516 SYD 518 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: 558 Number of extensions: 20 Number of successful extensions: 5 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: 525 Length adjustment: 34 Effective length of query: 461 Effective length of database: 491 Effective search space: 226351 Effective search space used: 226351 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