Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_009762358.1 MICLODRAFT_RS03140 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000262405.1:WP_009762358.1 Length = 496 Score = 424 bits (1091), Expect = e-123 Identities = 222/475 (46%), Positives = 307/475 (64%), Gaps = 4/475 (0%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 FI+ + +AA E + P+ L +A S D++RA++AAR FE G WS +P + Sbjct: 22 FIDNKAVSAASGEVMPVISPIDGTQLTVLAASDSEDMNRAVAAARRSFETGCWSGMAPRE 81 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 RK ++ K ADL++ HA E+A+L D G IR +L+ + AA IR+YAEAIDK GE+ Sbjct: 82 RKRIMLKWADLIDRHALEIAVLGVRDNGTDIRMALKGEPQSAADTIRFYAEAIDKRNGEI 141 Query: 143 ATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAIR 202 T L++I RE VGV+ I+PWNFPL++ WKL PALAAGNSV++KPSE++ LS +R Sbjct: 142 TPTRHDILSLIHREAVGVVGVIIPWNFPLMIGSWKLAPALAAGNSVVVKPSEEASLSILR 201 Query: 203 LAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMK 262 + LA EAG+P GVLN V G G G+AL H D+D + FTGS G++LL+ + SN+K Sbjct: 202 VIELAAEAGIPPGVLNAVNGRGAIVGEALGLHMDVDVLGFTGSGGVGRRLLEYSARSNLK 261 Query: 263 RVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLALL 322 RV+LE GGKS N+VFAD P+L++AA TAA IF N GQVC A +RL +E S+ +F+ + Sbjct: 262 RVYLELGGKSPNLVFADAPNLKRAARETAASIFRNNGQVCAAASRLAVERSVYKDFMEAV 321 Query: 323 KQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRNAGLAAAIG-- 380 + +A + G PL A T G L + A + I +G + G N A + G Sbjct: 322 RAEATAMRIGDPLSLAFTTGALANAAQLAKTRAAIARAAEQGATVYHGGNQLHAESGGFY 381 Query: 381 --PTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLSRAH 438 PTI DV + ++EIFGPVLV F +EE+A+ +AN++ +GL + +WTRDLS+AH Sbjct: 382 HEPTILTDVATEMDVVQQEIFGPVLVARSFDTEEEAIAIANETVFGLSSVLWTRDLSKAH 441 Query: 439 RMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISL 493 R+S R+K+G V +N Y+ D+T P GG +QSGNG D+SLHALEK+ LKT WI L Sbjct: 442 RVSNRIKSGVVHINCYSGADITAPLGGVRQSGNGSDRSLHALEKYENLKTKWIQL 496 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: 543 Number of extensions: 25 Number of successful extensions: 2 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: 496 Length adjustment: 34 Effective length of query: 461 Effective length of database: 462 Effective search space: 212982 Effective search space used: 212982 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