Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_090271786.1 BLU11_RS01865 aldehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_900105005.1:WP_090271786.1 Length = 506 Score = 339 bits (869), Expect = 2e-97 Identities = 198/484 (40%), Positives = 286/484 (59%), Gaps = 18/484 (3%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 FI GE+ A+ E F PVT +A+ R K+ DID+A+ AA + W +SP Sbjct: 22 FIGGEFMVPADGEYFTNTSPVTGEVIAEFPRSKAADIDKALDAAHAAADA--WGKTSPQD 79 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R VL K+AD +EA+ E LA+ +T D GK IR +L D+P AA R++A I G Sbjct: 80 RALVLLKIADRIEANLEMLAVADTWDNGKAIRETLNADVPLAADHFRYFAGCIRAQEGSA 139 Query: 143 ATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAIR 202 A + H +A EP+GV+ I+PWNFPLL+ WKL PALAAGN V+LKP+E++PLS Sbjct: 140 AEINEHTVAYHFHEPLGVVGQIIPWNFPLLMAAWKLAPALAAGNCVVLKPAEQTPLSMSL 199 Query: 203 LAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMK 262 A L + LP GVLN+V GFG EAG+AL+ I IAFTGST G ++ A + N+ Sbjct: 200 FAELVGDL-LPPGVLNIVQGFGKEAGEALATSTRIAKIAFTGSTPVGAHIMHCAAE-NII 257 Query: 263 RVWLEAGGKSANIVFADCPD-----LQQAASATAAGIFYNQGQVCIAGTRLLLEESIADE 317 +E GGKS NI F D +++AA G F+NQG+VC +R L++ESI + Sbjct: 258 PSTVELGGKSPNIFFEDIMSAEPEFIEKAAEGLVLG-FFNQGEVCTCPSRALVQESIFEP 316 Query: 318 FLALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRNA---- 373 F+ + ++ + + G PLD T +G + + S++ + +G +L G A Sbjct: 317 FMNEVMKKIKKIKRGDPLDTETMVGAQASEQQFEKILSYLDIAQEEGAQVLTGGEAEKLE 376 Query: 374 -GLAAA--IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVW 430 GLA+ I PT+ + D + + +EEIFGPV+ VT F E +AL++AND+++GLGA +W Sbjct: 377 GGLASGYYIQPTL-LKGDNSMRVFQEEIFGPVIGVTTFKDEAEALEVANDTEFGLGAGLW 435 Query: 431 TRDLSRAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIW 490 TRD++RA+RM R +KAG V+ N Y+ FGGYK+SG GR+ L+ + + K + Sbjct: 436 TRDMNRAYRMGRGIKAGRVWTNCYHLYPAHAAFGGYKKSGVGRENHKMMLDHYQQTKNLL 495 Query: 491 ISLE 494 +S + Sbjct: 496 VSYD 499 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: 546 Number of extensions: 25 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: 506 Length adjustment: 34 Effective length of query: 461 Effective length of database: 472 Effective search space: 217592 Effective search space used: 217592 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