Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_245638142.1 HTA01S_RS19005 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_001592305.1:WP_245638142.1 Length = 487 Score = 336 bits (862), Expect = 1e-96 Identities = 189/478 (39%), Positives = 278/478 (58%), Gaps = 9/478 (1%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 FING+Y A TFE + P T A ++ + D+D A++AAR +G W+ + Sbjct: 12 FINGQYQGARSGATFEKLAPATGGLCATVSTSDADDVDTAVAAARQALRQGPWATMPGQE 71 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R L++LADL+EA+A + G+P D+P + +R++A DK+ G Sbjct: 72 RGRCLSRLADLLEANAPAFVATLAEEQGRPAFDMTVMDLPMSVDTLRYFAGWADKLEGRT 131 Query: 143 ATTSSHELAMIVR----EPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPL 198 T+ ++ EPVGV A IVPWN PL++ WKL PALAAG +V++K SE +P+ Sbjct: 132 VPTAGFMGRQMLHYTRLEPVGVAALIVPWNAPLMIAVWKLAPALAAGCTVVIKTSEDAPV 191 Query: 199 SAIRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGD 258 + +L L EAG P GV+N+V G G EAG AL+ H D+ I+FTGST G+ + ++A Sbjct: 192 AVGQLGRLVAEAGFPPGVVNIVHGMGAEAGAALTAHPDVSKISFTGSTGVGRIIAREAA- 250 Query: 259 SNMKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEF 318 ++ KRV LE GGK+A I+ D +L +A A G+F NQGQ C AG+R+L+ S+ + Sbjct: 251 ASFKRVTLELGGKAAQILLQDA-NLDEAIPGVAMGLFVNQGQTCAAGSRILVHRSLLPQV 309 Query: 319 LALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRNAGLAAA 378 L A++ + G MG LI H + V + I S+G L G L A Sbjct: 310 EQALAAAAESVRLGGAQVEGAQMGALISARHRERVQACIDTAISQGARRLSGAGGELPAE 369 Query: 379 ---IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLS 435 + PT+F DV P +++EE+FGPV + F +E +A+ LANDS+YGL A+VWTRD+S Sbjct: 370 GFFMRPTVFTDVTPGMQIAQEEVFGPVGAIIPFDTEAEAIALANDSRYGLSASVWTRDVS 429 Query: 436 RAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISL 493 AHR++ +L+ G+V +N ++ D +P+GG K SG GRD S AL+ + E K I ++L Sbjct: 430 AAHRVAAQLEVGAVAINCWSPLDARLPWGGTKDSGIGRDLSRKALDAYLEEKVISLAL 487 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: 530 Number of extensions: 25 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: 487 Length adjustment: 34 Effective length of query: 461 Effective length of database: 453 Effective search space: 208833 Effective search space used: 208833 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