Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_034271366.1 AMYHA_RS13060 5-carboxymethyl-2-hydroxymuconate semialdehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000504245.1:WP_034271366.1 Length = 500 Score = 352 bits (904), Expect = e-101 Identities = 188/474 (39%), Positives = 288/474 (60%), Gaps = 6/474 (1%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 +I+GE+ + +TF+ +DPV+ P A A G + DIDRA++AAR F G W + Sbjct: 14 YIDGEHVDSISGDTFDVLDPVSNKPYATAAAGHAADIDRAVAAAREAFTDGAWPRMKARE 73 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R VL ++AD +EA + LA LE+ DTG PI + + AA R++A+ I + + Sbjct: 74 RARVLYRVADAVEAAEDRLAELESFDTGLPITQA-KGQARRAAENFRFFADLIVAMNEDA 132 Query: 143 ATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAIR 202 + +L ++R+PVGV I PWN P +L WKL PALAAG V+LKP+E +P SA Sbjct: 133 YSVPGTQLNYVLRKPVGVAGLITPWNTPFMLESWKLAPALAAGCPVVLKPAEFTPASASL 192 Query: 203 LAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMK 262 AG+ + AGLP GV N+V G G +AGQAL H D+ I+FTG T TG+ +++ A +++K Sbjct: 193 WAGIFEAAGLPRGVFNLVNGIGEQAGQALVEHPDVPLISFTGETTTGQTIMRSAA-AHLK 251 Query: 263 RVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLALL 322 + +E GGKS IVFAD DL A +T G+F G+ C AG+R+L++ +I +EF Sbjct: 252 ELSMELGGKSPAIVFADA-DLDAAIDSTLFGVFSLNGERCTAGSRILVQRAIYEEFCGRY 310 Query: 323 KQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDG---RNAGLAAAI 379 ++A + G P DPAT +G L+ H + V ++ G+ + +LL G + + Sbjct: 311 AERASDIVVGPPHDPATEVGALVHPEHYERVLGYVEAGKREARLLAGGGRPHHLPEGNYL 370 Query: 380 GPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLSRAHR 439 PT+F DV P+A++ ++EIFGPV +T F ++++A+ LAND +YGL VWT DL R HR Sbjct: 371 APTVFADVAPDATIFQQEIFGPVAALTPFDTDDEAIALANDVKYGLAGYVWTNDLHRGHR 430 Query: 440 MSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISL 493 ++ ++AG V++N++N D+ PFGG K SG G + +++ +T + ++L Sbjct: 431 VAGSIEAGMVWLNSHNIRDLRTPFGGVKASGVGHEGGHRSIDFYTNEHIVHVAL 484 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: 606 Number of extensions: 24 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: 500 Length adjustment: 34 Effective length of query: 461 Effective length of database: 466 Effective search space: 214826 Effective search space used: 214826 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