Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_062735529.1 AYX06_RS09260 5-carboxymethyl-2-hydroxymuconate semialdehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_001580365.1:WP_062735529.1 Length = 523 Score = 374 bits (960), Expect = e-108 Identities = 196/474 (41%), Positives = 292/474 (61%), Gaps = 6/474 (1%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 +I+G + +A+ +TFE +DPV+ + A GK D+DRA++AAR F G WS P + Sbjct: 28 YIDGRFVDSADGDTFEVLDPVSNETYLRAAAGKKADVDRAVAAARRAFAEGPWSRMLPRE 87 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R +L+++AD++E+ LA LE+ D+G PI +L AA R++A+ I + Sbjct: 88 RSRILHRIADIVESRDARLAELESFDSGLPITQAL-GQARRAAENFRFFADLIVAQADDT 146 Query: 143 ATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAIR 202 ++ + R+P+GV I PWN P +L WKLGPALA GN+V+LKP+E +PLSA Sbjct: 147 YKVPGRQINYVNRKPIGVAGLITPWNTPFMLESWKLGPALATGNTVVLKPAEFTPLSASL 206 Query: 203 LAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMK 262 AG+ +EAGLP GV N+V G G +AG AL +H D+ I+FTG + TG+ + +A ++K Sbjct: 207 WAGIFEEAGLPQGVFNLVNGLGEDAGDALVKHPDVPLISFTGESSTGRLIFANAA-PHLK 265 Query: 263 RVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLALL 322 + +E GGKS +VFAD DL A AT G+F G+ C AG+R+L++ + DEF+ Sbjct: 266 GLSMELGGKSPAVVFADA-DLDAAVDATIFGVFSLNGERCTAGSRILVQREVYDEFVERY 324 Query: 323 KQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLL-DGRNAGLAAA--I 379 QA+ G P DP T +G L+ H D V S+I G ++G+L+ GR G + Sbjct: 325 AAQAERVVVGPPHDPRTEVGALVHPEHYDKVMSYIEIGRTEGRLVAGGGRPEGFPTGNYV 384 Query: 380 GPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLSRAHR 439 PT+F DV P A + +EEIFGPV+ +T F ++E+AL+LAN +YGL A VWT DL RAH Sbjct: 385 APTVFADVAPEARIFQEEIFGPVVAITPFDTDEEALRLANGVRYGLAAYVWTNDLRRAHN 444 Query: 440 MSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISL 493 S+ ++AG V++N+ N D+ PFGG K SG G + +++ +T+ + + I+L Sbjct: 445 FSQNIEAGMVWLNSNNVRDLRTPFGGVKASGLGHEGGYRSIDFYTDQQAVHITL 498 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: 624 Number of extensions: 29 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: 523 Length adjustment: 34 Effective length of query: 461 Effective length of database: 489 Effective search space: 225429 Effective search space used: 225429 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