Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate GFF4092 HP15_4032 betaine aldehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >FitnessBrowser__Marino:GFF4092 Length = 486 Score = 337 bits (865), Expect = 4e-97 Identities = 189/483 (39%), Positives = 286/483 (59%), Gaps = 15/483 (3%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 +ING+Y +A F+ V+P ++K+ ++D A+ AAR RG W + + Sbjct: 7 YINGQYVGSASGRLFDNVNPANGKVISKVHEAGREEVDAAVKAARAAL-RGPWGKMTLEQ 65 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R A+L+K+AD + A +E E LDTGKP + DIP A + +A+ I V E Sbjct: 66 RTAILHKVADGINARFDEFLEAECLDTGKPKSLASHIDIPRGAANFKVFADMIKNVPTES 125 Query: 143 ATTSSHE----LAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPL 198 + + L VR P GVI I PWN PLLL WK+GPALA GN+V++KPSE++P Sbjct: 126 FEMPTPDGTGALNYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPSEETPT 185 Query: 199 SAIRLAGLAKEAGLPDGVLNVVTGFGHE-AGQALSRHNDIDAIAFTGSTRTGKQLLKDAG 257 + L + KEAG+PDGV NVV GFG + AG L+ H +D FTG T TG+ ++K A Sbjct: 186 TTALLGEVMKEAGVPDGVYNVVHGFGGDSAGAYLTEHPQVDGFTFTGETGTGEVIMKAAA 245 Query: 258 DSNMKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADE 317 ++ + LE GGK+A +VFADC D+++A T F N GQVC+ R+ +E SI DE Sbjct: 246 -KGIRDISLELGGKNAGLVFADC-DMEKAIEGTMRSAFANCGQVCLGTERVYVERSIFDE 303 Query: 318 FLALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRN----- 372 F+ LK+ A+ + G P D +G L+ H + V S+ ++ G ++ G Sbjct: 304 FVGRLKEAAEGLKIGPPDDADANLGPLVSLKHREKVLSYYQKAVDDGATVVTGGGVPDMP 363 Query: 373 AGLA--AAIGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVW 430 A LA A + PTI+ + ++++ +EIFGP + F +EE+A++LAN YGL +A+W Sbjct: 364 AELAGGAWVEPTIWTGLPDDSAVVTDEIFGPCCHIRPFDTEEEAIELANSLPYGLASAIW 423 Query: 431 TRDLSRAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIW 490 + +++RAHR++ +++AG ++VN++ D+ PFGG KQSG GR+ +H+LE +TE+K I Sbjct: 424 SENITRAHRVAGQIEAGIIWVNSWFLRDLRTPFGGSKQSGVGREGGVHSLEFYTEMKNIC 483 Query: 491 ISL 493 + L Sbjct: 484 VKL 486 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: 612 Number of extensions: 32 Number of successful extensions: 7 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: 486 Length adjustment: 34 Effective length of query: 461 Effective length of database: 452 Effective search space: 208372 Effective search space used: 208372 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