Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate 3608023 Dshi_1430 aldehyde dehydrogenase (RefSeq)
Query= BRENDA::P23883 (495 letters) >FitnessBrowser__Dino:3608023 Length = 487 Score = 312 bits (800), Expect = 1e-89 Identities = 190/463 (41%), Positives = 261/463 (56%), Gaps = 20/463 (4%) Query: 38 ETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAKRKAVLNKLADLMEAH 97 + +P T +A+I ++DRA++AAR FE G+WS + R +L+KL + + AH Sbjct: 29 DVTNPATGEKIAQIPACGPDEVDRAVTAARRAFEDGEWSRLTAVDRGRLLHKLGEAITAH 88 Query: 98 AEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEVATTSSHELAMIVREP 157 +ELA E DTGKP+ + R D+ AAR +Y A DKV+GE S + EP Sbjct: 89 GQELAEWEAKDTGKPLAQA-RADMVAAARYFEYYGAAADKVHGETIPFLSGYQVQTIFEP 147 Query: 158 VGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAIRLAGLAKEAGLPDGVL 217 GV I+PWN+P + PALA GN+V+LKP+E + L+ +R+A LA E G P G + Sbjct: 148 YGVTGHIIPWNYPAQMFGRSCAPALAMGNAVVLKPAEDACLTPLRIAELALEVGFPGGAI 207 Query: 218 NVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMKRVWLEAGGKSANIVF 277 NVVTG+G EAG AL+ H D+D ++FTGS G +++ A N LE GGKS IVF Sbjct: 208 NVVTGYGQEAGAALTTHRDVDFLSFTGSPEVG-VMIQTAAARNHIGCTLELGGKSPQIVF 266 Query: 278 ADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLALLKQ-----QAQNWQPG 332 AD DL A GI N GQ C AG+R L++ I D LA LK A WQ Sbjct: 267 ADA-DLDAAIPVLLNGIVQNGGQTCSAGSRALIQRDIFDAVLARLKAGFEALTAAPWQEN 325 Query: 333 HPLDPATTMGTLIDCAHADSVHSFIRE-GESKGQLLLDGRNAGLAAAIG----PTIFVDV 387 L P LI V FI E G + L+ GR A A+ G P +F V Sbjct: 326 GNLGP------LISHKQKRRVEGFIAEGGGADAPLVARGRIAASASEAGSFVAPALFGPV 379 Query: 388 DPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLSRAHRMSRRLKAG 447 L+REE+FGPVL FT E A+++AN + YGL A+VW+ D R R+++RL+ G Sbjct: 380 IEGHVLAREEVFGPVLSCIPFTDEADAIRIANATDYGLVASVWSADGGRQMRLAKRLRVG 439 Query: 448 SVFVNNYN-DGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTI 489 VF+N Y G + +PFGG ++SG+GR+K AL +F+++KT+ Sbjct: 440 QVFLNCYGAGGGIELPFGGMRKSGHGREKGFAALHEFSQIKTV 482 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: 611 Number of extensions: 30 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: 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 Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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