Align Aldehyde dehydrogenase 5, mitochondrial; EC 1.2.1.5 (characterized)
to candidate Echvi_1300 Echvi_1300 delta-1-pyrroline-5-carboxylate dehydrogenase, group 1
Query= SwissProt::P40047 (520 letters) >lcl|FitnessBrowser__Cola:Echvi_1300 Echvi_1300 delta-1-pyrroline-5-carboxylate dehydrogenase, group 1 Length = 543 Score = 176 bits (446), Expect = 2e-48 Identities = 137/433 (31%), Positives = 210/433 (48%), Gaps = 19/433 (4%) Query: 83 VDEAVAAAKKAFETKWSIVEPEVRAKALFNLADLVE-KHQETLAAIESMDNGKSLFCARG 141 V++A+ AA A E W +E E RA ADL+ ++ + A + K+ F A Sbjct: 81 VEQAINAALGAKEA-WETMEWEQRAAIFLKAADLIAGPYRYKMNAATMLGQSKNAFQAEI 139 Query: 142 DVAL-VSKYLRSCGGWADKIYGNVID-TGKNHFTYSIKEPL-GVCGQIIPWNFPLLMWSW 198 D A + +LR + +IY +G + + PL G + P+NF + + Sbjct: 140 DSACEIVDFLRFNVKYMTEIYKQQPPISGDGVWNRLEQRPLEGFVFALTPFNFTAIAGNL 199 Query: 199 KIGPALATGNTVVLKPAETTPLSALFASQLCQEAGIPAGVVNILPGSGRVVGERLSAHPD 258 PA+ GNTVV KPA T +A Q+ +EAG+P GV+N++ G GE + HP+ Sbjct: 200 PTAPAMM-GNTVVWKPAYTQIYTANLLMQVFREAGVPDGVINLVYVDGPAAGEVIFEHPE 258 Query: 259 VKKIAFTGSTATGRHIMKVAADTVKK------VTLELGGKSPNIVFADADLDKAVKNIAF 312 I FTGSTA + I K + ++K + E GGK I AD + + Sbjct: 259 FAGIHFTGSTAVFQTIWKTIGNNIEKYKSYPRIVGETGGKDFVIAHKSADAKQLATGLVR 318 Query: 313 GIFYNSGEVCCAGSRIYIQDTVYEEVLQKLKDYTESLKVGDPFDEEVFQGAQTSDKQLHK 372 G F G+ C A SR YI ++E+V + +++ S+K+G P D F A +K K Sbjct: 319 GAFEFQGQKCSAASRAYIPSNLWEDVKKYMQEDLASIKMGGPEDFSNFINAVIDEKSFDK 378 Query: 373 ILDYVDVAKSEGARLVTGGARHGSKGYFVKPTVFADVKEDMRIVKEEVFGPIVTVSKFST 432 I Y+D AKS+G +V GG SKGYFV+PTV + EE+FGP++T+ + Sbjct: 379 IAKYIDTAKSDGLEVVAGGHYDKSKGYFVEPTVLLTKDPMYTTMCEEIFGPVLTIYVYQE 438 Query: 433 --VDEVIAMAND-SQYGLAAGIHTNDINKAVDVSKRVK--AGTVWIN--TYNNFHQNVPF 485 +E + + + S YGL I ++D A +++++ AG +IN PF Sbjct: 439 DHFEEALELVDQTSPYGLTGAIFSHDRYAAQLATQKLRNAAGNFYINDKPTGAVVGQQPF 498 Query: 486 GGFGQSGIGREMG 498 GG +SG + G Sbjct: 499 GGARKSGTNDKAG 511 Lambda K H 0.317 0.134 0.390 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: 667 Number of extensions: 35 Number of successful extensions: 2 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: 520 Length of database: 543 Length adjustment: 35 Effective length of query: 485 Effective length of database: 508 Effective search space: 246380 Effective search space used: 246380 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