Align Peroxisomal bifunctional enzyme; PBE; PBFE; EC 4.2.1.17; EC 5.3.3.8; EC 1.1.1.35 (characterized)
to candidate SM_b21632 SM_b21632 3-hydroxyacyl-CoA dehydrogenase
Query= SwissProt::Q08426 (723 letters) >FitnessBrowser__Smeli:SM_b21632 Length = 438 Score = 245 bits (626), Expect = 3e-69 Identities = 156/441 (35%), Positives = 227/441 (51%), Gaps = 26/441 (5%) Query: 268 LQYAFFAERKANKWSTPSGASWKTASARPVSSVGVVGLGTMGRGIVISFARARIPVIAVD 327 L+Y F AER A +G RP+ S V+G GTMG GI + A +P++ V+ Sbjct: 20 LRYVFHAERAARHPPALAGIE-----PRPIRSAAVIGGGTMGTGIAAALLHAGLPLVLVE 74 Query: 328 SDKNQLATANKMITSVLEKEASKMQQSGHPWSGPKPRLTSSVK--ELGGVDLVIEAVFEE 385 D+ + A + ++ + + + S + +T S + DL+IEAVFE+ Sbjct: 75 RDEAAVERALARLRTIFDGAVKRGRISAGLAAERLAGVTGSTDYTAIAEADLIIEAVFED 134 Query: 386 MSLKKQVFAELSAVCKPEAFLCTNTSALDVDEIASSTDRPHLVIGTHFFSPAHVMKLLEV 445 + +K+ VF L+AVC+ +A L TNTS LD + IA+ +G HFFSPA VMKLLE+ Sbjct: 135 LDVKRDVFRRLAAVCRADAILATNTSYLDPERIAADIGSRERFLGLHFFSPAQVMKLLEI 194 Query: 446 IPSQYSSPTTIATVMNLSKKIKKIGVVVGNCFGFVGNRMLNPYYNQAYFLLEEGSKPEEV 505 +P+Q ++P +AT L++ + KI V G GF+GNR+L QA LL G+ P V Sbjct: 195 VPTQATAPDVLATGFALARMLNKIPVRAGISDGFIGNRILKVTRAQAERLLLSGATPAAV 254 Query: 506 DQVLEEFGFKMGPFRVSDLAGLDVGWKSRKGQGLTGPTLLPGTPARKRGNRRYCPIPDVL 565 D + FG MGPF DL GLD+ R+ AR RG + P+ D L Sbjct: 255 DAAMRAFGLPMGPFEAQDLGGLDIAAFQRRA-------------ARARGETTFAPVADRL 301 Query: 566 CELGRFGQKTGKGWYQYDKPLGRIHKPDPWLSKFLSRYRKTHHIEPRTISQDEILERCLY 625 + RFGQK+G GWY Y P R +P +++ ++ + R + I+ L+ Sbjct: 302 SAIERFGQKSGGGWYDY-APGDRTPRPSATVARIIA--EEARGWPRRDWDEASIVGCILW 358 Query: 626 SLINEAFRILGEGIAASPEHIDVVYLHGYGWPRHKGGPMFYASTVGLPTVLEKLQKYYRQ 685 ++NEA RIL +G A ID+V +HGYG+PR +GG M +A GL V L Sbjct: 359 PMVNEAARILEDGTALRASDIDLVEIHGYGFPRWRGGLMHHAEAHGLHKVAGALSGLAEA 418 Query: 686 NPDIPQLEPSDYLKKLASQGN 706 P P D L + AS+G+ Sbjct: 419 GLADP---PCDPLLRAASRGS 436 Lambda K H 0.319 0.136 0.405 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: 654 Number of extensions: 31 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: 723 Length of database: 438 Length adjustment: 36 Effective length of query: 687 Effective length of database: 402 Effective search space: 276174 Effective search space used: 276174 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 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