Align Peroxisomal multifunctional enzyme A; MFE-A; MFE-1; EC 1.1.1.35 (characterized)
to candidate WP_043917837.1 jaqu_RS04975 3-oxoacyl-ACP reductase FabG
Query= SwissProt::Q9NKW1 (441 letters) >NCBI__GCF_000877395.1:WP_043917837.1 Length = 245 Score = 116 bits (291), Expect = 7e-31 Identities = 79/244 (32%), Positives = 117/244 (47%), Gaps = 20/244 (8%) Query: 8 KVVIVTGAGGGIGKVYALEFAKRGAKVVVNDLGGSHTGQGSSSKAADKVVEEIKAAGGTA 67 K +VTGA GGIG A RGA V ++ G+ + + EE+ Sbjct: 7 KAALVTGASGGIGAAIARTLHGRGATVGLS---------GTREEPLKALAEELGERANVL 57 Query: 68 VANYDSVEDGEKIVQTAMDSFGGVDILINNAGILRDVSFGKMTDGDWDLVYRVHAKGAYK 127 N + + + A ++ G VDIL+NNAG+ RD F +M++ +W V V+ A++ Sbjct: 58 PCNLSDADAVNALPKQAAEAMGAVDILVNNAGVTRDNLFMRMSEEEWAQVIEVNLTAAFR 117 Query: 128 LSRAAWNHMREKNFGRIIMTSSAAGLYGNFGQANYGSMKMALVGLSNTLAQEGKSKNIHC 187 LS+ M + +GRI+ SS G GN GQ NY + K LVG+S +LA E S+ I Sbjct: 118 LSKGVLRGMMKARWGRIVNVSSVVGATGNPGQGNYAASKAGLVGMSKSLAYEVASRGITV 177 Query: 188 NTIAP-IAASRLTESV---MPPEILEQM------KPDYIVPLVLYLCHQDTT-ETGGVFE 236 N IAP A+ +T+ + +I +Q+ P+ I LYL + TG V Sbjct: 178 NAIAPGFIATAMTDKLTDDQKSKIDDQIPMGRMGTPEEIAAAALYLASDEAAYVTGAVLH 237 Query: 237 VGAG 240 V G Sbjct: 238 VNGG 241 Score = 28.5 bits (62), Expect = 2e-04 Identities = 27/126 (21%), Positives = 54/126 (42%), Gaps = 9/126 (7%) Query: 299 DGESVLVRPPKVAVPKALAATPSGSVVVDGYNASKIFTTIQGNIGAKGAELVKKINGIYL 358 +G++ LV + A+A T G G + ++ + + A EL ++ N + Sbjct: 5 NGKAALVTGASGGIGAAIARTLHGRGATVGLSGTR-----EEPLKALAEELGERAN-VLP 58 Query: 359 INIKKGTNTQAWALDLKNGSGSI---VVGAGSTKPNVTITVSDEDFVDIMTGKLNAQSAF 415 N+ A G++ V AG T+ N+ + +S+E++ ++ L A Sbjct: 59 CNLSDADAVNALPKQAAEAMGAVDILVNNAGVTRDNLFMRMSEEEWAQVIEVNLTAAFRL 118 Query: 416 TKGKLK 421 +KG L+ Sbjct: 119 SKGVLR 124 Lambda K H 0.313 0.131 0.371 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: 254 Number of extensions: 10 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 441 Length of database: 245 Length adjustment: 28 Effective length of query: 413 Effective length of database: 217 Effective search space: 89621 Effective search space used: 89621 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 bits) S2: 48 (23.1 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