GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Azospirillum brasilense Sp245

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate AZOBR_RS22310 AZOBR_RS22310 isovaleryl-CoA dehydrogenase

Query= reanno::Smeli:SM_b21121
         (387 letters)



>FitnessBrowser__azobra:AZOBR_RS22310
          Length = 390

 Score =  625 bits (1611), Expect = 0.0
 Identities = 309/381 (81%), Positives = 337/381 (88%)

Query: 6   LNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHG 65
           LNF LGE  D LR +VR FA++ IAP A + DR+N FP  LWR+ G+LG+LGITA+E +G
Sbjct: 9   LNFDLGESADMLRDTVRSFAADEIAPRAAEIDRTNEFPNELWRKFGDLGVLGITAEEEYG 68

Query: 66  GAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHV 125
           GAG+GYL H VAMEEISRASASVGLSYGAHSNLCVNQI +NG   QK+RYLPKLISGEH+
Sbjct: 69  GAGMGYLEHVVAMEEISRASASVGLSYGAHSNLCVNQIRKNGTAEQKTRYLPKLISGEHI 128

Query: 126 GALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRG 185
           GALAMSEP AGSDVVSMKL+A+K+GDRYVLNG+KMWITNGPDAD LVVYAKTD  AGPRG
Sbjct: 129 GALAMSEPNAGSDVVSMKLRAEKQGDRYVLNGTKMWITNGPDADTLVVYAKTDVNAGPRG 188

Query: 186 ITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGLD 245
           ITAFL+EK+F GFS  QKLDKLGMRGSNT EL+F DCEVPEEN+LGGVG GV VLMSGLD
Sbjct: 189 ITAFLIEKSFKGFSVAQKLDKLGMRGSNTGELVFEDCEVPEENILGGVGRGVNVLMSGLD 248

Query: 246 YERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVY 305
           YER VL+ GPLGIM AC+DVVVPYLH+RKQFGQPIGEFQLMQGKLADMY  MNAA+AYVY
Sbjct: 249 YERAVLAGGPLGIMQACMDVVVPYLHDRKQFGQPIGEFQLMQGKLADMYTIMNAAKAYVY 308

Query: 306 AVAAACDRGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLYE 365
           AVA ACDRGETARKDAAG IL+AAEKAT MALEAIQ LGGNGY N+YP GRLLRDAKLYE
Sbjct: 309 AVAKACDRGETARKDAAGAILFAAEKATWMALEAIQTLGGNGYINEYPTGRLLRDAKLYE 368

Query: 366 IGAGTSEIRRMLIGRELFAET 386
           IGAGTSEIRRMLIGRELF ET
Sbjct: 369 IGAGTSEIRRMLIGRELFKET 389


Lambda     K      H
   0.318    0.135    0.391 

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: 492
Number of extensions: 10
Number of successful extensions: 1
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: 387
Length of database: 390
Length adjustment: 30
Effective length of query: 357
Effective length of database: 360
Effective search space:   128520
Effective search space used:   128520
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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