GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Azorhizobium caulinodans ORS 571

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_012171357.1 AZC_RS14650 isovaleryl-CoA dehydrogenase

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



>NCBI__GCF_000010525.1:WP_012171357.1
          Length = 390

 Score =  608 bits (1569), Expect = e-179
 Identities = 300/384 (78%), Positives = 330/384 (85%)

Query: 3   EAGLNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADE 62
           + G +F LGE  D LR SVR F+ +RIAP AD+ DRSN FP  LW E+G LGLLG+T +E
Sbjct: 6   QTGFDFQLGETADLLRDSVRGFSQDRIAPRADEIDRSNQFPRDLWPELGALGLLGLTVEE 65

Query: 63  AHGGAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISG 122
            +GG+GLGYL H +AMEEISRASASVGLSYGAHSNLCVNQI RNG   QK RYLPKLISG
Sbjct: 66  EYGGSGLGYLEHVIAMEEISRASASVGLSYGAHSNLCVNQIRRNGSQEQKQRYLPKLISG 125

Query: 123 EHVGALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAG 182
           EHVGALAMSEPGAGSDVVSM+ +A+K+GDRY+LNGSKMWITNGP A+ LVVYAKTDPAAG
Sbjct: 126 EHVGALAMSEPGAGSDVVSMRTRAEKKGDRYILNGSKMWITNGPIAETLVVYAKTDPAAG 185

Query: 183 PRGITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMS 242
            RGITAFL+EK F GFS  QKLDKLGMRGS+T EL+F DCEVPEENVLG VG GV VLMS
Sbjct: 186 ARGITAFLIEKGFKGFSTAQKLDKLGMRGSDTGELVFEDCEVPEENVLGQVGRGVNVLMS 245

Query: 243 GLDYERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARA 302
           GLDYER VL+ GP+GIM AC+DVV+PY+HERKQFGQPIG FQLMQGK+ADMYV MN+ +A
Sbjct: 246 GLDYERAVLAGGPIGIMQACMDVVIPYVHERKQFGQPIGTFQLMQGKIADMYVAMNSVKA 305

Query: 303 YVYAVAAACDRGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAK 362
           YVYAVA ACDRG T R+DAAG IL AAEKAT MALEAIQ LGGNGY NDYP GRLLRDAK
Sbjct: 306 YVYAVAKACDRGLTTREDAAGAILIAAEKATWMALEAIQTLGGNGYINDYPTGRLLRDAK 365

Query: 363 LYEIGAGTSEIRRMLIGRELFAET 386
           LYEIGAGTSEIRRMLIGRELF +T
Sbjct: 366 LYEIGAGTSEIRRMLIGRELFEKT 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: 481
Number of extensions: 14
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 Apr 09 2024. 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