GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimC in Cupriavidus basilensis 4G11

Align pimeloyl-CoA dehydrogenase small subunit (EC 1.3.1.62) (characterized)
to candidate RR42_RS28380 RR42_RS28380 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-20677
         (380 letters)



>FitnessBrowser__Cup4G11:RR42_RS28380
          Length = 375

 Score =  301 bits (770), Expect = 3e-86
 Identities = 165/372 (44%), Positives = 216/372 (58%), Gaps = 2/372 (0%)

Query: 1   MDFDLSEEQRLLKESVEGLLKGSYDFDSRKKYAKEKGGWSRAVWGKFAEQGLLGLPFSEE 60
           MDF  ++E   L+++V     G Y    R     E        W   AE GLLGLPF  E
Sbjct: 1   MDFSYTDEHIALQDAVRRFCDGEYPAHQRGN--PEAPALCAQRWASMAELGLLGLPFDSE 58

Query: 61  DGGFGAGAVETMIVMEALGHSLVLEPYLPTVVIGGGFLRRAGSAAQKAAHLPGIIDGSKT 120
            GG G G VE M+V + LG  L    +L +VV+ G  L + G+A Q+   LP +  G   
Sbjct: 59  VGGSGQGTVELMLVAQELGRCLGGGAWLSSVVLAGQLLDQVGTARQRGRWLPEVASGKCR 118

Query: 121 FAFAQLEKNSRWDLGDVSTTAKKSGDGWVIDGEKFVVLNGEAADTLIVTARTKGGQRDRT 180
            A A  E +SR+ L  V T A+ S DGW I+G K +VL G  A+  IV ART G   D  
Sbjct: 119 LALAASESDSRYSLSRVRTRAQASADGWRIEGRKTLVLEGGDANAFIVVARTAGDVADDD 178

Query: 181 GVGVFLVPADAKGITRKGYPTQDGLHAADITFTGVQVGADAAIGDPENALELIEAVVDDA 240
           G+ +FLV A   G+   G+ T DG  AA +   GVQVG+DA +G+   AL LIEA  D A
Sbjct: 179 GLTLFLVDAKTPGVAVHGFATLDGRQAAHVVLDGVQVGSDAMLGEAGRALPLIEAATDRA 238

Query: 241 RTALCAEAVGLMDESLTTTVEYIKTRKQFGVPIGSFQVLQHRAADMFVATEQARSMAMFA 300
              LCAEA G ++  +  T E++KTRKQFG  +  FQVLQHR ADM +A EQ++SMA  A
Sbjct: 239 SAVLCAEAAGALEALIDLTAEHLKTRKQFGTTLARFQVLQHRVADMLIALEQSKSMACAA 298

Query: 301 TMAAEFDDAKERAGAIAAAKVQIGKSGKFVGQQSIQLHGGIGMTMEAKIGHYFKRLTMIE 360
            MA +  +  +R   ++AAKV +G++G+ V Q +IQLHG +GMT E ++GHY KRL +I 
Sbjct: 299 AMAVDAGEPVQRRRLVSAAKVVVGQAGRQVSQWAIQLHGAMGMTDECRVGHYAKRLLVIN 358

Query: 361 QTFGDTDHHLAR 372
           Q FGD  HHL R
Sbjct: 359 QLFGDASHHLQR 370


Lambda     K      H
   0.318    0.135    0.388 

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: 370
Number of extensions: 17
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: 380
Length of database: 375
Length adjustment: 30
Effective length of query: 350
Effective length of database: 345
Effective search space:   120750
Effective search space used:   120750
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