GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Escherichia coli BW25113

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate 14185 b0039 crotonobetaine reductase subunit II, FAD-binding (NCBI)

Query= reanno::pseudo6_N2E2:Pf6N2E2_2191
         (387 letters)



>FitnessBrowser__Keio:14185
          Length = 380

 Score =  172 bits (435), Expect = 2e-47
 Identities = 108/354 (30%), Positives = 171/354 (48%), Gaps = 3/354 (0%)

Query: 34  AQIDIDNLFPADMWRKFGDMGLLGITVPEEYGGAGLGYLAHVVAMEEISRGSASVALSYG 93
           A+ D D+++P    +   DMG+  + +PEE+GG   G++       E+ R  A   + Y 
Sbjct: 30  AECDRDSVYPERFVKALADMGIDSLLIPEEHGGLDAGFVTLAAVWMELGRLGAPTYVLYQ 89

Query: 94  AHSNLCVNQINRNGNHEQKTKYLPKLISGEHIGALAMSEPNAGSDVVSMKLRADKRGDKY 153
                  N   R G  EQ  K +    +G+ +   A++EP AGSDV S+K    +R  K 
Sbjct: 90  LPGGF--NTFLREGTQEQIDKIMAFRGTGKQMWNSAITEPGAGSDVGSLKTTYTRRNGKI 147

Query: 154 VLNGSKTWITNGPDANTYVIYAKTDLEKGPHGITAFIVERDWKGFSRSNKFDKLGMRGSN 213
            LNGSK +IT+       V+ A+          T + V+    G  +  K +KLG+R  +
Sbjct: 148 YLNGSKCFITSSAYTPYIVVMARDGASPDKPVYTEWFVDMSKPGI-KVTKLEKLGLRMDS 206

Query: 214 TCELFFDDVEVPEDNILGALNGGVKVLMSGLDYERVVLSGGPTGIMQACMDLIVPYIHDR 273
            CE+ FDDVE+ E ++ G    G   +    D+ER +++    G      +    Y + R
Sbjct: 207 CCEITFDDVELDEKDMFGREGNGFNRVKEEFDHERFLVALTNYGTAMCAFEDAARYANQR 266

Query: 274 KQFGQSIGEFQLIQGKVADMYTQLNASRAYLYAVAQACERGETTRKDAAGVILYSAERAT 333
            QFG++IG FQLIQ K A M  +LN+ +  LY  A   + G  T  DAA    + A  A 
Sbjct: 267 VQFGEAIGRFQLIQEKFAHMAIKLNSMKNMLYEAAWKADNGTITSGDAAMCKYFCANAAF 326

Query: 334 QMALDAIQILGGNGYINEFPAGRLLRDAKLYEIGAGTSEIRRMLIGRELFNETR 387
           ++   A+Q+LGG G        R  RD ++  +  G+ E++ + +GR +  + R
Sbjct: 327 EVVDSAMQVLGGVGIAGNHRISRFWRDLRVDRVSGGSDEMQILTLGRAVLKQYR 380


Lambda     K      H
   0.318    0.137    0.398 

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: 16
Number of successful extensions: 3
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: 380
Length adjustment: 30
Effective length of query: 357
Effective length of database: 350
Effective search space:   124950
Effective search space used:   124950
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: 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