GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Escherichia coli BW25113

Align D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate 18382 b4358 predicted oxidoreductase, Zn-dependent and NAD(P)-binding (RefSeq)

Query= BRENDA::S6BFC0
         (363 letters)



>FitnessBrowser__Keio:18382
          Length = 340

 Score =  159 bits (402), Expect = 1e-43
 Identities = 108/353 (30%), Positives = 172/353 (48%), Gaps = 20/353 (5%)

Query: 11  NSFVLQKQDEISFEDRPVPVAGPGQVIVNIKATGICGSDVHYWTHGRIGHFVCNGPMVLG 70
           N  + Q+  E+ ++ R +P+ G  + ++ IK+ GICG+D+H W  G    F  + P VLG
Sbjct: 5   NVLICQQPKELVWKQREIPIPGDNEALIKIKSVGICGTDIHAWG-GNQPFF--SYPRVLG 61

Query: 71  HESAGIVTSLGEGVIDLKVGDRVALEPGVPCGRCEMCKIGKYNLCPDMAFAATPPYDGTL 130
           HE  G +  LG+ + DLK G +VA+ P V C +C  CK G+ N C  ++       DG  
Sbjct: 62  HEICGEIVGLGKNIADLKNGQQVAVIPYVACQQCPACKSGRTNCCEKISVIGV-HQDGGF 120

Query: 131 CDYYRHSADFCYKLP-DNVSLEEGALIEPLSVGIHAARRGEVRLGDRVFVFGAGPVGLLT 189
            +Y   S      LP D +  +  ALIEP ++  HA RR  +  G++V V GAGP+GL  
Sbjct: 121 SEYL--SVPVANILPADGIDPQAAALIEPFAISAHAVRRAAIAPGEQVLVVGAGPIGLGA 178

Query: 190 AAAARAAGASHITMADISESRLKFAKSYIADETVHMTSKPPRDVDTNEFAKAEAEKLFQS 249
           AA A+A GA  + +AD S +R    + ++A         P  D    +F   +A+   Q 
Sbjct: 179 AAIAKADGA-QVVVADTSPAR----REHVATR----LELPLLDPSAEDF---DAQLRAQF 226

Query: 250 GITPANVVFDCTGVEVCVQMSVYLVKNNGKIILVGMGASVQSISVADVSAREVDVRGVMR 309
           G + A  V D TG +  +  +V L+++ G ++ VG+       S  +   +E  + G   
Sbjct: 227 GGSLAQKVIDATGNQHAMNNTVNLIRHGGTVVFVGLFKGELQFSDPEFHKKETTMMGSRN 286

Query: 310 YC-NTYPTAIEVLASEKVDLKSLITHRYKFEDSIKAFQHVKEGREGTIKVVIT 361
                +     ++A  K+    ++THRY F    + ++         IK VIT
Sbjct: 287 ATPEDFAKVGRLMAEGKITADMMLTHRYPFATLAETYERDVINNRELIKGVIT 339


Lambda     K      H
   0.319    0.136    0.405 

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: 303
Number of extensions: 18
Number of successful extensions: 5
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: 363
Length of database: 340
Length adjustment: 29
Effective length of query: 334
Effective length of database: 311
Effective search space:   103874
Effective search space used:   103874
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 (21.8 bits)
S2: 49 (23.5 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