GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdh in Sinorhizobium meliloti 1021

Align D-xylose 1-dehydrogenase (NADP+) (EC 1.1.1.179) (characterized)
to candidate SMc00375 SMc00375 oxidoreductase

Query= BRENDA::D4GP30
         (325 letters)



>FitnessBrowser__Smeli:SMc00375
          Length = 328

 Score =  167 bits (423), Expect = 3e-46
 Identities = 117/323 (36%), Positives = 160/323 (49%), Gaps = 9/323 (2%)

Query: 1   MMFGILGTAGIGVKSVIPAVQASEH-EAAAIASRDEARASAVADELGIPTAYGSYEALLA 59
           + FGIL TA IG + V+PA+Q +E+    AIASRD A+A A+AD   +P A+GSYE +LA
Sbjct: 2   LRFGILSTAKIGRELVVPAIQDAENCVVTAIASRDLAKARAMADRFSVPHAFGSYEEMLA 61

Query: 60  DDSLDAVYIPLPNGLHADWVRAAADRGLHVLCEKPLTASADETAAVFDYCEDAGVTLMEA 119
            D++DAVYIPLP   H +W   AAD G HVLCEKPL   A+E  AV    E   V + EA
Sbjct: 62  SDTVDAVYIPLPTSQHVEWAIKAADAGKHVLCEKPLALKAEEIDAVIAARERNKVLISEA 121

Query: 120 FMYRFHPLTERAAELVA-SELGAVVSVTSNFSFRLPDGADDIRIDPDLAGGSVMDVGCYA 178
           +M  + P+  +   L+A   +G +  V   F++   D   ++R  P L GG + D+G Y 
Sbjct: 122 YMVTYSPVWRKVRSLIAEGAIGRLRHVQGAFTYYNRD-PGNMRNVPSLGGGGLPDIGVYP 180

Query: 179 VSAARLFLG-TPDRVYATTTDTRDCGVDTRMSGVLEY-DSGATARVESSFDTPETQYYRV 236
               R   G  P RV A T    + G D   S   ++ D   +  + +     +   +  
Sbjct: 181 AITTRFSTGKEPLRVQANTERDPEFGTDVYSSVRADFGDFELSFYISTQLAARQVMVF-- 238

Query: 237 QTTDGRLEANPAFNVD--PTAAAELTYATDGRVVTETFDPTDSYRREVEAFARAVETGET 294
               G +E    FN D       ELT    G+     F     Y+ E EAFARA +    
Sbjct: 239 HGDKGYIEVKSPFNADRYGREEVELTNQNHGQSQLFRFQDARQYKLEAEAFARAAKGEAE 298

Query: 295 PRVDREESVSVMRTIDAIYESAE 317
             V  E S      IDAIY ++E
Sbjct: 299 DVVTLENSRLNQMFIDAIYRASE 321


Lambda     K      H
   0.316    0.131    0.371 

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: 241
Number of extensions: 15
Number of successful extensions: 4
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: 325
Length of database: 328
Length adjustment: 28
Effective length of query: 297
Effective length of database: 300
Effective search space:    89100
Effective search space used:    89100
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 (21.6 bits)
S2: 48 (23.1 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