GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gci in Dyella japonica UNC79MFTsu3.2

Align D-galactarolactone cycloisomerase (EC 5.5.1.27) (characterized)
to candidate N515DRAFT_1231 N515DRAFT_1231 galactonate dehydratase

Query= BRENDA::A9CEQ8
         (378 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1231
          Length = 382

 Score =  162 bits (411), Expect = 1e-44
 Identities = 119/350 (34%), Positives = 174/350 (49%), Gaps = 19/350 (5%)

Query: 34  VEIECDDGTVGWGECL--GPARPNAAVVQAYSGWLIGQDPRQTEKIWAVLYNALRDQGQR 91
           + I+ D G  GWGE +  G A   AA V   S +LIG+DP   E +W+V+Y A   +G  
Sbjct: 18  LRIDTDAGISGWGEPVVEGRAHTVAAAVDELSDYLIGKDPHHIEDLWSVMYRAGFYRGGP 77

Query: 92  GLSLTALSGIDIALWDIKGKHYGASISMLLGGRWRESVRAYATGSFKRDNVDRVSDNASE 151
            L ++A++GID ALWDIKGK  G  +  LLGG  R+ +R Y+         DR +D A  
Sbjct: 78  IL-MSAIAGIDQALWDIKGKDLGRPVYDLLGGPVRDRIRVYSW-----IGGDRPADTARA 131

Query: 152 MAERRAEGFHACKIKI--------GFG-VEEDLRVIAAVREAIGPDMRLMIDANHGYTVT 202
             E  A GF A K+           F  VE  L  + AVR+A+GP + L +D +      
Sbjct: 132 AMEAVARGFTAVKMNATEEMQYVDSFDKVERVLANVQAVRDAVGPHVGLGLDFHGRVHKP 191

Query: 203 EAITLGDRAAGFGIDWFEEPVVPEQLDAYARVRAGQPIPVAGGETWHGRYGMWQALSAGA 262
            A  L      + + + EEPV+ E L+    + +  P P+A GE  + RY   + L  G 
Sbjct: 192 MAKVLMRELEPYKLMFIEEPVLSEYLECIPELASISPAPIALGERLYSRYDFKRVLETGG 251

Query: 263 VDILQPDLCGCGGFSEIQKIATLATLHGVRIVPHVWGTGVQIAAALQFMAAMTPDPVRVN 322
           VDILQPD    GG +E +KIA +A  + V I  H     + +AA LQ  A      ++  
Sbjct: 252 VDILQPDPSHAGGITETRKIAAMAEAYDVAIALHCPLGPIALAANLQIDAVSHNAFIQEQ 311

Query: 323 PIEPIMEFDRTHNPFRQAVLREPLEAVNGVVTIPDGPGLGIEINRDALTE 372
            +   + ++ +++       R      +G VT+P GPGLGI +N + + E
Sbjct: 312 SLG--IHYNASNDLLDYVSDRSVFAYQDGYVTMPTGPGLGITVNEEYVAE 359


Lambda     K      H
   0.321    0.138    0.431 

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: 424
Number of extensions: 20
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: 378
Length of database: 382
Length adjustment: 30
Effective length of query: 348
Effective length of database: 352
Effective search space:   122496
Effective search space used:   122496
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 (21.9 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