GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Dinoroseobacter shibae DFL-12

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate 3607117 Dshi_0539 aldo/keto reductase (RefSeq)

Query= BRENDA::F2YCN5
         (340 letters)



>FitnessBrowser__Dino:3607117
          Length = 312

 Score =  107 bits (266), Expect = 5e-28
 Identities = 96/317 (30%), Positives = 140/317 (44%), Gaps = 45/317 (14%)

Query: 34  GGWMWGGT-DDDASIKTIHRAIDLGINIIDTAPAYGRGHAEEVVGKAIKGQRDNLIIATK 92
           G   +GGT D  AS          GIN  DTA  Y  G +E  +G+ +  Q D+L+IATK
Sbjct: 18  GCMQFGGTADKPASAAMFEACRAAGINFFDTAHVYTEGRSETWLGEMVTDQADDLLIATK 77

Query: 93  VGLDWTLTPDQSMRRNSSASRIKKEIEDSLRRLGTDYIDLYQVHWPDPLVPIEETATILE 152
           VG              S  + I+   ++SLRRLG D +D+  +H  D   P+EET   L 
Sbjct: 78  VGYVG----------GSGRANIRTTFDESLRRLGLDAVDILYLHRWDAETPLEETFEALA 127

Query: 153 ALRKEGKIRSIGVSNYSVQQMDEFKKYAE-----LAVSQSPYNLFEREIDKDILPYAKKN 207
            L+  G+ R IGVSN++  Q+ + +  AE     + + Q  Y+L +R+ + +ILP A   
Sbjct: 128 DLQSAGRFRYIGVSNFAAWQVMKAQAVAEQFGTRIDILQPMYSLIKRQAEVEILPMALSE 187

Query: 208 DLVVLGYGALCRGLLSGRMTADRAFTGDDLRKTDPKFQKPRFEHYLAAVEELKKLAKEHY 267
            + V  Y  L  GLL+G+          +  K + ++  P       A   L+ LA E  
Sbjct: 188 GIAVAPYSPLGGGLLTGKYAEGGTGRLTENEKYEMRYSMPWMHE---AAVALRVLAAE-I 243

Query: 268 NKSVLALAIRWMLEQGPTLALWGACKPEQIDGIDEVFGWQISDEDLKQIDAILAKN---I 324
             +   LA+            W A  P    G+       IS  D+ Q+DA LA     +
Sbjct: 244 GAAPATLAV-----------AWAAAHP----GVKAPI---ISARDVAQLDASLAARDMAL 285

Query: 325 PNPIGAEFMA----PPP 337
           P  + A   A    PPP
Sbjct: 286 PPDLYARITALSQTPPP 302


Lambda     K      H
   0.317    0.136    0.407 

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: 247
Number of extensions: 12
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: 340
Length of database: 312
Length adjustment: 28
Effective length of query: 312
Effective length of database: 284
Effective search space:    88608
Effective search space used:    88608
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