GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Sphingomonas koreensis DSMZ 15582

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate Ga0059261_3340 Ga0059261_3340 Predicted oxidoreductases (related to aryl-alcohol dehydrogenases)

Query= BRENDA::F2YCN5
         (340 letters)



>FitnessBrowser__Korea:Ga0059261_3340
          Length = 351

 Score =  138 bits (348), Expect = 2e-37
 Identities = 98/315 (31%), Positives = 161/315 (51%), Gaps = 16/315 (5%)

Query: 24  TRVALGTWAI--GGWMWG--GTDDDASIKTIHRAIDLGINIIDTAPAYGRGHAEEVVGKA 79
           +R++LGT     GG +     TD   +   +  A+  GIN IDTA  Y    +EE++GK 
Sbjct: 14  SRLSLGTMTFTRGGGLKAIAKTDLKDAAALVDHALAAGINFIDTADVYSDFESEEMLGKI 73

Query: 80  IKGQRDNLIIATKVGLDWTLTPDQSMRRNSSASRIKKEIEDSLRRLGTDYIDLYQVHWPD 139
           + G+RD L+IATK G  W  T     R   SA+ +   I+ SL+RLGTD++D+Y  H  D
Sbjct: 74  VAGRRDELVIATKAG--WR-TGQPLNRSGLSAAHLHWSIDHSLKRLGTDHVDVYIAHRDD 130

Query: 140 PLVPIEETATILEALRKEGKIRSIGVSNY------SVQQMDEFKKYAELAVSQSPYNLFE 193
              P+EET   L+A+ + GK R +GVSN+      +  ++     +A    +Q  Y+L  
Sbjct: 131 RNTPLEETLQALDAIVRAGKARYLGVSNWPAWKVAAAIELQRANGWAPFTHAQMLYSLMH 190

Query: 194 REIDKDILPYAKKNDLVVLGYGALCRGLLSGRMTADRAFTGDDLRKTDPKFQKPRFEHYL 253
           R+I+++ LP A++  L +  +  L  G L+G+ T D A   DD   +       R   Y 
Sbjct: 191 RDIEQEFLPMARRYGLGITPWSPLGGGFLTGKYTRDNAGGADDRLASHDDIPLDREMGY- 249

Query: 254 AAVEELKKLAKEHYNKSVLALAIRWMLEQGPTLA-LWGACKPEQIDGIDEVFGWQISDED 312
             ++ ++ +A  H   S+  +A+ W+L +    + L GA K  Q+D        ++SD++
Sbjct: 250 KLIDTMRGIADGH-GVSIAQIALAWLLSKDQVSSILLGATKLHQLDDNLAAVNVKLSDDE 308

Query: 313 LKQIDAILAKNIPNP 327
           +  ++ I A+    P
Sbjct: 309 IAAMEEISAQRRAYP 323


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: 319
Number of extensions: 20
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: 351
Length adjustment: 29
Effective length of query: 311
Effective length of database: 322
Effective search space:   100142
Effective search space used:   100142
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: 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