GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdh in Caulobacter crescentus NA1000

Align D-xylose 1-dehydrogenase (NADP(+)) 1; XDH 1; EC 1.1.1.179 (characterized)
to candidate CCNA_01283 CCNA_01283 NADP-dependent aldose oxidoreductase

Query= SwissProt::D4GP29
         (390 letters)



>FitnessBrowser__Caulo:CCNA_01283
          Length = 398

 Score =  169 bits (427), Expect = 2e-46
 Identities = 113/340 (33%), Positives = 172/340 (50%), Gaps = 21/340 (6%)

Query: 29  AMIGLGWWTRDEAIPAVEASEFCETTVVVSSSKEKAEG---ATALTESITHGLTYDEFHE 85
           A++GLG++     +P     E      +VS + EK +       + E  TH  +Y+ F  
Sbjct: 69  AILGLGYYATRIIMPRFAECEHSRLAALVSGTPEKLKTYGEQYGIPE--THRYSYETFDR 126

Query: 86  GVAADAYDAVYVVTPNGLHLPYVETAAELGKAVLCEKPLEASVERAEKLVAACDRADVPL 145
            +     D VYV+TPN LH P+ E AA  GK V+CEKP+  +V   E ++AAC +A   L
Sbjct: 127 IIDNPDVDIVYVITPNSLHRPFTERAARAGKHVMCEKPMANTVADCEAMIAACKKAGRKL 186

Query: 146 MVAYRMQTEPAVRRARELVEAGVIG---EPVFVHGHMSQRLLDEVVPDPDQWRLDPELSG 202
           M+ YR + +     A +LV  G +G     V  HG          + DP QWRL+  L+G
Sbjct: 187 MIGYRSRFQAHNIEAIKLVRDGALGPVRTVVTDHGF--------TIGDPKQWRLNRALAG 238

Query: 203 GATVMDIGLYPLNTARFVLDADPVRVRATARVD--DEAFEAVGDEHVSFGVDFDDGTLAV 260
           G ++MDIG+Y LN AR++   +PV V A    D  D  F  V ++ ++F + F  G  A 
Sbjct: 239 GGSLMDIGIYSLNAARYLTGEEPVAVNAVESTDRSDPRFGEV-EDIINFQLLFPSGATAN 297

Query: 261 CTASQSAYQLSHLRVTGTEGELEIEPA-FYNRQKRGFRLSWGDQSADYDFEQVNQMTEEF 319
           C ++ S    +  RV+G +G +EI+PA  Y  Q    +L       +   +  NQ + + 
Sbjct: 298 CVSAYSV-NCNRYRVSGPKGWVEIDPATSYQGQAMRAQLGGPPAPREPAPQPKNQFSAQL 356

Query: 320 DYFASRLLSDSDPAPDGDHALVDMRAMDAIYAAAERGTDV 359
           D+ +  +L+  +P   GD  L D+R ++AIY AA  G  V
Sbjct: 357 DHLSECILTGREPIVGGDDGLKDLRVIEAIYRAAREGRTV 396


Lambda     K      H
   0.315    0.131    0.383 

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: 344
Number of extensions: 12
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: 390
Length of database: 398
Length adjustment: 31
Effective length of query: 359
Effective length of database: 367
Effective search space:   131753
Effective search space used:   131753
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: 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