GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA3 in Pedobacter sp. GW460-11-11-14-LB5

Align L-rhamnonate dehydratase; RhamD; EC 4.2.1.90 (uncharacterized)
to candidate CA265_RS12250 CA265_RS12250 enolase

Query= curated2:A9BQY2
         (395 letters)



>FitnessBrowser__Pedo557:CA265_RS12250
          Length = 388

 Score =  141 bits (355), Expect = 4e-38
 Identities = 111/369 (30%), Positives = 176/369 (47%), Gaps = 34/369 (9%)

Query: 43  PEYRQSRRSFGI--NVLGTLVVEIEDSA----GRVGFAVTTGGEPAAYI--VEKHLARFL 94
           PE +Q    +G+  +   TLVV   DS     G    AV + G  A+ +  +E  L   L
Sbjct: 16  PEAKQHVSDYGLLTSFDMTLVVITTDSGLQGFGEAKAAVGSCGICASIVNCIENELKPML 75

Query: 95  EGARVTDIERIWDQMYLSTLYY------------GRKGIVINTISGVDLALWDLLGKVRG 142
            G  V +I R+W++MY  T  +            GR+G+ I+ +SG+D ALWDL GK+  
Sbjct: 76  LGKSVKNITRLWEEMYNGTRDHYALSRGRKFPILGRRGLTISAMSGIDTALWDLKGKMLN 135

Query: 143 EPVHQLLGGAVRDELQFYATGARPDL----AQKMGFIG-GKMPLHHGPAEGEEGLRRNLQ 197
            PV  LLGGA R ++  YA+G   D      Q MG++  G   +       ++ +++++ 
Sbjct: 136 VPVADLLGGACRTKMPAYASGGWADEQNIGEQLMGYVNKGFKGVKMRVGVMDDTVQKSIN 195

Query: 198 ELATMRERVGPDFWLMLDCWMSLDVNYATRLAQGAQAHGLKWIEEALPPDDYWGYAALRK 257
            +   R  +GPD  LM+D   +  V  A +  +G +   + W EE + PD+  G A +R 
Sbjct: 196 RVKAARAALGPDIKLMVDAHGTFSVPEAKQFCRGVEDCNVYWFEEPISPDNRKGTAEVR- 254

Query: 258 NVPTGMLVTTGEHEATRWGFRQLLEMGCCDIIQPDVGWCGGITELLKISALADAHQALVI 317
              T + +  GE E T +    LL++   D++QPD    GGI+E +++S LA  HQ  + 
Sbjct: 255 -AATDIPIAAGESEFTSFDIHDLLQIRAIDVVQPDAAIIGGISEAMRVSHLASVHQVELA 313

Query: 318 PH--GSSVYSYHFVATRHNSPFAEFLMMAPKADEVVPMFHPQLLGEPVPVNGRMRLSALD 375
           PH  GS+      +     S  A  +  +   +   PM +  +  +   VNG   +SA  
Sbjct: 314 PHCWGSAFSFMAGLTVAFASASATIIEFSLGGN---PMMYDLVNEQIAVVNG--EISAPT 368

Query: 376 RPGFGVELN 384
            PG G+  N
Sbjct: 369 APGLGLTPN 377


Lambda     K      H
   0.322    0.139    0.442 

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: 401
Number of extensions: 25
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: 395
Length of database: 388
Length adjustment: 31
Effective length of query: 364
Effective length of database: 357
Effective search space:   129948
Effective search space used:   129948
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.

Links

Downloads

Related tools

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