GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA3 in Alicycliphilus denitrificans K601

Align L-rhamnonate dehydratase (EC 4.2.1.90) (characterized)
to candidate WP_013721158.1 ALIDE2_RS00485 mandelate racemase/muconate lactonizing enzyme family protein

Query= metacyc::MONOMER-16232
         (397 letters)



>NCBI__GCF_000204645.1:WP_013721158.1
          Length = 387

 Score =  108 bits (270), Expect = 3e-28
 Identities = 106/361 (29%), Positives = 158/361 (43%), Gaps = 35/361 (9%)

Query: 62  LVVEIEAEDGTVGF--AVTTGGEPAAYIVEKHLARFLEGRAPTDYEKIWDQMYFSTQYYG 119
           + V I  +DGTVG+  A T G   AA +  +  A +LEG+     E  W+ M+  + +  
Sbjct: 15  MFVRITTDDGTVGYGEAGTWGHIEAAGVCIRRFAEYLEGKDAFAIEHHWNVMHRFSYF-- 72

Query: 120 RKGLVVNA-ISGVDLALWDLLGKLRQEPVYHLLGGAVRDELQFYATGARPDKAKEFGFIG 178
             GL  NA IS +D+ALWD+ GK    P+Y LLGGA R + + Y         K      
Sbjct: 73  -TGLAENAAISAIDIALWDIKGKALNVPIYELLGGAARTKARIYGHIYENSIEKMLVECQ 131

Query: 179 GKMPL------HHGPA--EGVEGL--KKNIAELAD-------MRSKVGDDFWLMWDCWMA 221
            KM        H  P   EG + +  K +I ++ D       MR  VGD   L+ +    
Sbjct: 132 AKMEAGFNAFGHLNPFLDEGNDQVYFKTHIKKMRDAIDNTRRMREVVGDRVDLLIEIHRR 191

Query: 222 LDVDYATRLAIAAHDFGLKWIEEAISPDDYWGYQQLKRNVPKGMLVTTGEHEATRWGFRM 281
           L    A   A    D    +IE+ I P+   G  ++   +  G+ + TGE  A  + F+ 
Sbjct: 192 LTPAEAIVFARGIEDTHPMFIEDPIRPEGPDGMARVAEKI--GIPIATGERFANLYEFQT 249

Query: 282 LMEMDCCDIIQPDVGWCGGVTELLKISALADAHGKMVVPHGSSVYSYHFVITRHNSPFAE 341
           LM     +  + D+  CGG+T   K++ALA+AH   VVPH            + ++    
Sbjct: 250 LMARGGVEYARVDLCLCGGITGAKKVAALAEAHHVQVVPHNPLSPIGLAACLQLDAAIPN 309

Query: 342 FLMMHPGPTEVVPMF--HPQLLGE------PVPDNGRMKVSALDKPGFGVDLNPDIAMHR 393
           F +          +F   P+ LG       P+PD G + +     PG G++L PD    R
Sbjct: 310 FAIQEYATGFEAGIFESRPEHLGSDIVDQVPLPDAGFVDIPT--GPGLGMNLLPDAQKIR 367

Query: 394 P 394
           P
Sbjct: 368 P 368


Lambda     K      H
   0.322    0.140    0.451 

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: 436
Number of extensions: 23
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: 397
Length of database: 387
Length adjustment: 31
Effective length of query: 366
Effective length of database: 356
Effective search space:   130296
Effective search space used:   130296
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 24 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