GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Sinorhizobium fredii NGR234

Align 1,2-phenylacetyl-CoA epoxidase, subunit E; 1,2-phenylacetyl-CoA epoxidase, reductase subunit; 1,2-phenylacetyl-CoA monooxygenase, subunit E; EC 1.-.-.- (characterized)
to candidate YP_002827141.1 NGR_c26310 dioxygenase reductase subunit

Query= SwissProt::P76081
         (356 letters)



>NCBI__GCF_000018545.1:YP_002827141.1
          Length = 368

 Score =  132 bits (331), Expect = 2e-35
 Identities = 106/345 (30%), Positives = 157/345 (45%), Gaps = 18/345 (5%)

Query: 7   LTVAKVESETRDAVTITFAVPQPLQEAYRFRPGQHLTLKASFDGEELRRCYSICRS-YLP 65
           L    V  E  D  T TFAV       + + PGQ +T++    G +L R Y++  S   P
Sbjct: 28  LVCTSVTDEAPDVKTFTFAVEGG--GWFNYMPGQFITVELRAKGGDLHRTYTVSSSPSRP 85

Query: 66  GEISVAVKAIEGGRFSRYAREHIRQGMTLEVMVPQGHFGYQPQAERQGRYLAIAAGSGIT 125
             I++ +KA      +R+  E++R G  +    P GHF       +  +YL I+AGSGIT
Sbjct: 86  YAIAITIKAQPTSIGTRWMFENVRSGSRVRAYGPSGHFTLSRNPGK--KYLFISAGSGIT 143

Query: 126 PMLAIIATTLQTEPESQFTLIYGNRTSQSMMFRQALADLKDKYPQRLQLLCIFSQETLDS 185
           PM++++       P+     I   R  + ++FR+ L  L  + P  L L  +    ++ S
Sbjct: 144 PMMSMLRWLSDCAPDIDVVFINSARRPEEIIFREELELLAKRMPN-LSLGFLPEARSVAS 202

Query: 186 DL--LHGRIDGEKLQSLGASLINFRLYDEAFICGPAAMMDDAETALKALGMPDKTIHLER 243
               L GRID  KL  L    +      E F CGP   M      ++A G      H E 
Sbjct: 203 PWAGLMGRIDRHKLSMLTPDFMG----REIFCCGPDPFMRAVSAIVRAEGFDMGHYHQES 258

Query: 244 FNTPG---TRVKRSVNVQSDGQK--VTVRQDGRDREIVLNADDESILDAALRQGADLPYA 298
           F       T  K++  +  DG+   VTV   G + E V     ++IL+ A   G  +P A
Sbjct: 259 FGATSIAETVHKQAREIVLDGKPTGVTVSFLGSNEEQVCEPG-KTILETARAAGVRIPAA 317

Query: 299 CKGGVCATCKCKVLRGKVAMETNYSLEPDELAAGYVLSCQALPLT 343
           C+ G+C TCK     G+V M  N  +   E+ AGYVL+C + P T
Sbjct: 318 CESGICGTCKVLKRSGEVVMHHNGGISDQEINAGYVLACCSRPTT 362


Lambda     K      H
   0.320    0.135    0.390 

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: 324
Number of extensions: 20
Number of successful extensions: 5
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: 356
Length of database: 368
Length adjustment: 29
Effective length of query: 327
Effective length of database: 339
Effective search space:   110853
Effective search space used:   110853
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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