GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Phaeobacter inhibens BS107

Align ring 1,2-phenylacetyl-CoA epoxidase PaaE subunit (EC 1.14.13.149) (characterized)
to candidate GFF393 PGA1_c04040 phenylacetic acid degradation NADH oxidoreductase PaaE

Query= metacyc::MONOMER-15950
         (357 letters)



>FitnessBrowser__Phaeo:GFF393
          Length = 357

 Score =  353 bits (905), Expect = e-102
 Identities = 174/358 (48%), Positives = 238/358 (66%), Gaps = 3/358 (0%)

Query: 1   MSKFHSLTIKEVRPETRDAVSIAFDVPAELADSFRFTQGQHLVMRTQLDGEEVRRSYSIC 60
           M++FH L + +VR   RDAV +        A+ F FTQGQ+L  R   DGEE+RRSYSIC
Sbjct: 1   MARFHDLVVTDVRKTIRDAVVVTLKPVGGAAEEFDFTQGQYLTFRRDFDGEELRRSYSIC 60

Query: 61  TGVNDGELRVAIKRVAGGRFSAYANESLKAGQRLEVMPPSGHFHVELDAARHGNYLAVAA 120
            G ++G L+V IKRV GG FS +AN  LKAG  L+ M P G F   L+ A   +YL  A 
Sbjct: 61  AGKDEGILQVGIKRVDGGAFSTWANTELKAGDTLQAMAPMGSFFTPLNEAAEKHYLGFAG 120

Query: 121 GSGITPILSIIKTTLETEPHSRVTLLYGNRSSASTLFREQLEDLKNRYLQRLNLIFLFSR 180
           GSGITP+LSI+KTTL  EP++  TL+Y N+   + +FRE+LEDLKN Y+ R NLI +   
Sbjct: 121 GSGITPVLSILKTTLAAEPNASFTLVYANKGVNTIMFREELEDLKNLYMGRFNLIHVLES 180

Query: 181 EQQDVDLYNGRIDADKCGQLFSRWIDVKALDAAFICGPQAMTETVRDQLKANGMAAERIH 240
           + Q++DL+ G +  +KC QLF RWID+K++D AFICGP+ M   +   L+  G+   +I 
Sbjct: 181 DAQEIDLFTGLVTEEKCAQLFERWIDIKSVDTAFICGPEPMMLGIASALRTAGLNDSQIK 240

Query: 241 FELFAAA--GSAQKREARESAAQDSSVSQITVISDGRELSFELPRNSQSILDAGNAQGAE 298
           FELFA+A  G A+++         ++ ++  +  DG   + E+ ++  ++LDA      +
Sbjct: 241 FELFASAQPGRAKRKVTAGGTGTGANQTKAAITLDGATQTIEIGKD-MTLLDAALENAMD 299

Query: 299 LPYSCKAGVCSTCKCKVVEGEVEMDSNFALEDYEVAAGYVLSCQTFPISDKVVLDFDQ 356
            PY+CKAGVCSTC+CKV+EGEVEM +N ALEDYEV  GYVLSCQ +P+SDKVV+D+DQ
Sbjct: 300 APYACKAGVCSTCRCKVLEGEVEMIANHALEDYEVEKGYVLSCQAYPLSDKVVVDYDQ 357


Lambda     K      H
   0.319    0.133    0.377 

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: 350
Number of extensions: 14
Number of successful extensions: 2
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: 357
Length of database: 357
Length adjustment: 29
Effective length of query: 328
Effective length of database: 328
Effective search space:   107584
Effective search space used:   107584
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 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