GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Pseudomonas fluorescens GW456-L13

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 PfGW456L13_2523 Probable phenylacetic acid degradation NADH oxidoreductase paaE (EC 1.-.-.-)

Query= SwissProt::P76081
         (356 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2523
          Length = 360

 Score =  185 bits (469), Expect = 2e-51
 Identities = 118/354 (33%), Positives = 180/354 (50%), Gaps = 23/354 (6%)

Query: 6   SLTVAKVESETRDAVTITFAVPQPLQEAYRFRPGQHLTLKASFDGEELRRCYSICRSYLP 65
           SL V  V  ET DA ++   VP  L+E +R++PGQ L+ +  F G+ L RCYS+  S L 
Sbjct: 19  SLQVCAVIDETLDARSLVLDVPPALRERFRYKPGQFLSFRVPFAGKLLTRCYSMASSPLA 78

Query: 66  GEI-SVAVKAIEGGRFSRYAREHIRQGMTLEVMVPQGHFGYQPQAERQGRYLAIAAGSGI 124
             +  V VK ++GGR S +  E ++ G  LEV+ P GHF   PQA+ +   +    GSGI
Sbjct: 79  DALPKVTVKRVDGGRVSNWMNE-VQVGDWLEVLPPAGHFCLDPQADTEKPLVLFGGGSGI 137

Query: 125 TPMLAIIATTLQTEPESQFTLIYGNRTSQSMMFRQALADLKDKYPQRLQLLCIFSQETLD 184
           TP+ +I+ + L +       LIY NR   S++F+  L  L   +P +L ++ +       
Sbjct: 138 TPVFSILKSVLHSS-RRPIKLIYANRDEASVIFKDELCQLIKAHPDQLHVVHVL------ 190

Query: 185 SDLLHGRIDGEKLQSLGASLINFRLYDEAFICGPAAMMDDAETALKALGMPDKTIHLERF 244
            D + G +   +++ L    +      + FICGP   MD  E  L A+G   + IH+ERF
Sbjct: 191 -DSVQGFLTDHQVRHL----LRGSAGGDYFICGPGPFMDTVERTLLAVGEAAERIHVERF 245

Query: 245 NTPGT--------RVKRSVNVQSDGQKVTVRQDGRDREIVLNADDESILDAALRQGADLP 296
            +P           V R+  + S  + + V  DG+  EI     D ++L +    G D+P
Sbjct: 246 VSPPDPDELLAEEAVARAAAMDSQCEALIVELDGQQHEIACKPGD-TLLQSCKAAGLDVP 304

Query: 297 YACKGGVCATCKCKVLRGKVAMETNYSLEPDELAAGYVLSCQALPLTSDVVVDF 350
            +C+ G C  C C V  G+V +  N  L P ELA G+ L+CQ+ P  + V + F
Sbjct: 305 SSCEEGFCGACMCVVREGEVQLARNDVLTPKELADGWTLACQSRPTGARVRLKF 358


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: 340
Number of extensions: 12
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: 360
Length adjustment: 29
Effective length of query: 327
Effective length of database: 331
Effective search space:   108237
Effective search space used:   108237
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.

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