GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Pseudomonas benzenivorans DSM 8628

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 WP_090440011.1 BLS63_RS03815 ferredoxin:oxidoreductase FAD/NAD(P)-binding protein

Query= SwissProt::P76081
         (356 letters)



>NCBI__GCF_900100495.1:WP_090440011.1
          Length = 516

 Score =  190 bits (483), Expect = 6e-53
 Identities = 125/350 (35%), Positives = 183/350 (52%), Gaps = 22/350 (6%)

Query: 4   FHSLTVAKVESETRDAVTITFAVPQPLQEAYRFRPGQHLTLKASFDGEELRRCYSICRSY 63
           F  L V   + E+ DA + T  VP  LQE +  RPGQ LTLK       L RCYS+ +  
Sbjct: 186 FAGLEVGGRQVESADACSFTLRVPADLQERFAARPGQFLTLKVPCAEPPLLRCYSLSQLP 245

Query: 64  LPGE-ISVAVKAIEGGRFSRYAREHIRQGMTLEVMVPQGHFGYQPQAERQGRYLAIAAGS 122
             GE + + VK + GGR S +  +H++ G  +EV+ P G F      +  G  L + AGS
Sbjct: 246 QVGEPLRITVKRVAGGRASNWLFDHLQPGDHIEVLPPAGVF---VPRDLTGDLLLLGAGS 302

Query: 123 GITPMLAIIATTLQTEPESQFTLIYGNRTSQSMMFRQALADLKDKYPQRLQLLCIF--SQ 180
           GITP++AI+   L  + + +  L Y NR + S++F   L  L+ +YPQRLQL   F  SQ
Sbjct: 303 GITPLMAILQAAL-AQGQGRVCLFYANRDAGSVIFADELKGLQRRYPQRLQLRYWFDASQ 361

Query: 181 ETLDSDLLHGRIDGEKLQSLGASLINFRLYDEAFICGPAAMMDDAETALKALGMPDKTIH 240
              ++D + G I   +               E FICGP   MD A  AL  LG+ ++ I 
Sbjct: 362 GVPEADAIAGEIADWREA-------------ECFICGPQPFMDGARAALLGLGVIEQRIR 408

Query: 241 LERFNTPGTRVKRSVNVQSDGQKVTVRQDGRDREIVLNADDESILDAALRQGADLPYACK 300
           LERF        R+    S   ++ V  +GR  E+ +    E +L+A  + G   P AC+
Sbjct: 409 LERFAAQPVSPLRAAKA-SRPSRLRVTLNGRRHELDVQRG-EMLLEAMEQAGLQPPNACR 466

Query: 301 GGVCATCKCKVLRGKVAMETNYSLEPDELAAGYVLSCQALPLTSDVVVDF 350
            GVCA CKC+V+ G V M +N +L   ++  G+VL+CQA P + ++ V++
Sbjct: 467 SGVCAACKCRVVSGSVTMRSNQALSEQQVRQGWVLACQAEPSSVELQVEY 516


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: 410
Number of extensions: 18
Number of successful extensions: 6
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: 516
Length adjustment: 32
Effective length of query: 324
Effective length of database: 484
Effective search space:   156816
Effective search space used:   156816
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: 51 (24.3 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