GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Pseudomonas stutzeri RCH2

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate GFF3998 Psest_4071 4-hydroxyphenylpyruvate dioxygenase and related hemolysins

Query= BRENDA::P80064
         (357 letters)



>FitnessBrowser__psRCH2:GFF3998
          Length = 641

 Score =  190 bits (482), Expect = 1e-52
 Identities = 117/328 (35%), Positives = 166/328 (50%), Gaps = 11/328 (3%)

Query: 12  GFEFIELASPTPNT--LEPIFEIMGFTKVATHRSKDVHLYRQGAINLILNNEPHSVASYF 69
           G +F+E A   P+   L    + +GF  V  HRSKDV L+RQG IN++LN EP+S A  +
Sbjct: 296 GIDFLEFAVDEPHAVRLGSWLQQLGFAHVGQHRSKDVQLFRQGEINIVLNAEPYSFAHNY 355

Query: 70  AAEHGPSVCGMAFRVKDSQKAYKRALELGAQPIHIETGPMELNLPAIKGIGGAPLYLIDR 129
              HGPSVC MA ++ D   A  RA   G QP     GP E  +PA++   G  +YL++ 
Sbjct: 356 FEAHGPSVCAMALKIDDEASALARACAFGGQPYRGLIGPNERQIPAVRAPDGGLIYLLES 415

Query: 130 FGEGSSIYDIDFVFLEGVDRHPVGAGLKIIDHLTHNVYRGRMAYWANFYEKLFNFREIRY 189
              G S YDIDF  L  V   P GAGL+ IDH+   +    +A W  FY  LF+F     
Sbjct: 416 GAPGQSNYDIDF-RLHAVT--PAGAGLQRIDHMATALPAESLASWVLFYRSLFDFEADDE 472

Query: 190 FDIKGEYTGLTSKAMTAPDGMIRIPLNEESSKGAGQIEEFLMQFNGEGIQHVAFLSDDLI 249
             +   Y  +  +AM +P G +R+PLN    +    I + L  + G G+ HVAF  DD+ 
Sbjct: 473 LLLPDPYGLMKCRAMRSPCGRVRLPLNTSQDRDT-VIAQALSSYRGAGVHHVAFACDDIF 531

Query: 250 KTWDHLKSIGMRFMTAPPDTYYEMLEGRLPNHGEPVGELQARGILLDGSSESGDKRLLLQ 309
                 ++ G+  +  P + YY+ L  R       + EL    +L D  +E G+   L  
Sbjct: 532 AEVARAQAAGVPLLQIPRN-YYDDLAARFDFDDSLLAELARYNVLYDRDAEGGE---LFH 587

Query: 310 IFSETLMGPVFFEFIQR-KGDDGFGEGN 336
           +++E   G  FFE +QR  G  G+G  N
Sbjct: 588 VYTEPFEGRFFFEILQRCNGYAGYGTPN 615


Lambda     K      H
   0.321    0.141    0.420 

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: 595
Number of extensions: 36
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: 357
Length of database: 641
Length adjustment: 33
Effective length of query: 324
Effective length of database: 608
Effective search space:   196992
Effective search space used:   196992
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 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