GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Pseudomonas benzenivorans DSM 8628

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate WP_090448693.1 BLS63_RS26010 4-hydroxyphenylpyruvate dioxygenase

Query= reanno::pseudo3_N2E3:AO353_26925
         (358 letters)



>NCBI__GCF_900100495.1:WP_090448693.1
          Length = 635

 Score =  174 bits (440), Expect = 8e-48
 Identities = 109/328 (33%), Positives = 164/328 (50%), Gaps = 11/328 (3%)

Query: 13  GFEFIELA--SPTPNTLEPIFEIMGFTKVATHRSKDVHLYRQGQINLILNNEPHSVASYF 70
           G EF+E A        L    E +GF +   HRSKDV L RQG IN++LN EP+S A  F
Sbjct: 295 GVEFLEFAVDEAVGARLGDWLERLGFARAGQHRSKDVSLLRQGDINIVLNAEPYSFAHNF 354

Query: 71  AAEHGPSVCGMAFRVKDSQKAYKRALELGAQPIHIETGPMELNLPAIKGIGGAPLYLIDR 130
              HGPS+C  A RVKD   A +RA +   QP     GP E  +PA++   G+ +YL+++
Sbjct: 355 FEAHGPSLCATALRVKDGAAALQRACDYRGQPYRGLVGPNEREIPAVRAPDGSLIYLVEQ 414

Query: 131 FGEGSSIYDIDFVFIEGVDRHPVGAGLKIIDHLTHNVYRGRMAYWANFYEKLFNFREIRY 190
            G G +IYD DF    G +      GL+ IDH+   +    +  W  FY+ + +F     
Sbjct: 415 AGAGQTIYDSDFSLDAGAE---AKGGLQRIDHMALALPADGLDSWVLFYKSVLDFEADDE 471

Query: 191 FDIKGEYTGLTSKAMTAPDGMIRIPLNEESSKGAGQIEEFLMQFNGEGIQHVAFLSDDLI 250
             +   Y  + S+A+ +    +R+PLN   ++    I   L  + G G+ H+AF   D+ 
Sbjct: 472 VVLPDPYGLVKSRALRSRCSSVRLPLNISENRNTA-IAHALSSYRGSGVHHIAFSCADIF 530

Query: 251 KTWDHLKKIGMRFMTAPPDTYYEMLEGRLPNHGEPVNELQARGILLDGSSEAGDKRLLLQ 310
           +     K+ G+  +  P + YY+ L  R     E ++EL    +L D  ++ G+   L  
Sbjct: 531 QEVARAKEAGVPLLEIPLN-YYDDLAARFDFDDEFLSELAYYNVLYDRDAQGGE---LFH 586

Query: 311 IFSETLMGPVFFEFIQRK-GDDGFGEGN 337
           +++E      FFE IQRK G  G+G  N
Sbjct: 587 VYTEAFEERFFFEIIQRKNGYVGYGAAN 614


Lambda     K      H
   0.321    0.141    0.419 

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: 557
Number of extensions: 35
Number of successful extensions: 4
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: 358
Length of database: 635
Length adjustment: 33
Effective length of query: 325
Effective length of database: 602
Effective search space:   195650
Effective search space used:   195650
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