GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Azohydromonas australica DSM 1124

Align 4-hydroxyphenylpyruvate dioxygenase; 4HPPD; HPD; HPPDase; EC 1.13.11.27 (uncharacterized)
to candidate WP_028999745.1 H537_RS0123135 sugar phosphate isomerase/epimerase and 4-hydroxyphenylpyruvate domain-containing protein

Query= curated2:Q9I576
         (357 letters)



>NCBI__GCF_000430725.1:WP_028999745.1
          Length = 637

 Score =  146 bits (368), Expect = 2e-39
 Identities = 102/341 (29%), Positives = 160/341 (46%), Gaps = 12/341 (3%)

Query: 17  GFEFVEFTAPDAKGIEQLRQLFNMMGFTETAKHRSKEVFLFQQNDINIVLNGSPTGHVHE 76
           G  F+EF A D    E L  L   +GF    +HRSK V LF+Q  +N+VLN   T    E
Sbjct: 301 GLSFIEF-AVDGAHAEALGHLVRQLGFRFAGRHRSKAVTLFRQGGVNLVLNQQATPAARE 359

Query: 77  FALKHGPSACAMAFRVKNASQAAAYAESQGAKLVGSHANFGELNIPSLEGIGGSLLYLVD 136
                GPS CA+  R  +   A   A +  +    +    GE  +PS+   GG +L+ VD
Sbjct: 360 RFSLQGPSVCALGLRTDDPVGALNRATALQSARYDAPTGTGEQRLPSIVAPGGIVLHFVD 419

Query: 137 R-YGDRSIYDVDFEFIEGRSANDNSVGLTYIDHLTHNVKRGQMDVWSGFYERIANF---R 192
              G+  +++ DF      +      GL  IDHL   +   ++D W  F   +       
Sbjct: 420 EALGENGLFEKDFILEPEAAEGAGGAGLECIDHLAVGLTADRLDTWVLFCRAVLGLDAGD 479

Query: 193 EIRYFDIEGKLTGLFSRAMTAPCGKIRIPINESADDTSQIEEFIREYHGEGIQHIALTTD 252
            +++ D  G +    S  M+     +R+ +N S  + +++ +  +   G G+QHIA    
Sbjct: 480 AVKFADPFGLIR---STGMSDAARHLRLVLNMSMSERTRMAQAAQASGGVGVQHIAFGCS 536

Query: 253 DIYATVRKLRDNGVKFMSTPDTYYEKVDTRVAGHGEPLEQLRELNLLIDGAPGDDGILLQ 312
           D++A V KLR  GV+F+   D YY+ + TR     E +++LR   +L D +P   G  L 
Sbjct: 537 DLFAAVDKLRRAGVRFVPISDNYYDDLPTRFEVAPELVQRLRAAGVLFDRSP--QGDYLH 594

Query: 313 IFTDTVIGP-IFFEIIQRKGN-QGFGEGNFKALFESIEEDQ 351
            +T+   G   FFE++QR G   G+G  N  A   S  +++
Sbjct: 595 AYTEGYAGAGFFFELVQRLGGYDGYGAVNAPARMASQAQEE 635


Lambda     K      H
   0.320    0.139    0.406 

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: 527
Number of extensions: 25
Number of successful extensions: 3
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: 637
Length adjustment: 33
Effective length of query: 324
Effective length of database: 604
Effective search space:   195696
Effective search space used:   195696
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