GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK' in Pseudomonas simiae WCS417

Align Triokinase/FMN cyclase; Bifunctional ATP-dependent dihydroxyacetone kinase/FAD-AMP lyase (cyclizing); EC 2.7.1.28; EC 2.7.1.29; EC 4.6.1.15 (characterized)
to candidate GFF2361 PS417_12040 dihydroxyacetone kinase

Query= SwissProt::Q4KLZ6
         (578 letters)



>FitnessBrowser__WCS417:GFF2361
          Length = 333

 Score =  179 bits (453), Expect = 2e-49
 Identities = 107/326 (32%), Positives = 171/326 (52%), Gaps = 9/326 (2%)

Query: 5   KMVNSVEGCAGDALAGFVACNPDLQLLQGYRVALRSDLDSLKGRVALLSGGGSGHEPAHA 64
           +++N  +    D L G +  +P+L+  +     +     S  GRV +++GGGSGHEPA  
Sbjct: 3   RVINDPDQVVEDMLRGILVAHPELRQYETNPRVIVKAKPSGPGRVGIVTGGGSGHEPAFL 62

Query: 65  GFIGKGMLTGVIAGAVFASPAVGSILAAIRAVAQAGTAGTLLIVKNYTGDRLNFGLAMEQ 124
           G++G G++  V  G +F+SP   S   A RA      AG   +  NY GD +N  LAM+ 
Sbjct: 63  GYVGPGLVDAVAVGEIFSSPTAKSFFDAFRAADHG--AGVACLYGNYAGDNMNVKLAMKM 120

Query: 125 AKAEGISVEMVVIEDDSAFTVLKK-AGRRGLCGTILIHKVAGALAEEGMGLEEITKKVSV 183
           A ++ + +  VV  DD A     + A RRG+ G I + K+ GA A +   L+ + +    
Sbjct: 121 AASKDMRIRTVVANDDVASAPKAEIAKRRGVAGEIFMWKIGGAAAAQHYDLDGVIRVAQK 180

Query: 184 IAKAIGTLGVSLSPCSVPGT-KPTFELAADEMELGLGIHGEAGVRRIKLVPVDQIVTLML 242
                 ++G+ L+PC++    KP F++   +MELG+G HGE G+  I + P   +   ML
Sbjct: 181 TVDHCRSIGIGLTPCTIAAVGKPNFQIPDGQMELGIGHHGEPGIDVIPIEPAAAMAERML 240

Query: 243 DHMTDTSNISHVPVKSGSSVVLMVNNLGGLSFLELGIIADAAIRLLEGRGVKVARALVGT 302
             +    + S       +SVV++V+ LG    +EL I      + L  +G+K+ R  VG 
Sbjct: 241 APILADRDFS-----QDNSVVVLVSGLGATPVMELYIFYAEVEKQLTAKGLKIHRCYVGN 295

Query: 303 FMSALEMRGVSLTLMLVDEPLLKLID 328
           + ++LEM GV+LTL+ +D  L  LID
Sbjct: 296 YFTSLEMMGVTLTLLGLDAELTTLID 321


Lambda     K      H
   0.316    0.131    0.366 

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: 386
Number of extensions: 16
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: 578
Length of database: 333
Length adjustment: 32
Effective length of query: 546
Effective length of database: 301
Effective search space:   164346
Effective search space used:   164346
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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