GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK in Pseudomonas simiae WCS417

Align PTS-dependent dihydroxyacetone kinase 2, dihydroxyacetone-binding subunit DhaK; EC 2.7.1.121 (characterized)
to candidate GFF2361 PS417_12040 dihydroxyacetone kinase

Query= SwissProt::Q92EU2
         (331 letters)



>FitnessBrowser__WCS417:GFF2361
          Length = 333

 Score =  264 bits (675), Expect = 2e-75
 Identities = 139/325 (42%), Positives = 204/325 (62%), Gaps = 3/325 (0%)

Query: 1   MRRLVNDGYEAVEEMLAGYVAAQGKYVDFAENDKRVIVSKQMSEEPRVRIIVGGGSGHEP 60
           M R++ND  + VE+ML G + A  +   + E + RVIV  + S   RV I+ GGGSGHEP
Sbjct: 1   MNRVINDPDQVVEDMLRGILVAHPELRQY-ETNPRVIVKAKPSGPGRVGIVTGGGSGHEP 59

Query: 61  LFLGYVGKDFADAAVVGNINTSPSPEPCYNAVKAVDSGKGCLYMYGNYAGDVMNFDMGAE 120
            FLGYVG    DA  VG I +SP+ +  ++A +A D G G   +YGNYAGD MN  +  +
Sbjct: 60  AFLGYVGPGLVDAVAVGEIFSSPTAKSFFDAFRAADHGAGVACLYGNYAGDNMNVKLAMK 119

Query: 121 MAADDGIRVETVLVTDDIYSAENVE--DRRGVAGDLIVFKAAASAAAKGLDLDAVKQAAE 178
           MAA   +R+ TV+  DD+ SA   E   RRGVAG++ ++K   +AAA+  DLD V + A+
Sbjct: 120 MAASKDMRIRTVVANDDVASAPKAEIAKRRGVAGEIFMWKIGGAAAAQHYDLDGVIRVAQ 179

Query: 179 KANANTFSMGVALSSSTLPVTGKAIFEMKEGEMEVGMGIHGEPGIKRTSIEPADKVVDQI 238
           K   +  S+G+ L+  T+   GK  F++ +G+ME+G+G HGEPGI    IEPA  + +++
Sbjct: 180 KTVDHCRSIGIGLTPCTIAAVGKPNFQIPDGQMELGIGHHGEPGIDVIPIEPAAAMAERM 239

Query: 239 MGYLIEEMKLTAGEEVHVLINGLGGLPVMDQYICYRRVDEILKEKGVHIHSPLVGNYATS 298
           +  ++ +   +    V VL++GLG  PVM+ YI Y  V++ L  KG+ IH   VGNY TS
Sbjct: 240 LAPILADRDFSQDNSVVVLVSGLGATPVMELYIFYAEVEKQLTAKGLKIHRCYVGNYFTS 299

Query: 299 MDMIGMSITLVRLDDELKDLLDTPC 323
           ++M+G+++TL+ LD EL  L+D PC
Sbjct: 300 LEMMGVTLTLLGLDAELTTLIDQPC 324


Lambda     K      H
   0.317    0.136    0.386 

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: 284
Number of extensions: 11
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: 331
Length of database: 333
Length adjustment: 28
Effective length of query: 303
Effective length of database: 305
Effective search space:    92415
Effective search space used:    92415
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: 49 (23.5 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