GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK in Sinorhizobium meliloti 1021

Align PTS-dependent dihydroxyacetone kinase 2, dihydroxyacetone-binding subunit DhaK; EC 2.7.1.121 (characterized)
to candidate SM_b20767 SM_b20767 dihydroxyacetone kinase

Query= SwissProt::Q92EU2
         (331 letters)



>FitnessBrowser__Smeli:SM_b20767
          Length = 572

 Score =  221 bits (563), Expect = 3e-62
 Identities = 125/316 (39%), Positives = 175/316 (55%), Gaps = 6/316 (1%)

Query: 16  LAGYVAAQGKYVDFAENDKRVIVSKQMSEEPRVRIIVGGGSGHEPLFLGYVGKDFADAAV 75
           LAG+ A   + V   +     +V      + +V ++VGGGSGH P F GYVG   ADAAV
Sbjct: 16  LAGFAAIYQRNVRLVKGG---VVRSTKVPKGKVAVVVGGGSGHYPAFAGYVGPGLADAAV 72

Query: 76  VGNINTSPSPEPCYNAVKAVDSGKGCLYMYGNYAGDVMNFDMGAEMAADDGIRVETVLVT 135
            G++  SPS        +  D G G L  +GNYAGDV+NF + AE    +GI V  + VT
Sbjct: 73  AGDVFASPSTAAVARVCRHADQGGGVLLGFGNYAGDVLNFGVAAERLRSEGIDVRILPVT 132

Query: 136 DDIYS--AENVEDRRGVAGDLIVFKAAASAAAKGLDLDAVKQAAEKANANTFSMGVALSS 193
           DD+ S  AE    RRG+AGDL+VFK A +AA  G  LD V++ A  AN  T S GVA   
Sbjct: 133 DDVASAPAETSAKRRGIAGDLVVFKIAGAAAEAGKSLDEVERLARHANDRTVSFGVAFGG 192

Query: 194 STLPVTGKAIFEMKEGEMEVGMGIHGEPGIKRTSIEPADKVVDQIMGYLIEEMKLTAGEE 253
            TLP     +F + +G+M +G+GIHGEPG+   +I  A  +   + G L+ E +     +
Sbjct: 193 CTLPGAAGPLFTVPKGQMALGLGIHGEPGVSEETIATASDLAKLLTGKLLAE-RPEGSRK 251

Query: 254 VHVLINGLGGLPVMDQYICYRRVDEILKEKGVHIHSPLVGNYATSMDMIGMSITLVRLDD 313
           V  ++NGLG     + ++ +  V   L + G+ I  P  G + TS+DM G S+TL+ LD+
Sbjct: 252 VAAVLNGLGSTKYEELFVLWTAVARQLNDAGLEIVDPECGEFVTSLDMQGCSLTLLWLDE 311

Query: 314 ELKDLLDTPCDTPYFK 329
           EL+ L   P D P  +
Sbjct: 312 ELEALWRAPTDAPVLR 327


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: 440
Number of extensions: 22
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: 572
Length adjustment: 32
Effective length of query: 299
Effective length of database: 540
Effective search space:   161460
Effective search space used:   161460
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