GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaM in Halomonas desiderata SP1

Align PEP-dependent dihydroxyacetone kinase, phosphoryl donor subunit DhaM; Dihydroxyacetone kinase subunit M; EC 2.7.1.121 (characterized)
to candidate WP_086509381.1 BZY95_RS07800 phosphoenolpyruvate--protein phosphotransferase

Query= SwissProt::D4GL26
         (473 letters)



>NCBI__GCF_002151265.1:WP_086509381.1
          Length = 963

 Score =  126 bits (317), Expect = 3e-33
 Identities = 111/360 (30%), Positives = 165/360 (45%), Gaps = 34/360 (9%)

Query: 139 PPAHAASLPAQAPDSDARSVTVTIR--NHHGLHVRPASRLVAALAGMNADL---VLEKQG 193
           P A AA++ A+     A + T   R  N HGLH RPA +LV A       +   + E  G
Sbjct: 262 PSADAATVLARLAGESAAAHTRLARVLNAHGLHARPAKQLVQAAREQGLPIQVRLAEGGG 321

Query: 194 QCVKPDSLNQIALLQVRCHDAVTLSASGPDAERALAAFESLAAEDFGEHP-------ESM 246
             V   SL ++  L  R    +  SA G  A++AL A     A+  GEH        E  
Sbjct: 322 AAVSASSLTKVINLGARRGQQLLFSAEGEGAQQALDAVCRAVADGLGEHVLPFDESRERS 381

Query: 247 ALKTSASTVEKVQ------------GKAVFYPLPLAQPA---RHPCSDVGQEERRLQQAI 291
             +  A+ VE +             G A+     L  P        +D  +++RRL+QA+
Sbjct: 382 MPQADAAPVEPLPDDVPHPGVAASPGLAIAPAFVLQTPRFDYPERAADPAEQQRRLRQAL 441

Query: 292 VDTLNDLNALAALAEKKYGASVAAIFSGHYTLLDDPDLFDAACKVIRNDSCCAESAWYQV 351
            +    L AL   A    G  VA I S H  +L DP+LF+AA + I+ +   AESAW++ 
Sbjct: 442 AEGAAQLEALVRQAR---GGEVAQILSMHEEMLTDPELFEAAREGIQ-EGRSAESAWWEA 497

Query: 352 LMELSQQYQHLDDAYLQARFIDIEDILYRSLCHLKGRDIRLPTP-DVPAIIVADDIFPSA 410
           +   +   + L D  L  R  D+ D+  R L  L   +++LP P + P I+V DDI PS 
Sbjct: 498 IETAAHAQEMLADRLLAERAADLRDVGRRVLGVLC--EVQLPEPPETPYILVTDDIGPSD 555

Query: 411 VVNLNAQLVKGICLREGSTLSHAAIIAQQAGIAFICQQGAVLDIIQPEDRLLIDPAAQRV 470
           V  L+ Q V+G+    G   +H+AI+A+  GI  +   G  +  +     L++D    RV
Sbjct: 556 VARLDTQRVRGLLTARGGATAHSAILARALGIPAVVGAGERVLTLAGGQELILDGERGRV 615


Lambda     K      H
   0.320    0.133    0.380 

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: 961
Number of extensions: 44
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: 473
Length of database: 963
Length adjustment: 39
Effective length of query: 434
Effective length of database: 924
Effective search space:   401016
Effective search space used:   401016
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: 54 (25.4 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