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_b20312 SM_b20312 dihydroxyacetone kinase

Query= SwissProt::Q92EU2
         (331 letters)



>FitnessBrowser__Smeli:SM_b20312
          Length = 695

 Score =  315 bits (808), Expect = 2e-90
 Identities = 157/333 (47%), Positives = 219/333 (65%), Gaps = 2/333 (0%)

Query: 1   MRRLVNDGYEAVEEMLAGYVAAQGKYVDFAENDKRVIVSKQMSEEPRVRIIVGGGSGHEP 60
           +++ +N+  E VEEML G V A   Y+       R +V++      +V +++GGG+GHEP
Sbjct: 363 VKKFLNNPNEVVEEMLDGAVKAHEIYLQPINGSHRALVARNGPRPGKVGLVIGGGTGHEP 422

Query: 61  LFLGYVGKDFADAAVVGNINTSPSPEPCYNAVKAVDSGKGCLYMYGNYAGDVMNFDMGAE 120
            FLGYVGK  ADA  VGNI +SP P+P     +A   G+G L++YGNYAGDVMNF+M AE
Sbjct: 423 CFLGYVGKGLADAVAVGNIFSSPPPDPIVQCAEAASGGEGVLFVYGNYAGDVMNFEMAAE 482

Query: 121 MAADDGIRVETVLVTDDIYSA--ENVEDRRGVAGDLIVFKAAASAAAKGLDLDAVKQAAE 178
           +A + GI+V+TVL TDD+ S+  E+ E RRGVAG+  +FK A +A  +GL L+A +    
Sbjct: 483 IAEEKGIKVKTVLTTDDVASSPVEDREGRRGVAGNFFIFKIAGAACDRGLSLEACEAVTR 542

Query: 179 KANANTFSMGVALSSSTLPVTGKAIFEMKEGEMEVGMGIHGEPGIKRTSIEPADKVVDQI 238
           KAN  T+++GVAL   ++P T +  FE+   +MEVGMGIHGEPG+ R  I  AD++ D I
Sbjct: 543 KANLRTYTVGVALEPGSMPQTRRHNFEIGPDDMEVGMGIHGEPGVTRERIRSADEITDSI 602

Query: 239 MGYLIEEMKLTAGEEVHVLINGLGGLPVMDQYICYRRVDEILKEKGVHIHSPLVGNYATS 298
           M  + +EMK   GE V VL+N  G  P+M+ YI +RRV + L  K + I +  +G+Y TS
Sbjct: 603 MDRIFKEMKTAPGERVAVLVNSFGATPLMELYILFRRVQQRLAAKDILIEANWIGHYCTS 662

Query: 299 MDMIGMSITLVRLDDELKDLLDTPCDTPYFKVD 331
           +DM G SIT++ LD EL DLL  PC+T + KV+
Sbjct: 663 LDMAGASITILHLDQELSDLLHHPCETAFLKVN 695


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: 525
Number of extensions: 28
Number of successful extensions: 2
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: 695
Length adjustment: 33
Effective length of query: 298
Effective length of database: 662
Effective search space:   197276
Effective search space used:   197276
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