GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK in Brucella inopinata BO1

Align PTS-dependent dihydroxyacetone kinase 2, dihydroxyacetone-binding subunit DhaK; EC 2.7.1.121 (characterized)
to candidate WP_002969174.1 BIBO1_RS11570 dihydroxyacetone kinase subunit DhaK

Query= SwissProt::Q92EU2
         (331 letters)



>NCBI__GCF_000182725.1:WP_002969174.1
          Length = 330

 Score =  259 bits (662), Expect = 6e-74
 Identities = 133/322 (41%), Positives = 201/322 (62%), Gaps = 3/322 (0%)

Query: 1   MRRLVNDGYEAVEEMLAGYVAAQGKYVDFAENDKRVIVSKQMSEEPRVRIIVGGGSGHEP 60
           M+R +N+  E VE+ + G+V A    +  AEN  RVI +K      +V ++ GGGSGHEP
Sbjct: 1   MQRFINNPDEVVEDTVRGFVKAHSDIIRLAENP-RVIAAKDAPVAGKVGVVTGGGSGHEP 59

Query: 61  LFLGYVGKDFADAAVVGNINTSPSPEPCYNAVKAVDSGKGCLYMYGNYAGDVMNFDMGAE 120
            F+GY GK+  DA  VG + +SP+ +  ++A++  + GKG + +YGNYAGD MN  M  +
Sbjct: 60  AFIGYTGKNMLDAVAVGELFSSPTAKSFHDAIREANGGKGVVVLYGNYAGDNMNVKMATK 119

Query: 121 MAADDGIRVETVLVTDDIYSAENVE--DRRGVAGDLIVFKAAASAAAKGLDLDAVKQAAE 178
           +AA DGI V TV+  DD+ SA   E   RRGVAG++ ++K   + AA G  L+ V+  A+
Sbjct: 120 LAAKDGIDVATVVANDDVCSAPAAEREKRRGVAGEIFMWKVGGAKAATGATLEEVRATAQ 179

Query: 179 KANANTFSMGVALSSSTLPVTGKAIFEMKEGEMEVGMGIHGEPGIKRTSIEPADKVVDQI 238
           KA  N  S+GV L   TLP  G   FE+  G MEVG+G HGEPG++   ++ A +V   +
Sbjct: 180 KAIDNCRSIGVGLGPCTLPAVGHPNFEIAPGTMEVGIGHHGEPGVRVEPLKSAAEVARDM 239

Query: 239 MGYLIEEMKLTAGEEVHVLINGLGGLPVMDQYICYRRVDEILKEKGVHIHSPLVGNYATS 298
              ++++  L  G EV VL++GLG  P+ + YI    ++  ++ +G+ IH   +GNY TS
Sbjct: 240 CQIVLDDHGLAEGTEVAVLVSGLGATPLNELYILNDTIETEIRARGLKIHRTYIGNYFTS 299

Query: 299 MDMIGMSITLVRLDDELKDLLD 320
           ++M+G ++T++ LD ELK+LLD
Sbjct: 300 LEMVGATLTVMALDSELKELLD 321


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: 293
Number of extensions: 14
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: 330
Length adjustment: 28
Effective length of query: 303
Effective length of database: 302
Effective search space:    91506
Effective search space used:    91506
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 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