GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolC in Burkholderia phytofirmans PsJN

Align 5-dehydro-2-deoxygluconokinase 1; EC 2.7.1.92; 2-deoxy-5-keto-D-gluconate kinase 1; DKG kinase 1 (uncharacterized)
to candidate BPHYT_RS11300 BPHYT_RS11300 2-dehydro-3-deoxygluconokinase

Query= curated2:Q63B75
         (332 letters)



>FitnessBrowser__BFirm:BPHYT_RS11300
          Length = 327

 Score =  118 bits (295), Expect = 2e-31
 Identities = 93/324 (28%), Positives = 149/324 (45%), Gaps = 8/324 (2%)

Query: 7   KENRPFDLIAVGRLCVDLNANETQRPMEETRTFTKYVGGSPANIAIGAARLGLQTGFIGK 66
           K     D+I  G       A ET  P+     FTK V G+  N+AIG +RLG + G++ +
Sbjct: 3   KTTTSLDVITYGEAMAMFVAAETG-PLAGVGQFTKRVAGADLNVAIGLSRLGFKVGWMSR 61

Query: 67  VSDDQMGRFITGYLKDNKINTDQIRIDCTGAVTGLAFTEIKSPEDCSILMYRDNVADLNL 126
           V +D  G+++   L    I+   +  D          ++     D +I  +R   A  +L
Sbjct: 62  VGNDSFGQYVRDTLTKEGIDQGCVTTDERYPTGFQLKSKNDDGSDPAIEYFRKGSAASHL 121

Query: 127 DPTEVSEDYIKQSKALLISGTALAKSPS-REAVFLALEYARKHDVVVFFDVDYRPYTWQS 185
              + + DY+ Q++ L ++G A A S S RE  F      R     + FD + RP  W S
Sbjct: 122 SLADYAADYVLQARHLHLTGVAPAISASSRELAFHLAREMRAAGKTISFDPNLRPTLWPS 181

Query: 186 EAETAVYYNLAAEKSDVIIGTREEFDMMEKLLNYEQSNDQVTAERWFSHYAKIVVIKHGG 245
            A      N  A  +D ++    E ++   L  Y Q +D   A+ +    A+ V+IK G 
Sbjct: 182 RAAMVEGLNALAALADWVLPGIGEGEI---LTGYTQPDD--IAKFYLEQGARGVIIKLGA 236

Query: 246 DGSIAYTRDGQSHRGGIFKTKVLKTFGAGDSYASAFIYGLIQGLEIPQAMRLGGASASIV 305
            G+   T D  +   G    KV+ T GAGD +A   +  L++G  +PQA+  G    ++ 
Sbjct: 237 QGAYFRTADDAAMIAGQPVAKVVDTVGAGDGFAVGVVSALLEGKSLPQAVARGNRIGALA 296

Query: 306 ISKHSCSDAMPTRAEISAFMETAE 329
           I     S+ +P+RAE+ A +E A+
Sbjct: 297 IQVIGDSEGLPSRAELDA-LEAAQ 319


Lambda     K      H
   0.318    0.134    0.385 

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: 206
Number of extensions: 12
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: 332
Length of database: 327
Length adjustment: 28
Effective length of query: 304
Effective length of database: 299
Effective search space:    90896
Effective search space used:    90896
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 (21.7 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