GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguK in Pseudomonas fluorescens GW456-L13

Align 2-ketogluconokinase (EC 2.7.1.13) (characterized)
to candidate PfGW456L13_2950 2-ketogluconate kinase (EC 2.7.1.13)

Query= metacyc::MONOMER-12748
         (320 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2950
          Length = 328

 Score =  475 bits (1223), Expect = e-139
 Identities = 241/307 (78%), Positives = 259/307 (84%)

Query: 1   MPDIDILSFGETMAMFVAEHGGDLAQVQHFHKRIAGADSNVAIGLARLGFKVAWLSRVGN 60
           M +IDILSFGETMAMFVAE  GDLA V  FHKRIAGADSNVAIGL+RLGF VAWLSRVG 
Sbjct: 1   MSEIDILSFGETMAMFVAEQTGDLASVNEFHKRIAGADSNVAIGLSRLGFNVAWLSRVGA 60

Query: 61  DSLGRFVLDTLRAEGLDCRFVRCDPIHPTGFQLKSREDGGDDPRVEYFRRGSAASHLAIS 120
           DSLGRFV+DTL  EGLDCR V  DP HPTGFQLKSR D G DP VEYFRRGSAASHL+  
Sbjct: 61  DSLGRFVIDTLEKEGLDCRHVDIDPAHPTGFQLKSRTDDGSDPVVEYFRRGSAASHLSSH 120

Query: 121 DLDPALLRARHLHATGIPPALSDSARELSGHLMHTQRSAGHSVSFDPNLRPALWPSEALM 180
            + P LL+ARHLHATGIP ALS++AR++S  LM   R AG SVSFDPNLRP+LW SE LM
Sbjct: 121 SIVPDLLKARHLHATGIPAALSETARQMSFELMTRMRDAGRSVSFDPNLRPSLWASERLM 180

Query: 181 IREINRLAALAHWVLPGLAEGRLLTGRDDPADIAAFYLDQGAEAVVIKLGAHGAYYRTQL 240
           I EINRLAALAHWVLPGL+EGRLLTG +DPADIAAFYLDQGAEAV IKLG HGAYYRT L
Sbjct: 181 ITEINRLAALAHWVLPGLSEGRLLTGFEDPADIAAFYLDQGAEAVAIKLGPHGAYYRTHL 240

Query: 241 DAGFVEGVPVAQVVDTVGAGDGFAVGLISALLESRGILEAVQRANWIGSRAVQSRGDMEG 300
           D GFV GVPV  VVDTVGAGDGFAVG+ISALLE+    +AV+RANWIGSRAVQSRGDMEG
Sbjct: 241 DQGFVAGVPVQTVVDTVGAGDGFAVGMISALLENHSFADAVRRANWIGSRAVQSRGDMEG 300

Query: 301 LPLRHEL 307
           LP R E+
Sbjct: 301 LPTRSEM 307


Lambda     K      H
   0.321    0.138    0.414 

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: 438
Number of extensions: 14
Number of successful extensions: 1
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: 320
Length of database: 328
Length adjustment: 28
Effective length of query: 292
Effective length of database: 300
Effective search space:    87600
Effective search space used:    87600
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 (21.9 bits)
S2: 48 (23.1 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