GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Burkholderia phytofirmans PsJN

Align fructokinase (EC 2.7.1.4) (characterized)
to candidate BPHYT_RS09175 BPHYT_RS09175 2-dehydro-3-deoxygluconokinase

Query= BRENDA::Q42645
         (331 letters)



>FitnessBrowser__BFirm:BPHYT_RS09175
          Length = 312

 Score =  132 bits (332), Expect = 1e-35
 Identities = 99/316 (31%), Positives = 154/316 (48%), Gaps = 20/316 (6%)

Query: 14  VVSFGEMLIDFVPTSSGVSLAEAPGFLKAPGGAPANVAIAVSRLGGNAAFVGKLGDDEFG 73
           +++ GE +I+F       S  + P +L+  GG  +N  IA +R G    FV  +G D FG
Sbjct: 12  ILALGEAMIEF-----NQSAKDQPNYLQGFGGDTSNFCIAAARQGAQTGFVSAVGADHFG 66

Query: 74  HMLAGILKKNGVSADGLSFDKGARTALAFVTLKSDGEREFMFYRNPSADMLLTPDELNLD 133
            +L  + ++  V    +  D  A T + FV+   +G   F + R  SA     P +L LD
Sbjct: 67  RLLVDLWEREQVDTSLVRVDPQASTGVYFVSHGPNG-HAFDYLRAGSAASRYAPHDLPLD 125

Query: 134 LIRSAKVFHYGSIRLIVE-PCRSAHLKAMEEAKKAGALLSYDPNLRLPLWPSAEEAREQI 192
            I +AKV H   I L +      A L+A+  A+  G  +S+D NLRL LWP A  AR  +
Sbjct: 126 AIAAAKVIHLSGISLAISLSACDAALEAIAHARANGVRVSFDTNLRLKLWPLA-RARAVM 184

Query: 193 MSIWDKAEVIKVSDNELEFLTGNSTIDDATAMSLWHPNLKLLLVTLGDQGCRYYTKNFKG 252
           +    + ++   S +++  LTG +  D+     L H    ++ + LG +G    T N + 
Sbjct: 185 LEAIRQTDICLPSWDDVTDLTGLTGRDEIVDFLLSH-GPSVVALKLGKEGSYIATPNERR 243

Query: 253 SLDGFKVNAVDTTGAGDSFVGALLNKIV--DDHSIIEDESRLKEVLKFANACGAITTTKK 310
            + G  VNAVD TGAGD F GA + +IV  DD              ++AN   A++T   
Sbjct: 244 VVPGHVVNAVDATGAGDCFGGAFIARIVAGDDPF---------TAARYANVAAALSTQGY 294

Query: 311 GAIPALPTVADALELI 326
           GA+  +P+ A   +L+
Sbjct: 295 GAVAPIPSRATVEQLL 310


Lambda     K      H
   0.316    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: 245
Number of extensions: 15
Number of successful extensions: 4
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: 312
Length adjustment: 28
Effective length of query: 303
Effective length of database: 284
Effective search space:    86052
Effective search space used:    86052
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: 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