GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kgtP in Pseudomonas fluorescens FW300-N2C3

Align Alpha-ketoglutarate permease (characterized)
to candidate AO356_02260 AO356_02260 citrate-proton symporter

Query= SwissProt::P0AEX3
         (432 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_02260
          Length = 432

 Score =  218 bits (554), Expect = 4e-61
 Identities = 128/374 (34%), Positives = 207/374 (55%), Gaps = 16/374 (4%)

Query: 23  AIVGASSGNLVEWFDFYVYSFCSLYFAHIFFPSGNTTTQLLQTAGVFAAGFLMRPIGGWL 82
           AI    SGN +E FDF VY F +   A  FFP+ +    L+ +   F AGFLMRP+G   
Sbjct: 10  AIFRVVSGNFLEMFDFMVYGFYATAIAKTFFPADSAFVSLMLSLATFGAGFLMRPLGAIF 69

Query: 83  FGRIADKHGRKKSMLLSVCMMCFGSLVIACLPGYETIGTWAPALLLLARLFQGLSVGGEY 142
            G   D+HGR+K +++++ +M  G+++IAC+PGY  +G  AP L+LL RL QG S G E 
Sbjct: 70  LGAYIDRHGRRKGLIITLALMAMGTILIACVPGYAVLGVVAPLLVLLGRLLQGFSAGVEL 129

Query: 143 GTSATYMSEVAVEGRKGFYASFQYVTLIGGQLLALLVVVVLQHTMEDAALREWGWRIPFA 202
           G  + Y++E++  GRKGF+ S+Q  +     + A L+ V L H +    + +WGWR+PF 
Sbjct: 130 GGVSVYLAEISTPGRKGFFVSWQSASQQAAVVFAGLLGVGLNHWLSPQEMGDWGWRVPFL 189

Query: 203 LGAVLAVVALWLRRQLDETSQQETRALKEAGS--LKGLWRNRRAFIMVLGFTAAGSLCFY 260
           +G ++      +RR L+ET + + R  + + S  ++ + +N    +  +      ++ FY
Sbjct: 190 VGCMIVPAIFMIRRSLEETPEFQARKHRPSLSEIVRSIGQNFGIVLAGMALVVMTTVSFY 249

Query: 261 TFTTY---MQKYLVNTAGMHANVASGIMTAALFVFMLIQPLIGALSDKIGRRTSMLCFGS 317
             T Y     K  +N + + A + +  +  + F ++   P++GA SDKIGR+  +L    
Sbjct: 250 LITAYTPTFGKAELNLSDLDALLVTVCIGLSNFFWL---PVMGAFSDKIGRKPLLLGATI 306

Query: 318 LAAIFTVPILSALQNVSSPYAAFGLVMCALLIVSF-YTSISG---ILKAEMFPAQVRALG 373
           LA +   P LS L  V++P  +F  ++   L +SF Y S +G   +   E+ P +VR  G
Sbjct: 307 LAILTAYPALSWL--VANP--SFSHLLIVELWLSFLYGSYNGAMVVALTEIMPVEVRTTG 362

Query: 374 VGLSYAVANAIFGG 387
             L+Y++A A FGG
Sbjct: 363 FSLAYSLATATFGG 376


Lambda     K      H
   0.328    0.138    0.419 

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: 481
Number of extensions: 25
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: 432
Length of database: 432
Length adjustment: 32
Effective length of query: 400
Effective length of database: 400
Effective search space:   160000
Effective search space used:   160000
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 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