GapMind for catabolism of small carbon sources

 

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

Align D-mannose and D-mannitol transporter (characterized)
to candidate PfGW456L13_3476 D-glucarate permease

Query= reanno::pseudo5_N2C3_1:AO356_28540
         (430 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3476
          Length = 467

 Score =  209 bits (532), Expect = 1e-58
 Identities = 134/420 (31%), Positives = 211/420 (50%), Gaps = 27/420 (6%)

Query: 6   RSLIIIMLFLAGVINYLDRSALSVAAPFIQKDYGLSTGEMGMIFSSFFVGYAAFNFIGGW 65
           R LI+ ++ +   ++  DR+ALSVA   + K+ G+S+ EMG +FS+F   Y  F    GW
Sbjct: 38  RFLILALITIVLALSTGDRAALSVAGTDMSKELGISSVEMGYLFSAFSWAYVIFLIPSGW 97

Query: 66  AADRYGAKTTLLLAMVLWSLFSGLTVLTVGFASLVL-----IRILFGMGEGPLSVTTSKM 120
             DR G+K +++LA+V+WS F+ +  + V F  +V+     +R L G  E P+   + ++
Sbjct: 98  LTDRIGSKLSMMLAVVIWSCFTVMMGM-VHFIGMVVPLLLALRFLLGAAESPVGPASGRI 156

Query: 121 VNNWYTPKRRARAIGASMSGTPLGGAISGPVVGFIAVTYGWKISFIIIMLIGLVWAAVWF 180
           +  W+    R  A     S   L  A+  PV+G++  TYGW+  FII+  IGLV  A+W+
Sbjct: 157 IAAWFPSSERGIAGAIFNSAQYLSLAVFTPVMGWLCYTYGWEYVFIIMGAIGLVIGAIWW 216

Query: 181 KFVK---ERPE-----------GEGAEDI--LRAEGQGELAAQPVFPLRFYLKQPTVLFT 224
           KF     + P+           G+G  D+  L+++         +  +    +   ++  
Sbjct: 217 KFYYLPIDHPKMNSEELEYIRAGDGLVDLESLKSKAANTGKGMKLGEIGQLFRSRMLVGI 276

Query: 225 SLAFFSYNYTLFFFLTWFPSYLTMAHGLNVKDMSIATVIPWVLGFLGLALGGFISDFVFK 284
            LA +      +FF+TWFP YL    G ++        IP + G +G    GFISD + K
Sbjct: 277 FLAQYCITSITWFFMTWFPIYLVKERGFDILQAGFIAAIPALCGLVGGVSSGFISDLILK 336

Query: 285 KTGRMMFSRKVVLVTCLLACAVCIACAGMVTTLYPAVILVALAVFFLYLTGAIYWAIIQD 344
           KTG +  +RK  +   LL  A  I C     +    V+L++LA FF    G++ W ++ D
Sbjct: 337 KTGSLSIARKTPITIGLLLSASIILC-NYAESAAVVVVLMSLA-FFGKGFGSMGWTVVAD 394

Query: 345 TVPAARVGGVSGFMHFLANTSGIVGPTLTGFLVQFTGSFTSAFLLAGLLTVIGAVCVARY 404
           T P   +G   G  +   NT+GIV P + G+++Q TGSF  A L  G     G V VA Y
Sbjct: 395 TAPKELIGTTGGVFNAFGNTAGIVTPVVIGYILQTTGSFDGALLYVG---AHGLVAVASY 451


Lambda     K      H
   0.329    0.142    0.439 

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: 622
Number of extensions: 37
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: 430
Length of database: 467
Length adjustment: 33
Effective length of query: 397
Effective length of database: 434
Effective search space:   172298
Effective search space used:   172298
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