GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Psest_0085 in Phaeobacter inhibens BS107

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate GFF1596 PGA1_c16180 TRAP transporter solute receptor, TAXI family

Query= reanno::psRCH2:GFF85
         (317 letters)



>FitnessBrowser__Phaeo:GFF1596
          Length = 321

 Score =  171 bits (432), Expect = 3e-47
 Identities = 110/320 (34%), Positives = 157/320 (49%), Gaps = 8/320 (2%)

Query: 1   MRLTKRLGLLAAAAAFTASTAAVAAPTFINILTGGTSGVYYPIGVALSQQYNKI---DGA 57
           M  TK       A AF A  A   A  FI I TGG +GVYYP G A+ +  NK     G 
Sbjct: 1   MTNTKLAVSALVATAFMAPAAM--AEEFITIGTGGVTGVYYPTGGAICRLVNKTRKEHGI 58

Query: 58  KTSVQATKASVENLNLLQAGRGELAFSLGDSVEDAWNGVEDAGFKAPLKRLRAIAGTYNN 117
           + SV++T  SV N+N ++ G  E   +  D    A+NG      +   + LRA+   +  
Sbjct: 59  RCSVESTGGSVYNINTIREGELEFGVAQSDWQYHAYNGTSKFEEQGAFEGLRAVFSVHPE 118

Query: 118 YIQIVASAESGIKTLDDLKGKRISVGAPKSGTELNARAIFKAAGLDYKDMGRVEFLPYAE 177
              +VA A++G+ + DDLKGKR+++G P SG       + +A G           L  AE
Sbjct: 119 PFTVVARADAGVTSFDDLKGKRVNIGNPGSGQRGTMEVLLEAKGWGMDAFALATELKAAE 178

Query: 178 SVELIKNRQLDATLQSSGLGMAAIRDLASTMPVTFVEIPAEVVEKIESD--AYLAGVIPA 235
               + + Q+DA + + G    +I++  +      V +  E VEK+ +D   Y    IP 
Sbjct: 179 QSAALCDNQIDAMVYTVGHPSGSIQEATTACDSVLVTVDGEAVEKLIADNSFYRTATIPG 238

Query: 236 GTYDGQDADVPTVAITNILVTHEKVSDEVAYQMTKLMFDNLAALGNAHSAAKDIKLEN-A 294
           G Y G DADV T  +    VT ++VSDE  Y + K +F+N       H A  ++K E  A
Sbjct: 239 GMYRGSDADVGTFGVGATFVTSDQVSDEAVYTVVKAVFENFDDFKKLHPAFANLKPEEMA 298

Query: 295 TKNLPIPLHPGAERFYKEAG 314
           T  L  PLHPGA ++YKE G
Sbjct: 299 TAGLSAPLHPGAAKYYKEQG 318


Lambda     K      H
   0.314    0.131    0.359 

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: 225
Number of extensions: 8
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: 317
Length of database: 321
Length adjustment: 28
Effective length of query: 289
Effective length of database: 293
Effective search space:    84677
Effective search space used:    84677
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: 42 (22.0 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