GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Shewanella sp. ANA-3

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate 7024901 Shewana3_2075 inner-membrane translocator (RefSeq)

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__ANA3:7024901
          Length = 405

 Score =  335 bits (858), Expect = 2e-96
 Identities = 184/320 (57%), Positives = 234/320 (73%), Gaps = 6/320 (1%)

Query: 10  TTPKRRFRWPTGMPQLVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPVALL 69
           +T   R+ WP     L+AL ++LL +  +   F+ +  QD RL+GS IDILNR+APVALL
Sbjct: 56  STSMGRYLWP-----LLALSILLLANLFIDSSFFNISYQDDRLYGSLIDILNRSAPVALL 110

Query: 70  AIGMTLVIATGGIDLSVGAVMAIAGATTA-AMTVAGFSLPIVLLSALGTGILAGLWNGIL 128
           +IGM+LVIATGGIDLSVGAVMAIAGA  A  + V   SL  V+ + L  G+LAG  NG L
Sbjct: 111 SIGMSLVIATGGIDLSVGAVMAIAGAVCANLLLVPDISLVTVIAAGLIVGLLAGCINGGL 170

Query: 129 VAILKIQPFVATLILMVAGRGVAQLITAGQIVTFNSPDLSWFGSGSLLFLPTPVIIAVLT 188
           V+ L IQP VATL+LMVAGRGVAQLI  GQI+TF  P  +  G G  L LP PV I +  
Sbjct: 171 VSFLGIQPIVATLLLMVAGRGVAQLINQGQIITFQHPGFAAIGVGQFLGLPMPVWIVIGM 230

Query: 189 LILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVAADI 248
           L    LL RKTALG+FIEAVG N +A++  G+N + I +  Y ++GLCAA+AG+I  ADI
Sbjct: 231 LTFSQLLLRKTALGLFIEAVGCNAKASRYLGINDKSIKLFAYGIAGLCAALAGMISTADI 290

Query: 249 RGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFPPEM 308
           +G+DANNAGLWLELDA+LAVVIGG +L GGRF+L+LSVVGALIIQ + T I++SG P + 
Sbjct: 291 QGSDANNAGLWLELDAVLAVVIGGAALTGGRFSLILSVVGALIIQTLATTIIVSGLPAKF 350

Query: 309 NQVVKAVVVLCVLIVQSQRF 328
           N ++KA+V+L VL++QS +F
Sbjct: 351 NLLIKAIVILTVLLLQSAKF 370


Lambda     K      H
   0.327    0.142    0.416 

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: 367
Number of extensions: 13
Number of successful extensions: 2
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: 341
Length of database: 405
Length adjustment: 30
Effective length of query: 311
Effective length of database: 375
Effective search space:   116625
Effective search space used:   116625
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 (21.7 bits)
S2: 49 (23.5 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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