GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Paraburkholderia bryophila 376MFSha3.1

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate H281DRAFT_02175 H281DRAFT_02175 monosaccharide ABC transporter membrane protein, CUT2 family

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__Burk376:H281DRAFT_02175
          Length = 353

 Score =  197 bits (500), Expect = 4e-55
 Identities = 117/319 (36%), Positives = 180/319 (56%), Gaps = 15/319 (4%)

Query: 11  TPKRRFRWPTGMPQLVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPVALLA 70
           T  R +R      +++ LL ++L + +  PHFW +   +  L         +   + ++ 
Sbjct: 41  TGVRNWRRLAMQREVIVLLAMVLFNLIFTPHFWSLQTFNVNL--------TQVVTIVIVG 92

Query: 71  IGMTLVIATGGIDLSVGAVMAIAGATTAAMTV-----AGFSLPIVLLSALGTGILAGLWN 125
           IGMTLV+ATGGIDLSVGA MAI+GA    + +      G +L  VL   +    L G++N
Sbjct: 93  IGMTLVVATGGIDLSVGASMAISGALAPMLFLNIPVPGGIALAFVL--PVLAAALCGVFN 150

Query: 126 GILVAILKIQPFVATLILMVAGRGVAQLITAGQIVTFNSPDLSWFGSGSLLFLPTPVIIA 185
           G+LV  L +QP VATL+L +AGRG+AQ++T G +  FN+P   W   G +  +P  V++ 
Sbjct: 151 GLLVTRLAVQPIVATLVLFIAGRGIAQVVTDGSLQAFNTPAFQWIALGKVAGVPFQVLLM 210

Query: 186 VLTLILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVA 245
           +  ++ F  + RKT  G ++   G N +AA  +GV T  + ++ Y L    A +AG+I  
Sbjct: 211 LALVVAFAWVVRKTLFGQYLLITGGNEKAAYLSGVPTASVKLIAYTLCAALAGLAGLISI 270

Query: 246 ADIRGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFP 305
           +    +DAN  GL +ELDAI AV +GG +L GG+  +  ++VGALIIQ +   +L  G P
Sbjct: 271 SVNSSSDANVVGLGIELDAIAAVAVGGTALTGGKAFIGGTLVGALIIQLLRYTLLAHGIP 330

Query: 306 PEMNQVVKAVVVLCVLIVQ 324
                VVKA +++  + VQ
Sbjct: 331 DAAALVVKAGIIVAAVYVQ 349


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: 325
Number of extensions: 12
Number of successful extensions: 3
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: 353
Length adjustment: 29
Effective length of query: 312
Effective length of database: 324
Effective search space:   101088
Effective search space used:   101088
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:

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