GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Pseudomonas simiae WCS417

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate GFF3462 PS417_17725 ribose ABC transporter permease

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__WCS417:GFF3462
          Length = 330

 Score =  179 bits (454), Expect = 9e-50
 Identities = 109/315 (34%), Positives = 178/315 (56%), Gaps = 12/315 (3%)

Query: 14  RRFRWPTGMPQLVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPV-ALLAIG 72
           R  R P   P  V L++V LV          ++  D  L  S +  + R   + A++A+G
Sbjct: 25  RLVRSPAFYP-FVGLVVVTLV---------MILASDTFLTASNLSNIARQVSINAIIAVG 74

Query: 73  MTLVIATGGIDLSVGAVMAIAGATTAAMTVAGFSLPIVLLSALGTGILAGLWNGILVAIL 132
           MT VI TGGIDLSVG VMA++G  TA + VAG    + + + +  G+  G+ NG+ VA L
Sbjct: 75  MTCVILTGGIDLSVGPVMALSGTLTAGLMVAGLPPGLAIGAGMLIGVAFGIGNGLFVAYL 134

Query: 133 KIQPFVATLILMVAGRGVAQLITAGQIVTFNSPDLSWFGSGSLLFLPTPVIIAVLTLILF 192
            + P + TL  M   RG+  + T G  ++      ++FG  SL  +  P++I +LT ++ 
Sbjct: 135 HMPPIIVTLATMGIARGLGLMYTDGYPISGLPDWFAFFGRESLFGIQVPILIMLLTYLVA 194

Query: 193 WLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVAADIRGAD 252
           ++L + T +G +I A+G N  A + +GV      +L Y +SGL AAIAG+++ + +    
Sbjct: 195 YVLLQHTRIGRYIYAIGGNEEAVRLSGVRAARFKLLVYGISGLTAAIAGLVLTSRLMSGQ 254

Query: 253 ANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFPPEMNQVV 312
             NAG+  ELDAI AVV+GG S+ GGR  ++ +++GA+++  +N G+ + G  P +  V+
Sbjct: 255 P-NAGVSFELDAIAAVVLGGASIAGGRGVIVGTLLGAMLLGVLNNGLNMLGVSPYVQSVI 313

Query: 313 KAVVVLCVLIVQSQR 327
           K  ++L  + +  QR
Sbjct: 314 KGGIILLAIFISRQR 328


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: 313
Number of extensions: 15
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: 330
Length adjustment: 28
Effective length of query: 313
Effective length of database: 302
Effective search space:    94526
Effective search space used:    94526
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