GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Escherichia coli BW25113

Align Inositol transport system permease protein (characterized)
to candidate 17810 b3750 ribose ABC transporter permease protein (NCBI)

Query= reanno::WCS417:GFF2333
         (340 letters)



>FitnessBrowser__Keio:17810
          Length = 321

 Score =  213 bits (542), Expect = 5e-60
 Identities = 137/335 (40%), Positives = 194/335 (57%), Gaps = 34/335 (10%)

Query: 11  TVPTKSRRR------LPTELSIFLVLIGIGLVFELFGWIVRDQSFLMNSQRLVLMILQVS 64
           T  T S RR      L  + S+  +L+ I +V  L         F +N+  L  ++ Q S
Sbjct: 2   TTQTVSGRRYFTKAWLMEQKSLIALLVLIAIVSTL-----SPNFFTINN--LFNILQQTS 54

Query: 65  IIGLLAIGVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFSRAVFPSLTDLPVWIPVA 124
           +  ++A+G+T VI+T+GIDLS GS+LAL+  +AAS+               ++   + VA
Sbjct: 55  VNAIMAVGMTLVILTSGIDLSVGSLLALTGAVAASIVGI------------EVNALVAVA 102

Query: 125 MGLGVGLLAGAINGSIIAVTGIPPFIATLGMMVSARGLARYYTEGQPVSM----LSDSYT 180
             L +G   GA+ G I+A   +  FIATL MM+  RG+   YT G PV+      +D + 
Sbjct: 103 AALALGAAIGAVTGVIVAKGRVQAFIATLVMMLLLRGVTMVYTNGSPVNTGFTENADLFG 162

Query: 181 AIGHGA-----MPVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLII 235
             G G       PV I  +V +     L +T+ G+Y YA+GGN  A R SGINV +  II
Sbjct: 163 WFGIGRPLGVPTPVWIMGIVFLAAWYMLHHTRLGRYIYALGGNEAATRLSGINVNKIKII 222

Query: 236 VYSIAGLLAGLAGVVASARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGA 295
           VYS+ GLLA LAG++  AR ++ Q   G  YELDAIAA V+GGTSLAGG GRI GT+IGA
Sbjct: 223 VYSLCGLLASLAGIIEVARLSSAQPTAGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGA 282

Query: 296 LILGVMASGFTFVGVDAYIQDIIKGLIIVVAVVID 330
           LILG + +G   +GV +Y Q I+K ++I++AV++D
Sbjct: 283 LILGFLNNGLNLLGVSSYYQMIVKAVVILLAVLVD 317


Lambda     K      H
   0.325    0.140    0.394 

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: 270
Number of extensions: 11
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: 340
Length of database: 321
Length adjustment: 28
Effective length of query: 312
Effective length of database: 293
Effective search space:    91416
Effective search space used:    91416
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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