GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Phaeobacter inhibens BS107

Align Inositol transport system permease protein (characterized)
to candidate GFF2275 PGA1_c23070 putative ribose transport system permease protein

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



>FitnessBrowser__Phaeo:GFF2275
          Length = 333

 Score =  158 bits (400), Expect = 2e-43
 Identities = 106/324 (32%), Positives = 168/324 (51%), Gaps = 20/324 (6%)

Query: 26  IFLVLIGIGLVFELFGWIVRDQSFLMNSQRLVLMILQVSIIGLLAIGVTQVIITTGIDLS 85
           I L LI   +  E F   V D++F M++  ++L++ Q + IG++A+G+T V++   IDLS
Sbjct: 19  IVLELIFFSVAGEFFS--VSDKAF-MDTDNMLLLLKQSAPIGIIAMGMTIVMVNGNIDLS 75

Query: 86  SGSVLALSAMIAASLAQTSDFSRAVFPSLTDLPVWIPVAMGLGVGLLAGAINGSIIAVTG 145
            G++ A+ A+I          +  +F  L +  + +   + L  G++ GAING I+  TG
Sbjct: 76  VGAIYAICAIILLD-----SMTWTMFAGLGNWVIPVAWCLALLTGVVLGAINGLIVWKTG 130

Query: 146 IPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGHGAMPVI-------IFLVVAVI 198
           +  FI TLG M+  RGL   Y   QP S L+  +T +       +         LVV V 
Sbjct: 131 VDAFIVTLGSMLGYRGLVFMYNGEQPTSHLN--WTLVDFAEAQFLGLHTATWFLLVVTVA 188

Query: 199 FHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLIIVYSIAGLLAGLAGVVASARAATG 258
               +  T +G+  YAIG N +AA  +GI V  H++I + I G LA L+ VV  + + + 
Sbjct: 189 IWFLMNRTVHGRNAYAIGNNREAAVNAGIRVGPHMMINFMIIGFLAALSAVVFYSESGSV 248

Query: 259 QAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASGFTFVGVDAYIQDII 318
               G  YEL  I A V+GGT L GG G I  T  G + + ++  G   +G D    +++
Sbjct: 249 NPNDGQLYELWVITAVVLGGTKLTGGAGSIVSTFGGVIAIQLLRKGLAHIGADTSTVNLV 308

Query: 319 KGLIIVVAVVIDQYRN---KRKLK 339
            GLI++  + +D+  N   K +LK
Sbjct: 309 IGLILIAVLFLDRQLNVKGKEELK 332


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: 253
Number of extensions: 14
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: 340
Length of database: 333
Length adjustment: 28
Effective length of query: 312
Effective length of database: 305
Effective search space:    95160
Effective search space used:    95160
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