GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Klebsiella michiganensis M5al

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate BWI76_RS00280 BWI76_RS00280 ribose ABC transporter permease

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__Koxy:BWI76_RS00280
          Length = 321

 Score =  193 bits (490), Expect = 6e-54
 Identities = 115/314 (36%), Positives = 184/314 (58%), Gaps = 13/314 (4%)

Query: 18  WPTGMPQLVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPVALLAIGMTLVI 77
           W      L+ALL+++ + S ++P+F+ V      LF    +IL + +  A++A+GMTLVI
Sbjct: 16  WLMEQKSLIALLVLIAIVSTMSPNFFTV----NNLF----NILQQTSVNAIMAVGMTLVI 67

Query: 78  ATGGIDLSVGAVMAIAGATTAAMTVAGFSLPIVLLSALGTGILAGLWNGILVAILKIQPF 137
            T GIDLSVG+++A+ GA  A++     +  + + +AL  G   G   G++VA  ++Q F
Sbjct: 68  LTSGIDLSVGSLLALTGAVAASIVGIEVNALVAVAAALALGAAIGAVTGVIVAKGRVQAF 127

Query: 138 VATLILMVAGRGVAQLITAGQIV----TFNSPDLSWFGSGSLLFLPTPVIIAVLTLILFW 193
           +ATL++M+  RGV  + T G  V    T N+    WFG G  L +PTPV I  +  +  W
Sbjct: 128 IATLVMMLLLRGVTMVYTNGSPVNTGFTDNADLFGWFGIGRPLGIPTPVWIMAIVFLAAW 187

Query: 194 LLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVAADIRGADA 253
            +   T LG +I A+G N  A + +G++   + ++ Y L G+ A++AGII  A +  A  
Sbjct: 188 YMLHHTRLGRYIYALGGNEAATRLSGISVNKVKIIVYSLCGMLASLAGIIEVARLSSAQP 247

Query: 254 NNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFPPEMNQVVK 313
             AG   ELDAI AVV+GG SL GG+  ++ +++GALI+  +N G+ L G       +VK
Sbjct: 248 -TAGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQMIVK 306

Query: 314 AVVVLCVLIVQSQR 327
           AVV+L  ++V +++
Sbjct: 307 AVVILLAVLVDNKK 320


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: 297
Number of extensions: 16
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: 321
Length adjustment: 28
Effective length of query: 313
Effective length of database: 293
Effective search space:    91709
Effective search space used:    91709
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