GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Pseudomonas simiae WCS417

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate GFF3462 PS417_17725 ribose ABC transporter permease

Query= uniprot:D8J112
         (347 letters)



>FitnessBrowser__WCS417:GFF3462
          Length = 330

 Score =  217 bits (553), Expect = 3e-61
 Identities = 126/332 (37%), Positives = 192/332 (57%), Gaps = 11/332 (3%)

Query: 14  TMANTASAQGLRARLFNPAARQKLLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVN 73
           T  +T  +  LR  L           F  L+++ L    AS  F+   NL +I +  ++N
Sbjct: 9   TSISTGDSSRLRLNLARLVRSPAFYPFVGLVVVTLVMILASDTFLTASNLSNIARQVSIN 68

Query: 74  GVLAIACTYVIITSGIDLSVGTMMTFCAVM-AGVVLTNWGMPLPLGIAAAIFFGALSGWI 132
            ++A+  T VI+T GIDLSVG +M     + AG+++   G+P  L I A +  G   G  
Sbjct: 69  AIIAVGMTCVILTGGIDLSVGPVMALSGTLTAGLMVA--GLPPGLAIGAGMLIGVAFGIG 126

Query: 133 SGMVIAKLKVPPFIATLGMMMLLKGLSLVISGTRPIYFNDTEGFSAIAQDSLIGDLIPSL 192
           +G+ +A L +PP I TL  M + +GL L+ +   PI     + F+   ++SL G  +P  
Sbjct: 127 NGLFVAYLHMPPIIVTLATMGIARGLGLMYTDGYPIS-GLPDWFAFFGRESLFGIQVP-- 183

Query: 193 PIPNAVLILFLVAIGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAI 252
                +LI+ L  + A ++L  T  GRY +A+G NEEA+RLSGV+   +K+ VY  SG  
Sbjct: 184 -----ILIMLLTYLVAYVLLQHTRIGRYIYAIGGNEEAVRLSGVRAARFKLLVYGISGLT 238

Query: 253 CGIAGLIIASRLNSAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVN 312
             IAGL++ SRL S QP  G  +ELDAIAAVV+GG S++GG G I+GT++GA ++ VL N
Sbjct: 239 AAIAGLVLTSRLMSGQPNAGVSFELDAIAAVVLGGASIAGGRGVIVGTLLGAMLLGVLNN 298

Query: 313 GLRIMSVAQEWQTVVTGVIIILAVYLDILRRR 344
           GL ++ V+   Q+V+ G II+LA+++   R +
Sbjct: 299 GLNMLGVSPYVQSVIKGGIILLAIFISRQRHK 330


Lambda     K      H
   0.326    0.139    0.398 

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: 273
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: 347
Length of database: 330
Length adjustment: 28
Effective length of query: 319
Effective length of database: 302
Effective search space:    96338
Effective search space used:    96338
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