GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Herbaspirillum seropedicae SmR1

Align Fructose import permease protein FruG (characterized)
to candidate HSERO_RS05255 HSERO_RS05255 ribose ABC transporter permease

Query= SwissProt::Q8G845
         (340 letters)



>FitnessBrowser__HerbieS:HSERO_RS05255
          Length = 347

 Score =  159 bits (402), Expect = 1e-43
 Identities = 100/305 (32%), Positives = 166/305 (54%), Gaps = 5/305 (1%)

Query: 26  LAAVVIFILMIIMGQALFGTYIRLGFISSLFIDHAYLIILAVAMTLPILTGGIDLSVGAI 85
           L A    +LMI+        ++ +  + S+    A   +LA+A T  I+T GIDLSVG +
Sbjct: 37  LLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVGTM 96

Query: 86  VAITAVV-GLKLANAGVPAFLVMIIMLLIGAVFGLLAGTLIEEFNMQPFIATLSTMFLAR 144
           +   AV+ G+ L N G+P  L +   +  GA+ G ++G +I +  + PFIATL  M L +
Sbjct: 97  MTFCAVMAGVVLTNWGMPLPLGIAAAIFFGALSGWISGMVIAKLKVPPFIATLGMMMLLK 156

Query: 145 GLASIIS-TDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFNVGVIIALVVVVFGYVFLH 203
           GL+ +IS T  + F     FS I+    I D   +   L     V+I  +V +   + L+
Sbjct: 157 GLSLVISGTRPIYFNDTEGFSAIAQDSLIGD---LIPSLPIPNAVLILFLVAIGASIILN 213

Query: 204 HTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAALASIVYTANIGSAKNTVGV 263
            T  GR  +A+G +  +  L G+ V   +  +Y  S  +  +A ++  + + SA+  +G 
Sbjct: 214 KTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASRLNSAQPALGQ 273

Query: 264 GWELDAVASVVIGGTIITGGFGYVLGSVLGSLVRSILDPLTSDFGVPAEWTTIVIGLMIL 323
           G+ELDA+A+VVIGGT ++GG G +LG+++G+ + S+L        V  EW T+V G++I+
Sbjct: 274 GYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEWQTVVTGVIII 333

Query: 324 VFVVL 328
           + V L
Sbjct: 334 LAVYL 338


Lambda     K      H
   0.327    0.142    0.400 

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: 250
Number of extensions: 11
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: 340
Length of database: 347
Length adjustment: 29
Effective length of query: 311
Effective length of database: 318
Effective search space:    98898
Effective search space used:    98898
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