GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Rhodobacter viridis JA737

Align Fructose import permease protein FruG (characterized)
to candidate WP_110805878.1 C8J30_RS10880 ABC transporter permease

Query= SwissProt::Q8G845
         (340 letters)



>NCBI__GCF_003217355.1:WP_110805878.1
          Length = 352

 Score =  153 bits (386), Expect = 7e-42
 Identities = 112/342 (32%), Positives = 175/342 (51%), Gaps = 24/342 (7%)

Query: 5   TANKVKAPKKGFKLDRQMIPTLAAVVIFILMIIMGQALFGTYIRLGFISSLFI-DHAYLI 63
           TA     P +G  L   ++  L A     L+++ G   F     L   +S+ +  HA L 
Sbjct: 2   TAAPASTPAQGSPL---LLTLLQARTYLALILVFGFFAFMAPNFLSVANSVIVAKHAALT 58

Query: 64  -ILAVAMTLPILTGGIDLSVGAIVAITAVV-------GLKLANAGVPAFLVMIIMLLI-- 113
             LA+ MT  I+TGGIDLSVG+ V + A+V       G+ L   G   F  + I LL+  
Sbjct: 59  AFLAIGMTFVIITGGIDLSVGSTVGLCAMVSGWLILYGIDLGAMGTMQFNTLEIALLVMC 118

Query: 114 -GAVFGLLAGTLIEEFNMQPFIATLSTMFLARGLASIISTDSLTFPQ--GN-DFSFISNV 169
            G   G + G LI + N+ PFIATL T+++ARG A+++S+   TFP   GN D+   S  
Sbjct: 119 VGVFVGFVNGILITKLNVAPFIATLGTLYIARG-AALLSSGGRTFPNLSGNADYGSAS-- 175

Query: 170 IKIIDNPKISNDLSFNVGVIIALVVVVFGYVFLHHTRTGRTIYAIGGSRSSAELMGLPVK 229
                       L   V + + + V +        T  GR IYA+GG+   A L G+ V 
Sbjct: 176 ---FPGIGAGTFLGLPVQIWMLIAVGLVAAYIAKRTPLGRHIYAVGGNERGAALSGVKVN 232

Query: 230 RTQYIIYLTSATLAALASIVYTANIGSAKNTVGVGWELDAVASVVIGGTIITGGFGYVLG 289
           R +  +Y+ S   AA+  ++  + + +A    G  +EL+A+A+ V+GGT ++GG G + G
Sbjct: 233 RVKLFVYMFSGFCAAIVGLIIASQLQAAHPATGETFELNAIAAAVLGGTSLSGGRGKIGG 292

Query: 290 SVLGSLVRSILDPLTSDFGVPAEWTTIVIGLMILVFVVLQRA 331
           +++G+ V SIL        V + W T++ GL+I+  VV+ +A
Sbjct: 293 TIVGAFVISILSDGLVMMSVSSFWQTVIKGLVIVAAVVIDQA 334


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: 280
Number of extensions: 13
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: 352
Length adjustment: 29
Effective length of query: 311
Effective length of database: 323
Effective search space:   100453
Effective search space used:   100453
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 24 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