GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Rhodobacter viridis JA737

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate WP_110805878.1 C8J30_RS10880 ABC transporter permease

Query= SwissProt::P39328
         (341 letters)



>NCBI__GCF_003217355.1:WP_110805878.1
          Length = 352

 Score =  155 bits (391), Expect = 2e-42
 Identities = 101/315 (32%), Positives = 160/315 (50%), Gaps = 26/315 (8%)

Query: 26  VALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPVALLAIGMTLVIATGGIDLS 85
           +AL+LV    + +AP+F  V         + + +   AA  A LAIGMT VI TGGIDLS
Sbjct: 26  LALILVFGFFAFMAPNFLSVA--------NSVIVAKHAALTAFLAIGMTFVIITGGIDLS 77

Query: 86  VGAVMAIA----------GATTAAMTVAGFSLPIVLLSALGTGILAGLWNGILVAILKIQ 135
           VG+ + +           G    AM    F+   + L  +  G+  G  NGIL+  L + 
Sbjct: 78  VGSTVGLCAMVSGWLILYGIDLGAMGTMQFNTLEIALLVMCVGVFVGFVNGILITKLNVA 137

Query: 136 PFVATLILMVAGRGVAQLITAGQI-------VTFNSPDLSWFGSGSLLFLPTPVIIAVLT 188
           PF+ATL  +   RG A L + G+          + S      G+G+ L LP  + + +  
Sbjct: 138 PFIATLGTLYIARGAALLSSGGRTFPNLSGNADYGSASFPGIGAGTFLGLPVQIWMLIAV 197

Query: 189 LILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVAADI 248
            ++   + ++T LG  I AVG N R A  +GV    + +  Y+ SG CAAI G+I+A+ +
Sbjct: 198 GLVAAYIAKRTPLGRHIYAVGGNERGAALSGVKVNRVKLFVYMFSGFCAAIVGLIIASQL 257

Query: 249 RGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFPPEM 308
           + A     G   EL+AI A V+GG SL GGR  +  ++VGA +I  ++ G+++       
Sbjct: 258 QAAHP-ATGETFELNAIAAAVLGGTSLSGGRGKIGGTIVGAFVISILSDGLVMMSVSSFW 316

Query: 309 NQVVKAVVVLCVLIV 323
             V+K +V++  +++
Sbjct: 317 QTVIKGLVIVAAVVI 331


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: 286
Number of extensions: 12
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: 341
Length of database: 352
Length adjustment: 29
Effective length of query: 312
Effective length of database: 323
Effective search space:   100776
Effective search space used:   100776
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