GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Rhodobacter viridis JA737

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate WP_110805878.1 C8J30_RS10880 ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>NCBI__GCF_003217355.1:WP_110805878.1
          Length = 352

 Score =  176 bits (445), Expect = 1e-48
 Identities = 102/334 (30%), Positives = 173/334 (51%), Gaps = 9/334 (2%)

Query: 22  ALPASRGKRARSELARLRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVV 81
           A PAS   +    L  L +     AL L+    AF++P+FL+ AN + V   +A  A + 
Sbjct: 3   AAPASTPAQGSPLLLTLLQARTYLALILVFGFFAFMAPNFLSVANSVIVAKHAALTAFLA 62

Query: 82  LAESLIVLTGKFDLSLESTVGIAPAVGAMLVMPAASAGF--GMQWPAAAGLLAIVVVGAV 139
           +  + +++TG  DLS+ STVG+   V   L++     G    MQ+      L ++ VG  
Sbjct: 63  IGMTFVIITGGIDLSVGSTVGLCAMVSGWLILYGIDLGAMGTMQFNTLEIALLVMCVGVF 122

Query: 140 IGFINGFLVVRLRLNAFIVTLAMLIVLRGMLVGATKGGTLFDMP-------TSFFALATT 192
           +GF+NG L+ +L +  FI TL  L + RG  + ++ G T  ++         SF  +   
Sbjct: 123 VGFVNGILITKLNVAPFIATLGTLYIARGAALLSSGGRTFPNLSGNADYGSASFPGIGAG 182

Query: 193 IVLGLPLSVWLAAAAFAIAAFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLG 252
             LGLP+ +W+  A   +AA++ +   LGR +YA+GGN   A  +G++V R+   V++  
Sbjct: 183 TFLGLPVQIWMLIAVGLVAAYIAKRTPLGRHIYAVGGNERGAALSGVKVNRVKLFVYMFS 242

Query: 253 SILASVGGLIVTGYVGAINANQGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGV 312
              A++ GLI+   + A +   G        AAAV+GG SL GG+G + G + G  ++ +
Sbjct: 243 GFCAAIVGLIIASQLQAAHPATGETFELNAIAAAVLGGTSLSGGRGKIGGTIVGAFVISI 302

Query: 313 VQNLLTLAQVPSFWIQAIYGAIILGSLMVARLAS 346
           + + L +  V SFW   I G +I+ ++++ +  S
Sbjct: 303 LSDGLVMMSVSSFWQTVIKGLVIVAAVVIDQAQS 336


Lambda     K      H
   0.326    0.140    0.397 

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: 284
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: 351
Length of database: 352
Length adjustment: 29
Effective length of query: 322
Effective length of database: 323
Effective search space:   104006
Effective search space used:   104006
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 (21.6 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