GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Roseburia faecis M72

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_055067247.1 M72_RS03765 galactoside ABC transporter permease

Query= uniprot:D8IZC8
         (344 letters)



>NCBI__GCF_001406815.1:WP_055067247.1
          Length = 548

 Score =  135 bits (339), Expect = 3e-36
 Identities = 100/330 (30%), Positives = 159/330 (48%), Gaps = 38/330 (11%)

Query: 39  VVLYLLFYGLTLYLSGDGTSNFASAENTMNILRQVAINLVLAAGMTFVILTAGIDLSVGS 98
           + + L+F  L +       +   +  N +NIL+Q +  + LA G+  +IL  G DLSVG 
Sbjct: 226 IAIILIFVALCIITPIKKGTPLLTYNNILNILQQASPRMFLALGVAGLILLTGTDLSVGR 285

Query: 99  VLAV-----SAVLGMQVSLGAAPGWAI-------PMFIFSGLVMGMV--------NGAMV 138
           ++ +     + ++   V+ G   G          P  +   LV  +V         G   
Sbjct: 286 MVGMGMTTATIIMHQGVNTGGVFGHIFDFTKVPTPARVILALVACIVLCTFFTSIAGFFT 345

Query: 139 ALLNINAFVVTLGTMTAFRGAAYLLADGT-------TVLNNDIPSFEWIGNGDFLHVPWL 191
           A   ++ F+ T+  M    G       G        T+ N  IP      NG     P +
Sbjct: 346 AKFKMHPFISTMANMLVIFGLVTYATKGVSFGAIEPTIPNMVIPKV----NG----FPTI 397

Query: 192 IWVAVAVVLLSWVILRKTVLGMHIYAIGGNLQAARLTGIRVGLVLLFVYSISGLFSGLAG 251
           I  AVA +++ W I  KT  G ++YA+GGN +AA ++GI V  V L  + ++G+  G   
Sbjct: 398 ILWAVAAIVIVWFIWNKTTFGKNLYAVGGNPEAAAVSGISVFAVTLGAFIMAGILYGFGS 457

Query: 252 AMSASRLYGA-NGNWGSGYELDAIAAVVLGGTSLMGGVGSIWGTVVGALIIGVMNNGLTI 310
            +  +R+ G+ +  +G G+++DAIAA V+GG S  GG+G I G V G  I   +   LTI
Sbjct: 458 WLECTRMVGSGSAAYGQGWDMDAIAACVVGGVSFTGGIGKISGVVTGVCIFTALTYSLTI 517

Query: 311 LGLSSFWQYVAKGAVIVLAVILD--KWRQK 338
           LG+ +  Q+V  G +I++AV LD  K+ QK
Sbjct: 518 LGIDTNLQFVFSGIIILVAVTLDCLKYVQK 547


Lambda     K      H
   0.324    0.138    0.417 

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: 367
Number of extensions: 20
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: 344
Length of database: 548
Length adjustment: 32
Effective length of query: 312
Effective length of database: 516
Effective search space:   160992
Effective search space used:   160992
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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