GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylH in Rhodobacter johrii JA192

Align D-xylose ABC transporter, permease protein (characterized)
to candidate WP_069330985.1 C8J29_RS17295 ABC transporter permease

Query= CharProtDB::CH_024441
         (393 letters)



>NCBI__GCF_003046325.1:WP_069330985.1
          Length = 412

 Score =  211 bits (538), Expect = 2e-59
 Identities = 128/377 (33%), Positives = 214/377 (56%), Gaps = 5/377 (1%)

Query: 19  FSGLKSLNLQVFVMIAAIIAIMLFFTWTTDGAYLSARNVSNLLRQTAITGILAVGMVFVI 78
           F  ++S +L +  ++  ++ I   F+ T +  +L+  N+ NLL   A  G +++G+V V+
Sbjct: 29  FDRVRSGDLGMLPVLVGLVVISTVFS-TLNPVFLAPNNLVNLLFDAATVGFISLGIVCVL 87

Query: 79  ISAEIDLSVGSMMGLLGGVAAICDVWLGWPLPLTIIVTLVLGLLLGAWNGWWVAYRKVPS 138
           +  +IDLSVGSM GL   +  +  V +GWPLP  I   L  G L+G   G  +    +PS
Sbjct: 88  MLGQIDLSVGSMSGLASAMIGVLWVNMGWPLPAAIAAALGFGALVGLLYGVLLNRFGMPS 147

Query: 139 FIVTLAGMLAFRGILIGI--TNGTTVSPTSAAMSQIGQSY-LPASTGFIIGALGLMAFVG 195
           F+ TLAG+LA  G+ + I    G+   P ++ + + GQ Y +P    +++  L     V 
Sbjct: 148 FVSTLAGLLALLGLQLYILGPTGSINLPYASVLVRFGQIYVMPDWLSYLLALLPGAVLVY 207

Query: 196 WQWRGRMRRQALGLQSPASTAVVGRQALTAIIVLGAIWLLNDYRGVPTPVLLLTLLLLGG 255
              R   RR+A  L SP  + ++ +  +    +L A + LN  RG+P    L   L+L  
Sbjct: 208 TGLRTMARRRAANLSSPGLSVLLVKALVLTAALLFAAYYLNLGRGIPWMFGLFVALVLAM 267

Query: 256 MFMATRTAFGRRIYAIGGNLEAARLSGINVERTKLAVFAINGLMVAIAGLILSSRLGAGS 315
            +  TRT +GR ++A+GGN EAAR SGI+V R  ++ F +   + A+ G++ S+RL + S
Sbjct: 268 NYGLTRTQWGRSMFAVGGNAEAARRSGIDVRRVNVSAFMLCSTLAALGGILASARLASSS 327

Query: 316 PSAG-NIAELDAIAACVIGGTSLAGGVGSVAGAVMGAFIMASLDNGMSMMDVPTFWQYIV 374
             AG     L+AIAA VIGGTSL GG GS   A++G  ++ ++ NG++++++ +  +Y++
Sbjct: 328 QQAGTGDVNLNAIAAAVIGGTSLFGGRGSAYSALLGILVIQAISNGLTLLNLSSSLRYMI 387

Query: 375 KGAILLLAVWMDSATKR 391
            G +L +AV +DS  ++
Sbjct: 388 TGGVLAIAVIVDSLARQ 404


Lambda     K      H
   0.325    0.138    0.415 

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: 394
Number of extensions: 15
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 393
Length of database: 412
Length adjustment: 31
Effective length of query: 362
Effective length of database: 381
Effective search space:   137922
Effective search space used:   137922
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: 50 (23.9 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