GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF in Herbaspirillum seropedicae SmR1

Align D-xylose ABC transporter, periplasmic D-xylose-binding protein (characterized)
to candidate HSERO_RS22460 HSERO_RS22460 xylose ABC transporter substrate-binding protein

Query= CharProtDB::CH_003787
         (330 letters)



>FitnessBrowser__HerbieS:HSERO_RS22460
          Length = 338

 Score =  399 bits (1026), Expect = e-116
 Identities = 198/332 (59%), Positives = 257/332 (77%), Gaps = 5/332 (1%)

Query: 3   IKNILLTLCTSLLLTNVA----AHAKEVKIGMAIDDLRLERWQKDRDIFVKKAESLGAKV 58
           +K  +L L T   L+ VA    A AK  KIG +IDDLR+ERW +DRD F   AE LGAKV
Sbjct: 5   LKKTVLALMTVTTLSMVAGSAMADAKNPKIGFSIDDLRVERWARDRDFFTAAAEKLGAKV 64

Query: 59  FVQSANGNEETQMSQIENMINRGVDVLVIIPYNGQVLSNVVKEAKQEGIKVLAYDRMIND 118
           +VQSA+ +E+ Q+SQIEN+I+RGVDV+VI+P+N  VL+N +KEAK+ GIKVL+YDR+I +
Sbjct: 65  YVQSADASEQRQISQIENLISRGVDVIVIVPFNATVLTNTIKEAKKAGIKVLSYDRLILN 124

Query: 119 ADIDFYISFDNEKVGELQAKALVDIVPQGNYFLMGGSPVDNNAKLFRAGQMKVLKPYVDS 178
           AD+D YISFDNEKVGE+QA+ ++ +  +GN+FL+GGSP DNNAK+FR GQMK LKPY+D 
Sbjct: 125 ADVDAYISFDNEKVGEMQAEGILKVKNKGNFFLLGGSPTDNNAKMFREGQMKALKPYIDK 184

Query: 179 GKIKVVGDQWVDGWLPENALKIMENALTANNNKIDAVVASNDATAGGAIQALSAQGLSGK 238
           G IK+VG QWV  W P  AL I+ENALTANNNKIDA+VASND TAGGAIQAL+AQ L+GK
Sbjct: 185 GDIKIVGQQWVKEWNPTEALSIVENALTANNNKIDAIVASNDGTAGGAIQALAAQKLAGK 244

Query: 239 VAISGQDADLAGIKRIAAGTQTMTVYKPITLLANTAAEIAVELGNGQEPKADTTLNNGLK 298
           V +SGQDADLA +KR+ AGTQTMTVYKP+  +A  AA+++VEL   ++P  +   +NG K
Sbjct: 245 VPVSGQDADLAAVKRVVAGTQTMTVYKPLKQIATEAAKLSVELARNEKPTYNAQYDNGFK 304

Query: 299 DVPSRLLTPIDVNKNNIKDTVIKDGFHKESEL 330
            V S LL PI + K N+K  ++ DGF+ ++++
Sbjct: 305 KVDSLLLKPILLTKENVK-VLVDDGFYTQAQI 335


Lambda     K      H
   0.314    0.132    0.366 

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: 384
Number of extensions: 7
Number of successful extensions: 1
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: 330
Length of database: 338
Length adjustment: 28
Effective length of query: 302
Effective length of database: 310
Effective search space:    93620
Effective search space used:    93620
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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