GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03635 in Tistlia consotensis USBA 355

Align ABC-type sugar transport system, periplasmic component protein (characterized, see rationale)
to candidate WP_089229763.1 B9O00_RS13770 sugar ABC transporter substrate-binding protein

Query= uniprot:D8IZC6
         (316 letters)



>NCBI__GCF_900177295.1:WP_089229763.1
          Length = 333

 Score = 99.4 bits (246), Expect = 1e-25
 Identities = 86/299 (28%), Positives = 138/299 (46%), Gaps = 24/299 (8%)

Query: 8   IACSTLLLAAAAQPAMAADKPLKSVGVTVGDLANPFFVAIAKGAESGAHKINPDAKVTVV 67
           +A + L    AA PA AAD     VG+      NPFFV + +GAE+ A ++  + +    
Sbjct: 1   MASTVLAACLAAGPAAAADT---IVGLVTKTNTNPFFVKMREGAEAKAKELGVELRSYAG 57

Query: 68  SSKYDLNTQVGQIENFIANKVDLIVLNAADSKGVGPAVKKAQKAGIVVVAVDV---AAAG 124
               D+ +QV  IE+ IA     I++  +DS  V PA+ +A+KAG++V+A+D     A+ 
Sbjct: 58  KYDGDVESQVEAIESLIAAGAKGILITPSDSAAVVPALARARKAGLLVIALDTPLDPASA 117

Query: 125 ADVTVMSDNTMAGAESCKFLAEKLQGKGN-----VVIVNGPPVSAVMDRVTGCKAEFKKS 179
           AD T  +DN  AG    ++   +L  K       ++ +N   +S  + R  G    F   
Sbjct: 118 ADATFATDNFKAGQLIGEWAKARLGDKAEDAKIAMLDLNANQISVDVARDQGFLEGFGID 177

Query: 180 PG-IKILSDNQN--------AGGSRDGGMTTMSNLLAAQPKIDAVFAINDPTAIGAELAI 230
            G  K + D ++          G+ +GG   M NL+   P ++ V+ IN+P A GA  A+
Sbjct: 178 IGNPKQIGDEKDGRIVGHDITQGAEEGGRRAMENLMQRNPSLNLVYTINEPAAAGAYEAL 237

Query: 231 RQAKRSDIKWISGVDGAPDAERALKDSKSLFAASPAQDPYGMAAESV--AIGYAVMNGR 287
           R         I  +DG     + +K    +  A+  Q P  MA+  +   + YA    R
Sbjct: 238 RSFGLDSQATIVSIDGGCPGVKNVK--AGVIGATSMQFPLRMASLGIEAVVDYARTGAR 294


Lambda     K      H
   0.314    0.129    0.360 

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: 227
Number of extensions: 11
Number of successful extensions: 2
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: 316
Length of database: 333
Length adjustment: 28
Effective length of query: 288
Effective length of database: 305
Effective search space:    87840
Effective search space used:    87840
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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