GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Phaeobacter inhibens BS107

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate GFF2276 PGA1_c23080 ribose transport system permease protein RbsC

Query= uniprot:D8IZC8
         (344 letters)



>FitnessBrowser__Phaeo:GFF2276
          Length = 324

 Score =  186 bits (473), Expect = 5e-52
 Identities = 108/299 (36%), Positives = 166/299 (55%), Gaps = 7/299 (2%)

Query: 37  VLVVLYLLFYGLTLYLSGDGTSNFASAENTMNILRQVAINLVLAAGMTFVILTAGIDLSV 96
           +L+   L   G T+         F + +N  N++R  AI  V+A G+TFV+++  +DLSV
Sbjct: 18  ILIAFALFIIGFTI-----ANPKFLTLDNFENVVRSSAILGVMALGVTFVVISGNLDLSV 72

Query: 97  GSVLAVSAVLGMQVSLGAAPGWAIPMFIFSGLVMGMVNGAMVALLNINAFVVTLGTMTAF 156
           GS+++ S ++ + +     P  AIP      L +G + G +V  L +N+ +VTLG ++A 
Sbjct: 73  GSMMSFSTIVVLDLHDKLGPTLAIPAMFAMTLCLGALIGFLVGYLKLNSLIVTLGMLSAI 132

Query: 157 RGAAYLLADGTT--VLNNDIPSFEWIGNGDFLHVPWLIWVAVAVVLLSWVILRKTVLGMH 214
            G     + G    + + +   F   G G+ L +   I + +A+  L  +IL KT  G  
Sbjct: 133 HGLTLTYSGGKNMDIADKEGTWFAIFGQGNILGIQTPILIFIALAALLGIILAKTPFGRK 192

Query: 215 IYAIGGNLQAARLTGIRVGLVLLFVYSISGLFSGLAGAMSASRLYGANGNWGSGYELDAI 274
           +YA+GGN  AA  +GIR   V+   Y +S L    AG + ASR  G+    G G EL+ +
Sbjct: 193 VYAVGGNGTAATFSGIRRARVVFLCYIMSALCVATAGLIQASRSMGSQNTVGQGLELEVL 252

Query: 275 AAVVLGGTSLMGGVGSIWGTVVGALIIGVMNNGLTILGLSSFWQYVAKGAVIVLAVILD 333
           AAV+LGG SL+GG G+I+ TV+G LI+G + NGL ++GL    QYV    +I+LAV LD
Sbjct: 253 AAVILGGASLLGGSGTIFKTVIGVLILGFIQNGLLLVGLDFSVQYVVTWIIIILAVWLD 311


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: 313
Number of extensions: 24
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: 344
Length of database: 324
Length adjustment: 28
Effective length of query: 316
Effective length of database: 296
Effective search space:    93536
Effective search space used:    93536
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: 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