GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Escherichia coli BW25113

Align ABC-type transporter, integral membrane subunit, component of D-ribose porter (Nanavati et al., 2006). Induced by ribose (characterized)
to candidate 16257 b2148 beta-methylgalactoside transporter inner membrane component (NCBI)

Query= TCDB::Q9X050
         (331 letters)



>FitnessBrowser__Keio:16257
          Length = 336

 Score =  204 bits (518), Expect = 3e-57
 Identities = 127/316 (40%), Positives = 175/316 (55%), Gaps = 8/316 (2%)

Query: 24  ILLGLIVLFSFLSNRFLTLENFWIILRQTAVNLCIAVGMTFVILTGGIDLSVGSILGFSG 83
           +LL L+ +  F    FL+L N   IL Q++V + IA+G+  +I+T G DLS G  +G + 
Sbjct: 21  VLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAGRQVGLAA 80

Query: 84  AVTAKLLKYGLILSAFGVVLKFNPLGASIIGVLA-GFAIGLFNGFIITRFNIPPFVATLG 142
            V A LL+     +     +   P+   I+ V A G  IGL NG II   N+ PF+ TLG
Sbjct: 81  VVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVTPFITTLG 140

Query: 143 TMTAVRGFIML---LTKGHPITRLGDSFDFIGSGWF-LG---IPMPVWIAAIATGVGIFI 195
           TM  V G   L        PI+     F     G+  LG   +    + A IA      +
Sbjct: 141 TMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGSFRLSYITFYALIAVAFVWVL 200

Query: 196 LRKTQFGRYVYAVGGNEKAAVLSGVNSKLTKLWVYAISGILSAVAGLIVTARLDSAQPNA 255
             KT+FG+ ++A+GGN +AA +SGVN  L  L +YA+SG+  A  G++   R+ SA  N 
Sbjct: 201 WNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAGRIGSATNNL 260

Query: 256 GLMYELDAIAATVIGGASLSGGKGTLIGTVVGALIIGVLNDGLVLVGVSPFWQQVAKGFI 315
           G MYELDAIAA V+GG S SGG GT+IG V G +I  V+N GL  +GV+P+WQ + KG I
Sbjct: 261 GFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPYWQYIIKGAI 320

Query: 316 IIAAVIAEKLGRGEKE 331
           II AV  + L    K+
Sbjct: 321 IIFAVALDSLKYARKK 336


Lambda     K      H
   0.327    0.144    0.427 

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: 405
Number of extensions: 36
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: 331
Length of database: 336
Length adjustment: 28
Effective length of query: 303
Effective length of database: 308
Effective search space:    93324
Effective search space used:    93324
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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