GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylH in Escherichia coli BW25113

Align Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate 16257 b2148 beta-methylgalactoside transporter inner membrane component (NCBI)

Query= TCDB::G4FGN4
         (313 letters)



>FitnessBrowser__Keio:16257
          Length = 336

 Score =  190 bits (483), Expect = 4e-53
 Identities = 111/323 (34%), Positives = 175/323 (54%), Gaps = 18/323 (5%)

Query: 9   REAGIFLILIAIVVFLGVTTREFLTVENIFTVILNVSFIAIMSFGMTMVIITSGIDLSVG 68
           +E GI+++L+ ++  +      FL++ N+  ++   S   I++ G+  +I+T G DLS G
Sbjct: 14  KEGGIYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAG 73

Query: 69  SILGAASVVMGLLMD----------EKGLSPF-LSVVIGLAVGVGFGLANGLLITKARLA 117
             +G A+VV   L+           E    P  L ++I  A+G   GL NGL+I    + 
Sbjct: 74  RQVGLAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVT 133

Query: 118 PFISTLGMLSVGRG---LAYVMSGGWPISPFPESFTVHGQGMVGPVPVPVIYMAVIGVIA 174
           PFI+TLG + +  G   L Y   G  PIS F   F+   QG V      + Y+    +IA
Sbjct: 134 PFITTLGTMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGSFRLSYITFYALIA 193

Query: 175 HIFL----KYTVTGRRIYAIGGNMEASKLVGIKTDRILILVYTINGFLAAFAGFLLTAWL 230
             F+      T  G+ I+AIGGN EA+K+ G+     L+++Y ++G   AF G L    +
Sbjct: 194 VAFVWVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAGRI 253

Query: 231 GVAQPNAGQGYELDVIAATVIGGTSLSGGEGTILGAFLGAVIMGVLRNGMILLGVSSFWQ 290
           G A  N G  YELD IAA V+GG S SGG GT++G   G +I  V+  G+  +GV+ +WQ
Sbjct: 254 GSATNNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPYWQ 313

Query: 291 QVVIGIVIIIAIAIDQIRRAKER 313
            ++ G +II A+A+D ++ A+++
Sbjct: 314 YIIKGAIIIFAVALDSLKYARKK 336


Lambda     K      H
   0.328    0.145    0.421 

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: 324
Number of extensions: 16
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: 313
Length of database: 336
Length adjustment: 28
Effective length of query: 285
Effective length of database: 308
Effective search space:    87780
Effective search space used:    87780
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: 48 (23.1 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