GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Bradyrhizobium sp. BTAi1

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 WP_012047541.1 BBTA_RS36615 ABC transporter permease

Query= TCDB::G4FGN4
         (313 letters)



>NCBI__GCF_000015165.1:WP_012047541.1
          Length = 330

 Score =  204 bits (518), Expect = 3e-57
 Identities = 111/292 (38%), Positives = 171/292 (58%), Gaps = 1/292 (0%)

Query: 13  IFLILIAIVVFLGVTTREFLTVENIFTVILNVSFIAIMSFGMTMVIITSGIDLSVGSILG 72
           +++  + ++V   +++  FL+V+N   +    + ++I++ GMT +II   IDLSV S L 
Sbjct: 35  LYIAFVILLVVFSLSSPWFLSVDNFLNIGRQTTLVSIIAVGMTFIIIARQIDLSVASTLA 94

Query: 73  AASVVMGLLMDEKGLSPFLSVVIGLAVGVGFGLANGLLITKARLAPFISTLGMLSVGRGL 132
            + +   L M +   S  +  V GL  G   GL NG+L T+  +  F+ TLG LS+ RGL
Sbjct: 95  LSGMAAALAMSQINNSWIVGAVAGLGTGALVGLLNGILTTQLSIPSFLVTLGSLSMARGL 154

Query: 133 AYVMSGGWPISPFPES-FTVHGQGMVGPVPVPVIYMAVIGVIAHIFLKYTVTGRRIYAIG 191
           A +++   P+    E+ F + G+G +  +PVP+ +     ++  + L Y V GRRIYA+G
Sbjct: 155 AMMVTNTKPVIITNETYFAIFGEGTLLGIPVPIAWTLAAMIVGILLLHYNVFGRRIYAVG 214

Query: 192 GNMEASKLVGIKTDRILILVYTINGFLAAFAGFLLTAWLGVAQPNAGQGYELDVIAATVI 251
           GN  A+   GI T  I    + + G LA  A  +L+A    A+P+  QG ELDVIAA ++
Sbjct: 215 GNPTAALYSGINTKLITTAAFVLTGTLAGLAALVLSARSHAARPDVVQGMELDVIAAVIL 274

Query: 252 GGTSLSGGEGTILGAFLGAVIMGVLRNGMILLGVSSFWQQVVIGIVIIIAIA 303
           GG SL GG G ILG   G++I+G L NG++LLGVSS  Q V+ G +I+ A+A
Sbjct: 275 GGCSLFGGRGYILGTLFGSLIIGTLNNGLVLLGVSSPMQLVIKGAIIVAAVA 326


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: 290
Number of extensions: 13
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: 313
Length of database: 330
Length adjustment: 28
Effective length of query: 285
Effective length of database: 302
Effective search space:    86070
Effective search space used:    86070
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 Apr 09 2024. 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