GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Pseudomonas putida KT2440

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 PP_2761 PP_2761 putative Ribose ABC transporter, permease protein

Query= TCDB::G4FGN4
         (313 letters)



>FitnessBrowser__Putida:PP_2761
          Length = 328

 Score =  147 bits (372), Expect = 3e-40
 Identities = 94/289 (32%), Positives = 159/289 (55%), Gaps = 9/289 (3%)

Query: 16  ILIAIVVFLGVTTREFLTVENIFTVILN-VSFIAIMSFGMTMVIITSGIDLSVGSILGAA 74
           +  A+++F  +    FLTV N+ +++LN    +AI++ GMT  I   GIDLSVG+ L  +
Sbjct: 29  LFAAVLLFFALKAPGFLTVGNLSSLLLNNFVLLAIVAIGMTYAIAAGGIDLSVGTALDFS 88

Query: 75  SVVMGLLMDEKGLSPFLSVVIGLAVGVGFGLANGLLITKARLAPFISTLGMLSVGRGLAY 134
           ++   LL++  G   ++++  GL  G   GL N  LI   R++PF++TLG L +G  +  
Sbjct: 89  ALTFVLLLNA-GFGLYVAIPGGLLAGSLAGLFNAGLIAGLRISPFLATLGTLFIGSSVQK 147

Query: 135 VMS-GGWPISPFPESFTVHG---QGMVGPVPVPVIYMAVIGVIAHIFLKYTVTGRRIYAI 190
           ++S GG PI  + E+    G   + M+G VP+P++ +A++ ++  + L     GR I  +
Sbjct: 148 LLSEGGQPI--YLEAQVRSGLATERMLG-VPLPLLLVALLALVYGVVLARGRLGREIIVL 204

Query: 191 GGNMEASKLVGIKTDRILILVYTINGFLAAFAGFLLTAWLGVAQPNAGQGYELDVIAATV 250
           G     ++  G+   RI  LV+  + F +A AG LL A +    P +G  + ++ I A  
Sbjct: 205 GSQPLVARYSGLAQRRIAALVFIASAFASALAGILLPATVNAYAPMSGNAFLMNAIGAVF 264

Query: 251 IGGTSLSGGEGTILGAFLGAVIMGVLRNGMILLGVSSFWQQVVIGIVII 299
           IG T        + G  LG + + V  NG++L+G + FWQQV  G++I+
Sbjct: 265 IGATLSLHNRVNVPGTLLGVLFLNVTANGLLLIGWNFFWQQVATGVLIL 313


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: 256
Number of extensions: 22
Number of successful extensions: 4
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: 328
Length adjustment: 28
Effective length of query: 285
Effective length of database: 300
Effective search space:    85500
Effective search space used:    85500
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