GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Pseudomonas fluorescens GW456-L13

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate PfGW456L13_2122 L-arabinose transport system permease protein (TC 3.A.1.2.2)

Query= TCDB::P23200
         (336 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2122
          Length = 323

 Score =  166 bits (419), Expect = 1e-45
 Identities = 108/315 (34%), Positives = 163/315 (51%), Gaps = 26/315 (8%)

Query: 17  GIYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAGRQV 76
           GI+V   +L+         FLS LN+  +    S   I A  +   + +   DLS G  +
Sbjct: 33  GIFVACTLLI-------DNFLSPLNMRGLGLAISTTGIAACTMLYCLASGHFDLSVGSVI 85

Query: 77  GLAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVTPFI 136
             A VVAA +++   + N VF         L +     +G ++GLING++IA L V   I
Sbjct: 86  ACAGVVAAVVMR---DTNSVF---------LGVCAALVMGLIVGLINGIVIAKLRVNALI 133

Query: 137 TTLGTMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGSFRLSYITFYALIAVAF 196
           TTL TM IV G   L Y F     +      F  F  G +    F +       ++   F
Sbjct: 134 TTLATMQIVRG---LAYIFANGKAVGVSQESFFVFGNGQM----FGVPVPILITIVCFLF 186

Query: 197 VWVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAGRIGSA 256
              L N T +G+N  AIGGN EAA ++GVNV    ++I+A+ GV  A  G++ A R+ S 
Sbjct: 187 FGWLLNYTTYGRNTMAIGGNQEAALLAGVNVDRTKIIIFAVHGVIGALAGVILASRMTSG 246

Query: 257 TNNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPYWQYII 316
              +G  +EL  I+ACV+GGVS SGG+G +  V+ GV+I  +I   +    ++ ++QY+I
Sbjct: 247 QPMIGQGFELTVISACVLGGVSLSGGIGMIRHVIAGVLILAIIENAMNLKNIDTFYQYVI 306

Query: 317 KGAIIIFAVALDSLK 331
           +G+I++ AV +D LK
Sbjct: 307 RGSILLLAVVIDRLK 321


Lambda     K      H
   0.327    0.143    0.415 

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: 274
Number of extensions: 15
Number of successful extensions: 5
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: 336
Length of database: 323
Length adjustment: 28
Effective length of query: 308
Effective length of database: 295
Effective search space:    90860
Effective search space used:    90860
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