GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Pseudomonas simiae WCS417

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate GFF2674 PS417_13640 ribose ABC transporter permease

Query= TCDB::P23200
         (336 letters)



>FitnessBrowser__WCS417:GFF2674
          Length = 325

 Score =  197 bits (500), Expect = 4e-55
 Identities = 122/316 (38%), Positives = 176/316 (55%), Gaps = 26/316 (8%)

Query: 17  GIYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAGRQV 76
           G+  VL++LL         FL++ NLS I  Q+SV +++A G+  +I+T G DLS G  +
Sbjct: 23  GMLPVLILLLVGFALASENFLTMQNLSIISQQASVNVVLAAGMTFVILTAGIDLSVGAIL 82

Query: 77  GLAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVTPFI 136
             +AVVA     S        P+     IA  I      G ++GL+NG +IA++ + PFI
Sbjct: 83  AASAVVALQASMS--------PQFGMFGIAAGI----GFGLLLGLVNGGLIAFMRLPPFI 130

Query: 137 TTLGTMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGSFRLSYITFYALIAVAF 196
            TLG +  + G+  L  D          D         F  +G+  L  + +  +IAVA 
Sbjct: 131 VTLGALTAMRGLARLLAD----------DKTVFNPDLPFAFIGNDSLLGVPWLVIIAVAV 180

Query: 197 V---WVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAGRI 253
           V   W +  +T  G  I+++GGNPEAA++SG+ V   LL +YA+SG     G ++ A R+
Sbjct: 181 VALSWFILRRTVMGVQIYSVGGNPEAARLSGIKVWKVLLFVYAMSGALAGLGAVMSASRL 240

Query: 254 GSATN-NLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPYW 312
            +A    LG  YELDAIAA ++GG SF+GGVGT+ G + G +I  V+  GL  +GV+  W
Sbjct: 241 FAANGLQLGQSYELDAIAAVILGGTSFTGGVGTIGGTLIGALIIAVLTNGLVLLGVSDIW 300

Query: 313 QYIIKGAIIIFAVALD 328
           QYIIKG +II AVALD
Sbjct: 301 QYIIKGIVIIGAVALD 316


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: 297
Number of extensions: 16
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: 336
Length of database: 325
Length adjustment: 28
Effective length of query: 308
Effective length of database: 297
Effective search space:    91476
Effective search space used:    91476
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