GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Cupriavidus basilensis 4G11

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate RR42_RS32890 RR42_RS32890 ABC transporter permease

Query= TCDB::P23200
         (336 letters)



>FitnessBrowser__Cup4G11:RR42_RS32890
          Length = 322

 Score =  179 bits (453), Expect = 1e-49
 Identities = 107/317 (33%), Positives = 173/317 (54%), Gaps = 20/317 (6%)

Query: 18  IYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAGRQVG 77
           ++ + L+ L + +  D  FL+L N+ N+L Q+S+  ++A GV  +I+T G DLS G  V 
Sbjct: 21  LFALGLLCLLLAVASD-AFLTLGNILNVLRQASLLFLLASGVTLVILTGGLDLSVGANVA 79

Query: 78  LAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVTPFIT 137
           ++A VAAT+++            AT    L +      GA+IGL NGL++A L + PFI 
Sbjct: 80  MSACVAATVMK------------ATGSTMLGVGAGLGTGALIGLANGLLVAMLRIPPFIA 127

Query: 138 TLGTMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGSFRLSYITFYALIAVAFV 197
           T G + +++G+    Y F+    I GF   F     G++    + +    +  L+ +   
Sbjct: 128 TYGMLWVLHGVT---YWFMAGETIHGFPPAFRAIGSGYL----WGVPIPVYLMLVFLVAG 180

Query: 198 WVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAGRIGSAT 257
             +  KT +G+ I+AIG NP AA++SGV V   L+++Y +SG       ++   R+ SA 
Sbjct: 181 TAMSQKTTYGQEIYAIGANPVAARLSGVPVRRRLVLVYLVSGAMAGIASLVFLARLNSAE 240

Query: 258 NNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPYWQYIIK 317
            ++G    L AIAA ++GG S  GGVG V G + G II T++  G+  + V+  WQ ++ 
Sbjct: 241 GDIGEALTLPAIAAVLIGGTSLFGGVGRVSGTLVGAIILTLVLNGMNLLTVSANWQPLVT 300

Query: 318 GAIIIFAVALDSLKYAR 334
           G I++ AV LD+L   R
Sbjct: 301 GVIVVLAVFLDTLSRKR 317


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: 303
Number of extensions: 19
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: 336
Length of database: 322
Length adjustment: 28
Effective length of query: 308
Effective length of database: 294
Effective search space:    90552
Effective search space used:    90552
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.

Links

Downloads

Related tools

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