GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Cupriavidus basilensis 4G11

Align MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized)
to candidate RR42_RS27800 RR42_RS27800 ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>FitnessBrowser__Cup4G11:RR42_RS27800
          Length = 357

 Score =  227 bits (578), Expect = 4e-64
 Identities = 136/322 (42%), Positives = 193/322 (59%), Gaps = 20/322 (6%)

Query: 20  AVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVN-GGAIRIGDRDVTHLPPKDRD 78
           A+  LD+ I  GE +VL+GPSGCGK+T+LR++AGLE  + GG +  GD DVT LP + R 
Sbjct: 22  ALQPLDLDIGAGETVVLLGPSGCGKTTTLRIIAGLEFPDAGGVVMFGDNDVTPLPIEQRG 81

Query: 79  IAMVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKALSG 138
           + MVFQ+YAL+P+MTVA+N+ + L++  +  A  R++V+E   ++ L  + +R+   LSG
Sbjct: 82  VGMVFQSYALFPNMTVAENIAYGLRVRRIDAAARRRRVDEMLAMMHLGPFAERRIDQLSG 141

Query: 139 GQRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQVE 198
           GQRQRVA+ RAI  +P+V L+DEPL+ LDAKLR + R  I  L R L IT VYVTHDQ E
Sbjct: 142 GQRQRVALARAIAVQPRVLLLDEPLTALDAKLRDALRADINQLLRSLHITAVYVTHDQAE 201

Query: 199 AMTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPITDGGVKFGNS 258
           AM +GDR+ V+  G + Q  +P+ +Y  PAN FVA FIG+  MN +   +     +    
Sbjct: 202 AMALGDRIIVMDRGRIAQTGTPQQIYRAPANAFVADFIGT--MNRLPAVLEADAWRVPGG 259

Query: 259 VVPVNREALSAADKGDRTVTVGVRPEHFDVVE-----LGGAVAASLSKDS-------ADA 306
           +VP +  A S A        +  RPE   + +     LGG+V  +L   +         A
Sbjct: 260 LVPRHGTAASLAAAPSPRAELLFRPEDVALAQAEDAHLGGSVVTALFLGNYTRLLVDVGA 319

Query: 307 PAGLAVSVNVVEELGADGYVYG 328
           PA L     VV+    DG++ G
Sbjct: 320 PAPL-----VVDTTRRDGWLAG 336


Lambda     K      H
   0.317    0.135    0.379 

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: 360
Number of extensions: 15
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: 377
Length of database: 357
Length adjustment: 30
Effective length of query: 347
Effective length of database: 327
Effective search space:   113469
Effective search space used:   113469
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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