GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Lentibacillus jeotgali Grbi

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 WP_010530733.1 ON01_RS09150 ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>NCBI__GCF_000224785.1:WP_010530733.1
          Length = 355

 Score =  161 bits (408), Expect = 2e-44
 Identities = 96/280 (34%), Positives = 152/280 (54%), Gaps = 17/280 (6%)

Query: 4   VTFDKATRIYPGSDKPAVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIR 63
           + F    + YP   K A++   + I +GE + L+GPSGCGK+T+++M+  L +   G I 
Sbjct: 2   IQFSDVKKTYPDGTK-AINDFSLKINEGELVTLIGPSGCGKTTTMKMINRLIEPTAGTIY 60

Query: 64  IGDRDVT--HLPPKDRDIAMVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAK 121
           I   ++   ++     +I  V Q  AL+PHMT+ +N+    ++    + EIR++ EE  +
Sbjct: 61  INGTNINDYNIHELRWNIGYVLQQIALFPHMTIEENIAVVPEMKKWKRKEIRERSEELLE 120

Query: 122 ILDLTQ--YLDRKPKALSGGQRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIA 179
           ++ L    Y+ R+P  LSGG++QRV + RA+  +P + LMDEP S LD   R   +  I 
Sbjct: 121 MVGLNSSTYMHRRPSELSGGEQQRVGVIRALAADPDIILMDEPFSALDPISREQLQHDIK 180

Query: 180 SLQRRLGITTVYVTHDQVEAMTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIG-- 237
            L + +  T V+VTHD  EA+ +GD+V ++K+G + QVD+P+ +   P   FV  FIG  
Sbjct: 181 KLHQEIRKTIVFVTHDIDEALALGDKVCLMKEGRIIQVDTPQQLVLHPETTFVKDFIGER 240

Query: 238 -SPAMNLVEVPITDGGVKFGNSVVPVNREALSAADKGDRT 276
            SP    ++V   D         V       +A DKGD T
Sbjct: 241 KSPWQTAIDVVAGD---------VDSRVITKAAYDKGDYT 271


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: 284
Number of extensions: 11
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: 377
Length of database: 355
Length adjustment: 30
Effective length of query: 347
Effective length of database: 325
Effective search space:   112775
Effective search space used:   112775
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 24 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