GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Hyphomicrobium sulfonivorans WDL6

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_083509566.1 APY04_RS07015 ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>NCBI__GCF_001541235.1:WP_083509566.1
          Length = 392

 Score =  179 bits (455), Expect = 9e-50
 Identities = 108/285 (37%), Positives = 163/285 (57%), Gaps = 14/285 (4%)

Query: 2   ATVTFDKATRIYPGSDKPAVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGA 61
           A +TF+   R +  +   A+  + + I+ GE + L+GPSGCGK+T LR+ AG+E   GG 
Sbjct: 44  ACLTFEDVRRNFGTTQ--ALAGVSLEIDRGEVVCLLGPSGCGKTTLLRIAAGIERPTGGR 101

Query: 62  IRIGDRDV----THLPPKDRDIAMVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVE 117
           + I   +V    + + P+ R + ++FQ++AL+PH+T+A N+ F LK   +P+AE +++  
Sbjct: 102 VLINGHEVAGPSSFVVPEKRSVGLMFQDFALFPHLTIAGNVAFGLK--SLPRAEAKREAL 159

Query: 118 EAAKILDLTQYLDRKPKALSGGQRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQ 177
            A K + L    D  P  LSGGQ+QRVA+ RA+V  P V LMDEP S LD +LR + + +
Sbjct: 160 AALKRVGLEHMADEYPHVLSGGQQQRVALARALVPRPAVMLMDEPFSGLDVQLRDAMQEE 219

Query: 178 IASLQRRLGITTVYVTHDQVEAMTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIG 237
             SL R  G T + VTH+  EAM +GDR+ V++ G L Q      +Y +PA+LFVA    
Sbjct: 220 TLSLLRETGATAMVVTHNPEEAMRIGDRIVVMRAGGLIQQGQAEALYHQPADLFVARLFS 279

Query: 238 SPAMNLVEVPITDGGVKFGNSVVPVNREALSAADKGDRTVTVGVR 282
                + EV    G    G    P+ + +  A  +    VT+GVR
Sbjct: 280 ----EINEVAYRVGA--DGKIDTPIGKLSPPAGLQAHDAVTIGVR 318


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: 385
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: 377
Length of database: 392
Length adjustment: 30
Effective length of query: 347
Effective length of database: 362
Effective search space:   125614
Effective search space used:   125614
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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