GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Bradyrhizobium sp. BTAi1

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_041750694.1 BBTA_RS16625 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= TCDB::P96483
         (377 letters)



>NCBI__GCF_000015165.1:WP_041750694.1
          Length = 353

 Score =  341 bits (874), Expect = 2e-98
 Identities = 186/351 (52%), Positives = 233/351 (66%), Gaps = 22/351 (6%)

Query: 26  IAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKDRDIAMVFQN 85
           I IEDGEF+VLVGPSGCGKST LRMLAGLE++  G I IG+R V ++ PK+RDIAMVFQN
Sbjct: 24  IPIEDGEFVVLVGPSGCGKSTLLRMLAGLENITSGTISIGERVVNNVQPKERDIAMVFQN 83

Query: 86  YALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKALSGGQRQRVA 145
           YALYPHMTVADNMGF+LK+ G    +I++ V  AA+IL LT  LDR P+ LSGGQRQRVA
Sbjct: 84  YALYPHMTVADNMGFSLKLRGARPEDIKKGVARAAEILALTPLLDRYPRQLSGGQRQRVA 143

Query: 146 MGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQVEAMTMGDR 205
           MGRAIVR+PQVFL DEPLSNLDAKLRV+ RT+I  L +RL  TTVYVTHDQ+EAMTM D+
Sbjct: 144 MGRAIVRDPQVFLFDEPLSNLDAKLRVAMRTEIKELHQRLKTTTVYVTHDQIEAMTMADK 203

Query: 206 VAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPITDGGVKFGNSVVPVNRE 265
           + V+ DG+++Q+ SP ++YDKP N FVAGFIGSPAMN +   +   G  +  +       
Sbjct: 204 IVVMHDGIVEQMGSPLDLYDKPDNQFVAGFIGSPAMNFLNGHLKSNGTVYVETDNGAKLP 263

Query: 266 ALSA-ADKGDRTVTVGVRPEHFDVVELGGAVAASLSKDSADAPAGLAVSVNVVEELGADG 324
            L+A A    R V  GVRPEH ++                 A  G+   V VVE  G++ 
Sbjct: 264 LLTAPAASNGRPVVYGVRPEHLEL-----------------ADDGIEAEVVVVEPTGSET 306

Query: 325 YVYGTAEVGGEVKDLVVRVNGRQVPEKGSTLHVVPRPGETHVFSTSTGERL 375
            +   A +G   +D++     R     G+ +H+ PR    H+F   TG RL
Sbjct: 307 QI--VARIG--TQDIIAVFRDRHEVVPGAKIHLRPRASAAHLFDKDTGRRL 353


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: 406
Number of extensions: 22
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: 353
Length adjustment: 30
Effective length of query: 347
Effective length of database: 323
Effective search space:   112081
Effective search space used:   112081
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 Apr 09 2024. 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