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_RS18590 RR42_RS18590 hypothetical protein

Query= TCDB::P96483
         (377 letters)



>FitnessBrowser__Cup4G11:RR42_RS18590
          Length = 359

 Score =  316 bits (809), Expect = 7e-91
 Identities = 185/360 (51%), Positives = 228/360 (63%), Gaps = 30/360 (8%)

Query: 24  LDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKDRDIAMVF 83
           +DI I DG+F VLVGPSGCGKST LRM+AGLE++  G I IG+R V  LPPK+RDIAMVF
Sbjct: 22  VDIDIADGQFTVLVGPSGCGKSTLLRMIAGLEEITTGEIAIGNRVVNRLPPKERDIAMVF 81

Query: 84  QNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKALSGGQRQR 143
           QNYALYPHMTV DNM F+LK+A   K EI++KV +A+ IL L   L+R P+ LSGGQRQR
Sbjct: 82  QNYALYPHMTVYDNMAFSLKLAKGDKEEIKRKVAKASAILGLDSLLERYPRQLSGGQRQR 141

Query: 144 VAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQVEAMTMG 203
           VAMGRAIVR+PQVFL DEPLSNLDAKLRV  R +I  L +RL  T+VYVTHDQ+EAMTM 
Sbjct: 142 VAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRAEIKELHQRLRTTSVYVTHDQIEAMTMA 201

Query: 204 DRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPIT----DGGVKFGNSV 259
           D++ V++DG ++Q   P  +YD P NLFVAGFIGSPAMN V   +     D  V+F +  
Sbjct: 202 DQIVVMRDGRVEQRGKPLALYDHPDNLFVAGFIGSPAMNFVPGVLRRSGGDAAVEFPDGT 261

Query: 260 ---VPVNREALSAADKGDRTVTVGVRPEHFDVVELGGAVAASLSKDSADAPAGLAVSVNV 316
               P   +A +  D G R V  GVRPEH  +   G                GL   V+V
Sbjct: 262 RLPAPARFDATAGTD-GQR-VIYGVRPEHLTLGMPG---------------QGLQTRVSV 304

Query: 317 VEELGADGYVYGT-AEVGGEVKDLVVRVNGRQVPEKGSTLHVVPRPGETHVFSTSTGERL 375
           VE  GA+  +Y    E      + +     R     G  L++VP    TH+F   +G+ L
Sbjct: 305 VEPTGANTEIYSRFCEA-----EFISIFRERHDFAAGDILNLVPDHQHTHLFDADSGQTL 359


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: 417
Number of extensions: 26
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: 359
Length adjustment: 30
Effective length of query: 347
Effective length of database: 329
Effective search space:   114163
Effective search space used:   114163
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.

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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