GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Pseudomonas fluorescens FW300-N2E3

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 AO353_25895 AO353_25895 ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_25895
          Length = 367

 Score =  297 bits (761), Expect = 3e-85
 Identities = 165/358 (46%), Positives = 220/358 (61%), Gaps = 35/358 (9%)

Query: 24  LDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKDRDIAMVF 83
           +D+ + D EF+V VGPSGCGKST LR++AGLE+V  G I +  RD+T + P  RD+AMVF
Sbjct: 22  IDLEVNDREFVVFVGPSGCGKSTLLRLIAGLEEVTAGTIELDGRDITEVSPAKRDLAMVF 81

Query: 84  QNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKALSGGQRQR 143
           Q YALYPHM+V  NM FAL +AGV KAE+ +KV EAA+IL+L   L+RKPK LSGGQRQR
Sbjct: 82  QTYALYPHMSVRKNMSFALDLAGVNKAEVEKKVNEAARILELGPMLERKPKQLSGGQRQR 141

Query: 144 VAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQVEAMTMG 203
           VA+GRAIVR P++FL DEPLSNLDA LRV  R ++A L + L  T +YVTHDQVEAMT+ 
Sbjct: 142 VAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELARLHKELQATMIYVTHDQVEAMTLA 201

Query: 204 DRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPIT-----------DGG 252
           D+V VL  G ++QV SP  +Y +PANLFVAGF+G+P M  ++  +T           D G
Sbjct: 202 DKVVVLNGGRIEQVGSPLELYHQPANLFVAGFLGTPKMGFLKGKVTRVERQNCEVLLDAG 261

Query: 253 VKFGNSVVPVNREALSAADKGDRTVTVGVRPEHFDVVELGGAVAASLSKDSADAPAGLAV 312
            +     +P++   LS        VT+G+RPEH ++   G                 L V
Sbjct: 262 TRI---TLPLSGANLSIGG----AVTLGIRPEHLNLALPGDCT--------------LQV 300

Query: 313 SVNVVEELGADGYVYGTAEVGGEVKDLVVRVNGRQVPEKGSTLHVVPRPGETHVFSTS 370
           + +V E LG+D + +     G   + L +R+ G      G  L +       H+F  +
Sbjct: 301 TADVSERLGSDTFCHVLTASG---EALTMRIRGDLASRYGEQLSLHLDAEHCHLFDAN 355


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: 391
Number of extensions: 18
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: 367
Length adjustment: 30
Effective length of query: 347
Effective length of database: 337
Effective search space:   116939
Effective search space used:   116939
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