GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Ruegeria conchae TW15

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_010442382.1 G7G_RS0115650 ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>NCBI__GCF_000192475.1:WP_010442382.1
          Length = 349

 Score =  305 bits (782), Expect = 1e-87
 Identities = 170/356 (47%), Positives = 224/356 (62%), Gaps = 26/356 (7%)

Query: 21  VDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKDRDIA 80
           VD  D+ I D EFLVL+GPSGCGK+T++RM+AGLED + G I I    V  + PKDRD+A
Sbjct: 19  VDNFDLTIADKEFLVLLGPSGCGKTTTMRMIAGLEDASEGDILIDGARVNDMEPKDRDVA 78

Query: 81  MVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKALSGGQ 140
           MVFQ+YALYP+M V +N+ F LK+ G+  A   +KV  A+ +++L  +L RKP  LSGGQ
Sbjct: 79  MVFQSYALYPNMNVYENIRFPLKVRGIDPATHDEKVRRASAMVELDDFLHRKPAELSGGQ 138

Query: 141 RQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQVEAM 200
           RQRVA+ RAIVREP VFLMDEPLSNLDAKLRVSTR QI +L   L +TT+YVTHDQ+EAM
Sbjct: 139 RQRVALARAIVREPNVFLMDEPLSNLDAKLRVSTRAQIKNLSHELAVTTIYVTHDQIEAM 198

Query: 201 TMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPITDGGVKFGNSVV 260
           T+ DRV ++K G++QQV SP ++YD+PAN FVA FIG+PAMNLV     DG VK G  V 
Sbjct: 199 TLADRVVIMKQGVVQQVGSPTDIYDEPANTFVASFIGNPAMNLV-----DGDVKGG--VF 251

Query: 261 PVNREALSAADKGDRTVTVGVRPEHFDVVELGGAVAASLSKDSADAPAGLAVSVNVVEEL 320
                 +   +  D  +T+G R E  +VVE GG + A +                  +EL
Sbjct: 252 RARNTEVQGLNAPDGPITLGFRAEDANVVESGGEINAPI----------------YTQEL 295

Query: 321 GADGYVYGTAEVGGEVKDLVVRVNGRQVPEKGSTLHVVPRPGETHVFSTSTGERLS 376
             D  +  +  +GG +  +      R   +   ++H+       H+F   TG RL+
Sbjct: 296 LGDSTMV-SVRIGGALVSVKADKTYRAEIDDQVSIHI--HTDHCHLFDAQTGARLN 348


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: 384
Number of extensions: 16
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: 349
Length adjustment: 29
Effective length of query: 348
Effective length of database: 320
Effective search space:   111360
Effective search space used:   111360
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.

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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