GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Burkholderia phytofirmans PsJN

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 BPHYT_RS35680 BPHYT_RS35680 sugar ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>FitnessBrowser__BFirm:BPHYT_RS35680
          Length = 360

 Score =  302 bits (774), Expect = 8e-87
 Identities = 170/365 (46%), Positives = 230/365 (63%), Gaps = 26/365 (7%)

Query: 17  DKPAVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKD 76
           D   V  +D+ I+DGEF+VLVGPSGCGKST +RM+AGLE+++GG + IG      L P+ 
Sbjct: 15  DTQVVHGIDLDIDDGEFVVLVGPSGCGKSTLMRMVAGLEEISGGDLMIGGTRANSLAPQQ 74

Query: 77  RDIAMVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKAL 136
           R+I+MVFQ+YALYPH++V +N+ F  +I     A  + ++E AAK+L+L  YLDR P+AL
Sbjct: 75  RNISMVFQSYALYPHLSVYENIAFGPRIRKESSASFKPRIEAAAKMLNLGGYLDRLPRAL 134

Query: 137 SGGQRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQ 196
           SGGQRQRVAMGRA+VREP +FL DEPLSNLDAKLRV  RT+I +L +RL  T +YVTHDQ
Sbjct: 135 SGGQRQRVAMGRAVVREPSLFLFDEPLSNLDAKLRVQMRTEIKALHQRLKNTVIYVTHDQ 194

Query: 197 VEAMTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPITDGGVKFG 256
           +EAMTM DR+ V+  G ++Q+  P  +YD PANLFVA F+GSP+MN  E  I       G
Sbjct: 195 IEAMTMADRIVVMNAGRIEQIGRPLELYDHPANLFVASFLGSPSMNFAEGVIASRAQGQG 254

Query: 257 NSV-----VPVNREALSAADKGDRTVTVGVRPEHFDVVELGGAVAASLSKDSADAPAGLA 311
            ++       +  E   A+      VT+GVRPEH + +             + DA     
Sbjct: 255 LALNLTGGGEIVLEGAPASAVVGAKVTLGVRPEHIETM-----------TPTPDA----T 299

Query: 312 VSVNVVEELGADGYVYGTAEVGGEVKDLVVRVNGRQVPEKGSTLHVVPRPGE-THVFSTS 370
           + V VVE  GA+ ++YG  ++GG    +  R   +  P +  TL +   P E  H+F T 
Sbjct: 300 MEVEVVEPTGAETHLYG--KIGGSTWCVTTRQRSKIEPGQRVTLRL---PAEHIHLFDTE 354

Query: 371 TGERL 375
           +G RL
Sbjct: 355 SGRRL 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: 392
Number of extensions: 21
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: 360
Length adjustment: 30
Effective length of query: 347
Effective length of database: 330
Effective search space:   114510
Effective search space used:   114510
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