GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtB in Dinoroseobacter shibae DFL-12

Align CbtB, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate 3609627 Dshi_3010 binding-protein-dependent transport systems inner membrane component (RefSeq)

Query= TCDB::Q97VF8
         (333 letters)



>FitnessBrowser__Dino:3609627
          Length = 339

 Score =  191 bits (486), Expect = 2e-53
 Identities = 114/331 (34%), Positives = 176/331 (53%), Gaps = 4/331 (1%)

Query: 5   WLIRRLASVIIAIFVTIVISWALLEFSPYSPANYIMQFINPQDFAQKPELYASLIDYLNT 64
           +LI R  + ++ +F+   + W +  FSP  PA  ++  +     A       +++  L  
Sbjct: 8   YLINRTITFVLTVFIAATLIWLIPRFSPVDPAEIMLSRMAAGGGAVADS--EAILAQLRA 65

Query: 65  LRPHGNPLI-NAVNYIWNTLHGNLGFSIIS-NVPVAELIAVALPWTLFIVVTSILISFFL 122
                +PLI   + Y+ N L  NLG S  S   PV+ LIA ALPWTL +++ S++I+F +
Sbjct: 66  DFGLNDPLIVQYLKYMGNLLTFNLGISTASFPTPVSVLIAQALPWTLGLMILSVVITFVI 125

Query: 123 GIRLGQKLGYLRGTKTDSVATVSLSILRSVPIYIYAVLLIYILAFIYHIFPTGGAYSIHV 182
           G  LG  + + R  K   V   +  I  S+P  +  +LL+YI +      P  G+Y + V
Sbjct: 126 GNALGAFMVWERTPKIWKVVIPTFMIFTSIPPILSGLLLMYIFSITLRWLPLTGSYGLTV 185

Query: 183 TPGFNLPFIASVLYHAFLPILTLTIVNLVGWILQMRANTIYVLGEDFVNFAEISGVKKDI 242
            PG++  FI+SV+ H  LP L++ +V    W L MR   I V GED+VN A+  G+K   
Sbjct: 186 EPGWDWAFISSVIEHGTLPALSIIVVTFGFWTLGMRGLMISVQGEDYVNLAKAKGLKPRY 245

Query: 243 IEKKYIGKNAILPLYTSLIISIGFSFSGSVFVEQTFSYPGVGNLLINSITSNDYPTEMGV 302
           +  KY+ +NAILP  T+  + IG   SG + VE+ F Y G+G LL ++I   D+    GV
Sbjct: 246 VLYKYMVRNAILPQITAFALKIGLLVSGQILVERIFGYNGMGKLLYDAILDQDFAVIQGV 305

Query: 303 FIIIIVAVIVGNLIADLTYSFLDPRAKVGEE 333
             III+   +   + DL Y  +DPR ++ EE
Sbjct: 306 SYIIILMTALSVFLVDLIYPLIDPRIRLSEE 336


Lambda     K      H
   0.327    0.144    0.429 

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: 289
Number of extensions: 11
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: 333
Length of database: 339
Length adjustment: 28
Effective length of query: 305
Effective length of database: 311
Effective search space:    94855
Effective search space used:    94855
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 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