GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Dinoroseobacter shibae DFL-12

Align TM0028, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate 3607471 Dshi_0884 oligopeptide/dipeptide ABC transporter, ATPase subunit (RefSeq)

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Dino:3607471
          Length = 360

 Score =  193 bits (491), Expect = 5e-54
 Identities = 117/330 (35%), Positives = 179/330 (54%), Gaps = 13/330 (3%)

Query: 1   MKEILLKAENVRAYYKLEKVSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMV 60
           M + +L   N+          ++ VD +S++I   E++GVVGESG GK+   N +   + 
Sbjct: 1   MTQPVLSIRNLTVDIPTRYAVLRPVDKVSYDIAPGEILGVVGESGAGKSMAGNAVIGLLT 60

Query: 61  KPLTLVDGKIFLRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEKYVR 120
            P  +  G+++L  NG+ ++  +    E  R+  GK+I ++ Q  + +L P +R+   + 
Sbjct: 61  PPAHISSGEVWL--NGKRIDRLT---PEQMRRVRGKDIGMVFQDPLTSLNPLLRIGDQLT 115

Query: 121 HLAESH-GIDEEELLDKARRRFEEVGLDPLW--IKRYPFELSGGMRQRAVIAIATILNPS 177
               +H  I   E  ++A    EEVG+      +  YP E SGGMRQR VIA+A    PS
Sbjct: 116 ETMLAHLPISRAEAEERAVAALEEVGIPAARQRVNSYPHEFSGGMRQRVVIALALCAEPS 175

Query: 178 LLIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKI 237
           L+IADEPT+ALDV  Q  ++ +L ++ R+    +++ ITHD+  + + ADR+ +MYAG++
Sbjct: 176 LVIADEPTTALDVSVQAQIIALLKRLCRER-GTAVMLITHDMGVIAEAADRVAVMYAGRL 234

Query: 238 VEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFHPRC 297
            E  PV  +L  P HPYT GL  S  TP      + +  IPG+ P L   P GC F PRC
Sbjct: 235 AELGPVREVLTAPRHPYTFGLMGS--TPLASKGLKRLHQIPGSMPRLGRLPPGCAFSPRC 292

Query: 298 PHAMDVCKEKEPPLTEIEPGRRVACWLYME 327
           P A D C+    P+  I+     ACW  M+
Sbjct: 293 PRAQDKCRHDPGPV--IDADGAAACWFPMD 320


Lambda     K      H
   0.321    0.138    0.405 

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: 337
Number of extensions: 20
Number of successful extensions: 4
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: 330
Length of database: 360
Length adjustment: 29
Effective length of query: 301
Effective length of database: 331
Effective search space:    99631
Effective search space used:    99631
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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