GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1749 in Bacteroides thetaiotaomicron VPI-5482

Align TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate 351279 BT1751 Glycine betaine transport ATP-binding protein (NCBI ptt file)

Query= TCDB::Q9X271
         (324 letters)



>FitnessBrowser__Btheta:351279
          Length = 408

 Score =  137 bits (346), Expect = 3e-37
 Identities = 91/255 (35%), Positives = 143/255 (56%), Gaps = 18/255 (7%)

Query: 2   MELLNVNNLKVEFHRVEGIVKAVDGISYKLNKGESLGIVGESGSGKSVSVLSLLRLINRN 61
           +++L     K E  +  G   AV   +  +N+GE   I+G SGSGKS    +LLR INR 
Sbjct: 21  LKMLKEGKTKSEILKATGCTVAVKDANLSINEGEIFVIMGLSGSGKS----TLLRCINRL 76

Query: 62  GRIVDGEAIFLGKDLLKLNKEELRNIRGKDISIIFQN----PMTSLNPIIRVGIQVMEPI 117
            R   GE I  G D+ K++ +EL  IR K+++++FQN    P  S+   I  G+++    
Sbjct: 77  IRPTSGEVIINGTDIAKVSDKELLQIRRKELAMVFQNFGLLPHRSVLHNIAFGLELQG-- 134

Query: 118 IWHRLMKNEEARERAIELLERVGIPESPKRFLNYPFQFSGGMRQRVMIAMALACHPKLLI 177
                +K  E  ++A+E ++ VG+     + ++   + SGGM+QRV +A ALA +P++L+
Sbjct: 135 -----VKKGEREQKAMESMQLVGLKGYENQMVS---ELSGGMQQRVGLARALANNPEVLL 186

Query: 178 ADEPTTALDVTIQAQIMELLQELKEEYGMSVIFITHDLSVATNFCDRIITMYAGKIVEEA 237
            DE  +ALD  I+ Q+ + L  L+ +   +++FITHDLS A    DRI  M  G+IV+  
Sbjct: 187 MDEAFSALDPLIRVQMQDELLTLQSKMKKTIVFITHDLSEAIKLGDRIAIMKDGEIVQIG 246

Query: 238 PVEEILKTPLHPYTK 252
             EEIL  P + Y +
Sbjct: 247 TSEEILTEPANAYVE 261



 Score = 25.0 bits (53), Expect = 0.003
 Identities = 12/28 (42%), Positives = 19/28 (67%), Gaps = 4/28 (14%)

Query: 64  IVDGEAIFLGK----DLLKLNKEELRNI 87
           +VD   + +G+    DLLKL KE++R+I
Sbjct: 310 VVDSNNLLVGEVRLNDLLKLRKEQIRSI 337


Lambda     K      H
   0.320    0.139    0.401 

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: 280
Number of extensions: 17
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 324
Length of database: 408
Length adjustment: 29
Effective length of query: 295
Effective length of database: 379
Effective search space:   111805
Effective search space used:   111805
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.

Links

Downloads

Related tools

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