GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Burkholderia phytofirmans PsJN

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate BPHYT_RS29175 BPHYT_RS29175 ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__BFirm:BPHYT_RS29175
          Length = 390

 Score =  366 bits (939), Expect = e-106
 Identities = 193/359 (53%), Positives = 249/359 (69%), Gaps = 4/359 (1%)

Query: 3   SVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFI 62
           +V+VR+L++  GA TV++ L+LD+  GEF+VLLG SGCGKSTLL+ IAGL+DV+DG I I
Sbjct: 36  NVAVRNLTIQLGANTVIENLDLDVQAGEFVVLLGPSGCGKSTLLHSIAGLIDVTDGSIEI 95

Query: 63  KDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEILQ 122
              ++TW +PKDR I +VFQSYALYP M+VE+NLSF L++   P AEI +RV RASE+LQ
Sbjct: 96  AGEDMTWADPKDRRIALVFQSYALYPTMSVERNLSFALRINGTPKAEIARRVARASEMLQ 155

Query: 123 IQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLHQS 182
           + PLLKRKP++LSGGQRQRVAIGRA+VR+ DVFLFDEPLSNLDAKLR+ELR E+K+LHQ 
Sbjct: 156 LGPLLKRKPAQLSGGQRQRVAIGRAIVREADVFLFDEPLSNLDAKLRTELRRELKQLHQR 215

Query: 183 LKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMNFF 242
           L  TMIYVTHDQ+EA+TLA R+AVM+ GVIQQ   P  +Y  P+NLFVA F+G+P+MN  
Sbjct: 216 LGATMIYVTHDQVEAMTLATRMAVMRGGVIQQFGTPAEVYARPDNLFVATFLGTPAMNLI 275

Query: 243 RGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGEPTHQA 302
           +G +E +DG           DV+ YP  T    G   VLG+R E V++ E      +  A
Sbjct: 276 KGRLETRDGALHFCTEHWRLDVSRYPFRTTPANGLPCVLGVRAEDVRLAEG----ASEHA 331

Query: 303 VVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASIFDAESENRL 361
            V + EPMG   ++WL + G  ++     +     G     SFD    S+FD     RL
Sbjct: 332 KVSLVEPMGNHRVIWLDYHGVQVASIDQTKTPLAIGDAAAFSFDSTHVSLFDEAGGARL 390


Lambda     K      H
   0.320    0.137    0.392 

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: 412
Number of extensions: 18
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: 361
Length of database: 390
Length adjustment: 30
Effective length of query: 331
Effective length of database: 360
Effective search space:   119160
Effective search space used:   119160
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: 50 (23.9 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