GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Burkholderia phytofirmans PsJN

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate BPHYT_RS27960 BPHYT_RS27960 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>FitnessBrowser__BFirm:BPHYT_RS27960
          Length = 367

 Score =  213 bits (542), Expect = 6e-60
 Identities = 125/324 (38%), Positives = 186/324 (57%), Gaps = 14/324 (4%)

Query: 34  GGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRASPQERNIAQVFQFPVIYD 93
           G    LLGPSGCGKTT L +++GL +P+ G++  DG DVT    ++R+IA VFQ   +Y 
Sbjct: 29  GRFVVLLGPSGCGKTTTLRMIAGLELPTSGQIFIDGEDVTALRARQRDIAFVFQMFALYP 88

Query: 94  TMTVAENLAFPLRNRKVPEGQIKQRVGVIAEMLEMSGQLNQRAAGLAADAKQKISLGRGL 153
            MTV  N+AFPL+N  V   +I  RV   A ML +   L+++  GL+   +Q+++LGR +
Sbjct: 89  HMTVRNNIAFPLKNEHVSRKEIAARVAAAAHMLRIENILDRKTGGLSGGDRQRVALGRAI 148

Query: 154 VRADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHELKLTLIYVTHDQVEALTFADQVVVM 213
           VR    A L DEPL  +D   +  +  +L+++H+ L  T +YVTHDQ EA+  AD +VVM
Sbjct: 149 VR-QPKAFLMDEPLGTLDADFRELMCLELRKLHNALAATTVYVTHDQSEAMAMADDIVVM 207

Query: 214 TRGKAVQVGSADALFERPAHTFVGHFIGSPGMNFLPAHRDG------ENLSVAGHRLASP 267
            +G+ +Q G    ++  PA  FVG+FIGSP MNFLP   DG      E + + G +++ P
Sbjct: 208 NKGELLQAGPPQEIYHFPATVFVGNFIGSPPMNFLPV--DGGVDAGQEEVHLHGAQISVP 265

Query: 268 VGRALPAGALQVGIRPEYLALAQPQQAGALPGTVVQVQDIGTYQMLTAKVGEHTVKARFT 327
              A  A  + +GIRPE++ +    Q G L G V+  + +G++Q+L  +     V+ R  
Sbjct: 266 RCEA-AAERVLLGIRPEHVTI---NQHGPLRGKVIADEYLGSHQVLVVETALGVVRVRVG 321

Query: 328 PETRLPSSGDTAWLQVLGEHTCYY 351
            +  LP +G    L    E T  Y
Sbjct: 322 KDEGLP-AGSPVGLSFRKERTLLY 344


Lambda     K      H
   0.320    0.136    0.395 

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: 339
Number of extensions: 15
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: 358
Length of database: 367
Length adjustment: 29
Effective length of query: 329
Effective length of database: 338
Effective search space:   111202
Effective search space used:   111202
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