GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Burkholderia phytofirmans PsJN

Align D-gluconate TRAP transporter, periplasmic component (characterized)
to candidate BPHYT_RS35760 BPHYT_RS35760 ABC transporter substrate-binding protein

Query= reanno::psRCH2:GFF2082
         (338 letters)



>FitnessBrowser__BFirm:BPHYT_RS35760
          Length = 341

 Score =  162 bits (409), Expect = 1e-44
 Identities = 96/310 (30%), Positives = 157/310 (50%), Gaps = 1/310 (0%)

Query: 2   KRLLISTLAAALLGSTLSLGYAQAADDIRPRMIRFGYGLNEDSNQGRAAKLLAEEVAKAS 61
           +R L+   AA  +   L       A      + ++G  L         ++  A ++ +AS
Sbjct: 6   RRTLLRAAAAVPVAGALGFPAIVRAASGPEFVFKYGNNLPLTHPLNVRSQEAANQIKEAS 65

Query: 62  GGKLKVRTFASASLGSDDQMQNALIGGAQEMMVGSTATLVGISKEMAVWDTPFLFTDPRQ 121
            G++++R F +  LG D  M   +  G  EM   S   +  ++  +A+    F F+D  Q
Sbjct: 66  KGRMEIRIFPNNQLGGDTDMLAQVRSGGIEMFTPSALVVSTLAPSVAINAVGFAFSDYNQ 125

Query: 122 ADQVLDGPVGRQVMDKLEEKGLVGLV-YWENGFRNVTNSARPIEKLEDFNGVKLRVMPNP 180
               +DG +G  V   +++ GL      W+NGFR  T S  PI   +   G+K+RV  +P
Sbjct: 126 VWGAMDGKLGAYVRAAMQKAGLESFEKMWDNGFRQTTTSNGPITSAQTMRGLKIRVPVSP 185

Query: 181 VFIDTFKRMGANAVPLPFSELFTALETKAVDGQENPFNTILSSKFYEVQKYLSVTNHVYS 240
           + ID FK +GA+   L FSE++++L+T  VD QENP   +  +K YEVQKY S+TNH++ 
Sbjct: 186 LSIDMFKGLGASPTSLQFSEVYSSLQTHIVDAQENPLPIVQVAKLYEVQKYCSLTNHMWD 245

Query: 241 PWIVTVSKRWWDGLSATEQGILMEAAEKARDAEREDTRREASQALAALKERGMQINEVSP 300
            +   ++ R W  L    QGI  +A  ++   +RED R+    A+A L+ +G+ IN  +P
Sbjct: 246 GYWFVLNPRAWQRLPKDLQGIASDAFNQSALKQREDVRKLNDAAVADLQSKGLSINRPTP 305

Query: 301 DEIQRMREKA 310
           D  +    +A
Sbjct: 306 DTFRAALRQA 315


Lambda     K      H
   0.315    0.131    0.368 

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: 226
Number of extensions: 10
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: 338
Length of database: 341
Length adjustment: 28
Effective length of query: 310
Effective length of database: 313
Effective search space:    97030
Effective search space used:    97030
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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