GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Billgrantia desiderata SP1

Align D-gluconate TRAP transporter, periplasmic component (characterized)
to candidate WP_086509696.1 BZY95_RS09480 TRAP transporter substrate-binding protein

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



>NCBI__GCF_002151265.1:WP_086509696.1
          Length = 331

 Score =  214 bits (544), Expect = 3e-60
 Identities = 123/328 (37%), Positives = 190/328 (57%), Gaps = 8/328 (2%)

Query: 1   MKRLLISTLAAALLGSTLSL-GYAQAAD--DIRPRMIRFGYGLNEDSNQGRAAKLLAEEV 57
           MK    STLA   LG +L+L   AQA+D  D+ P  +R  + +NE      AA    E V
Sbjct: 1   MKIFARSTLA---LGISLALVSTAQASDFADMDPVTLRLAHVVNEQDGFHIAAVKFQELV 57

Query: 58  AKASGGKLKVRTFASASLGSDDQMQNALIGGAQEMMVGSTATLVGISKEMAVWDTPFLFT 117
           A+ + G + V  + +ASLG +  +   +  G  +M V +   +    +EMAV++ PFLF 
Sbjct: 58  AERTEGAVSVDIYPNASLGDERTLLEGMQIGTVDMGVITNGPVANFVEEMAVFELPFLFP 117

Query: 118 DPRQADQVLDGPVGRQVMDKLEEKGLVGLVYWENGFRNVTNSARPIEKLEDFNGVKLRVM 177
            P+ A +VLDGP+G++++DKL E  L GL Y E GFRN+TNS RP+   ED NG+++RVM
Sbjct: 118 SPQAAYEVLDGPIGQELLDKLAEVNLKGLAYAERGFRNLTNSERPVRSPEDLNGLRIRVM 177

Query: 178 PNPVFIDTFKRMGANAVPLPFSELFTALETKAVDGQENPFNTILSSKFYEVQKYLSVTNH 237
            NPV+ DTF+ +GANA+P+ ++E  TA++   +DGQENP N I S K +E Q +++++ H
Sbjct: 178 ENPVYTDTFRELGANAIPMAWTEALTAMQQGTIDGQENPVNVIHSFKLHETQDHMTLSRH 237

Query: 238 VYSPWIVTVSKRWWDGLSATEQGILMEAAEKARDAEREDTRREASQALAALKERGMQINE 297
            Y+P +  +    W+ L    Q +L++AA++A + ER       +  L  L+  GMQI  
Sbjct: 238 TYAPALFVMGMPAWNQLPEAAQEVLVQAAQEAAEHERRVNAEMEAGQLEELRAAGMQI-- 295

Query: 298 VSPDEIQRMREKAQPAIQTVIDAVGQEL 325
           V   +++  +   +P  +   D  G  L
Sbjct: 296 VDDADLEAFQAAVRPVYEKYGDQFGDYL 323


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: 208
Number of extensions: 14
Number of successful extensions: 1
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: 331
Length adjustment: 28
Effective length of query: 310
Effective length of database: 303
Effective search space:    93930
Effective search space used:    93930
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 Apr 09 2024. 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