GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Erythrobacter gangjinensis K7-2

Align Solute-binding protein Bamb_6123 (characterized)
to candidate WP_047006206.1 AAW01_RS05310 TRAP transporter substrate-binding protein

Query= SwissProt::Q0B2F6
         (328 letters)



>NCBI__GCF_001010925.1:WP_047006206.1
          Length = 331

 Score =  290 bits (743), Expect = 3e-83
 Identities = 147/315 (46%), Positives = 200/315 (63%), Gaps = 4/315 (1%)

Query: 13  AVALMAGFAMSAQARVFRSADVHGDSFPTNMAVKFMGDELSKLTGGKDSIKVFGNSALGS 72
           A A++A    S  AR+ R+ D H D +PT  AVK MG+ L++ +GG+ +I+ +    LG 
Sbjct: 15  AGAMLAAGCASRDARLLRAVDTHPDGYPTVEAVKHMGELLAQRSGGRLAIEHYAGGVLGQ 74

Query: 73  EKDTVDQVRIGAIDMARVNGASFNEIVPESLIPSFPFLFRDVDHFRKAMYGPAGQKILDA 132
           E+D ++    G ID+ RVN A  N IVPE+++P  PFLF    H R AM G  G++ILDA
Sbjct: 75  ERDALEITIFGGIDLNRVNLAPLNPIVPETVVPGLPFLFSSTQHMRSAMDGEPGRRILDA 134

Query: 133 FAAKGMIALTFYESGARSIYA-KRPVRTPADMKGLKVRVQPSDLMVDEIRAMGGTPTPMP 191
               G+I L FY+SG RS Y  +R +  P D+ GLK+RVQ SDL V+ + A+GG PTPM 
Sbjct: 135 LEPHGLIGLCFYDSGGRSFYTTERLIEEPEDLAGLKIRVQSSDLFVEMVSALGGNPTPMD 194

Query: 192 FAEVYTGLKTGLVDAAENNLPSYEETKHFEVAPDYSETQHAMTPEVLVFSKKIWDTLSPQ 251
           F EVY GL  G VD AENN PSYE T+HFEVAP YSET+H M PE+L  S   WD LS  
Sbjct: 195 FGEVYQGLMQGTVDGAENNWPSYESTRHFEVAPYYSETRHVMAPEILTMSAISWDRLSED 254

Query: 252 EQAAIRKAAADSVPYYQKLWTAREASAQQAVTKGGANILPAAQVDRAAFVKAMQPLWTKY 311
           ++A IR+ A DSVPY + LW A+   ++ AV   G  +   A  + +AF + +QP+W ++
Sbjct: 255 DRALIRQCAQDSVPYMRGLWDAKVEQSRAAVVASGVRV---ANPEISAFQQRVQPVWDRF 311

Query: 312 EKTPQMKQIVDEIEA 326
             TP M+ +V +I+A
Sbjct: 312 VATPDMRALVADIQA 326


Lambda     K      H
   0.318    0.131    0.375 

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: 287
Number of extensions: 14
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: 328
Length of database: 331
Length adjustment: 28
Effective length of query: 300
Effective length of database: 303
Effective search space:    90900
Effective search space used:    90900
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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