GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK in Phyllobacterium brassicacearum STM 196

Align PTS-dependent dihydroxyacetone kinase, dihydroxyacetone-binding subunit DhaK; EC 2.7.1.121 (characterized)
to candidate WP_106709791.1 CU102_RS04490 dihydroxyacetone kinase subunit DhaK

Query= SwissProt::Q9CIV8
         (332 letters)



>NCBI__GCF_003010955.1:WP_106709791.1
          Length = 338

 Score =  273 bits (698), Expect = 4e-78
 Identities = 143/313 (45%), Positives = 202/313 (64%), Gaps = 1/313 (0%)

Query: 4   EKIINQPQDVVSEMLDGLTYAYGDLIEKVPDFEIIQRKSPKSGKVALVSGGGSGHKPAHA 63
           +K +N+   +V+E L+G   A+G LI    + + ++R+    GKVA++SGGG+GH+P H 
Sbjct: 2   KKFMNEAAAMVAESLEGFVSAHGGLIMFGAERKFVRRRHLTPGKVAIISGGGAGHEPLHV 61

Query: 64  GFVGEGMLSAAVCGAIFTSPTPDQIYEAIKSADEGAGVLLIIKNYLGDVMNFEMAREMAE 123
           GFVG GML AA  G IFTSPTPDQI  AI+  D GAG LLI+KNY GDVMNFEMA E A 
Sbjct: 62  GFVGHGMLDAACTGHIFTSPTPDQIIAAIEETDTGAGCLLIVKNYAGDVMNFEMAAE-AV 120

Query: 124 MEEIKVEQIIVDDDIAVENSLYTQGRRGVAGTVLVHKILGAAAHQEASLDEIKDLADKVV 183
           +   ++E +IV DD+A + +  + GRRGVAGT++V KILGAAA    +L  +K L  ++ 
Sbjct: 121 LGRHRIETVIVSDDVAAQGAARSSGRRGVAGTLIVEKILGAAAEAGVNLAGLKALGGRME 180

Query: 184 KNIKTIGLALSAATVPEVGKPGFVLDDNEIEYGVGIHSEPGYRREKMKTSYELATELVGK 243
             I T+G+ALS  TVP+ G+  F L+ +E+E GVGIH EPG  R+K+  +  +A  +   
Sbjct: 181 TQIHTMGVALSGVTVPDTGRATFTLEPDEMEVGVGIHGEPGLYRQKIADADTIARLICST 240

Query: 244 LKEEFKFEAGQKYGILVNGMGATPLMEQFIFMNDVAKLLTEENIEILFKKVGNYMTSIDM 303
           +  +   + G +  +LVNG G TP  E ++  N   +L     I IL   VG Y+TS+DM
Sbjct: 241 ILADTGLQNGDRALLLVNGFGGTPTPELYLMYNVARRLFEASGIRILRSLVGTYVTSLDM 300

Query: 304 AGLSLTMIKLEDD 316
           AGLS+T+  L+++
Sbjct: 301 AGLSVTLSLLDEE 313


Lambda     K      H
   0.315    0.135    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: 304
Number of extensions: 11
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: 332
Length of database: 338
Length adjustment: 28
Effective length of query: 304
Effective length of database: 310
Effective search space:    94240
Effective search space used:    94240
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: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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