GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK' in Phyllobacterium brassicacearum STM 196

Align Triokinase/FMN cyclase; Bifunctional ATP-dependent dihydroxyacetone kinase/FAD-AMP lyase (cyclizing); EC 2.7.1.28; EC 2.7.1.29; EC 4.6.1.15 (characterized)
to candidate WP_106709791.1 CU102_RS04490 dihydroxyacetone kinase subunit DhaK

Query= SwissProt::F1RKQ4
         (579 letters)



>NCBI__GCF_003010955.1:WP_106709791.1
          Length = 338

 Score =  222 bits (565), Expect = 2e-62
 Identities = 134/334 (40%), Positives = 194/334 (58%), Gaps = 11/334 (3%)

Query: 4   KKLVNSVAGCADDALAGLVACNPSLQLLQGHRVALRSDLDSLKGRVALLSGGGSGHEPAH 63
           KK +N  A    ++L G V+ +  L +    R  +R       G+VA++SGGG+GHEP H
Sbjct: 2   KKFMNEAAAMVAESLEGFVSAHGGLIMFGAERKFVRRR-HLTPGKVAIISGGGAGHEPLH 60

Query: 64  AGFIGKGMLTGVIAGAVFTSPAVGSILAAIRAVAQAGTVGTLLIVKNYTGDRLNFGLARE 123
            GF+G GML     G +FTSP    I+AAI         G LLIVKNY GD +NF +A E
Sbjct: 61  VGFVGHGMLDAACTGHIFTSPTPDQIIAAIEETDTGA--GCLLIVKNYAGDVMNFEMAAE 118

Query: 124 QARAEGIPVEMVVVGDD-SAFTVLKKAGRRGLCGTVLIHKVAGALAEAGVGLEEITNRVS 182
                   +E V+V DD +A    + +GRRG+ GT+++ K+ GA AEAGV L  +     
Sbjct: 119 AVLGRH-RIETVIVSDDVAAQGAARSSGRRGVAGTLIVEKILGAAAEAGVNLAGLKALGG 177

Query: 183 VVAKAMGTLGVSLSSCSVPGS-RPTFELSADEVELGLGIHGEAGVLRIKMATADEIVAHM 241
            +   + T+GV+LS  +VP + R TF L  DE+E+G+GIHGE G+ R K+A AD I    
Sbjct: 178 RMETQIHTMGVALSGVTVPDTGRATFTLEPDEMEVGVGIHGEPGLYRQKIADADTIA--- 234

Query: 242 LNHMTDSSNVSHVPVQSGSSVVLMVNNLGGLSYLELGIIADAAVRFLEGRGVKIARALVG 301
              +  S+ ++   +Q+G   +L+VN  GG    EL ++ + A R  E  G++I R+LVG
Sbjct: 235 --RLICSTILADTGLQNGDRALLLVNGFGGTPTPELYLMYNVARRLFEASGIRILRSLVG 292

Query: 302 TFMSALEMPGVSLTLLLVDEPLLKLIDAETTAAA 335
           T++++L+M G+S+TL L+DE  L L DA    AA
Sbjct: 293 TYVTSLDMAGLSVTLSLLDEEALHLWDAPVLTAA 326


Lambda     K      H
   0.315    0.131    0.367 

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: 449
Number of extensions: 24
Number of successful extensions: 4
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: 579
Length of database: 338
Length adjustment: 32
Effective length of query: 547
Effective length of database: 306
Effective search space:   167382
Effective search space used:   167382
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: 51 (24.3 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