GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK' in Klebsiella michiganensis M5al

Align triokinase (EC 2.7.1.28); glycerone kinase (EC 2.7.1.29); FAD-AMP lyase (cyclizing) (EC 4.6.1.15) (characterized)
to candidate BWI76_RS24595 BWI76_RS24595 dihydroxyacetone kinase subunit DhaK

Query= BRENDA::Q3LXA3
         (575 letters)



>FitnessBrowser__Koxy:BWI76_RS24595
          Length = 356

 Score =  226 bits (577), Expect = 9e-64
 Identities = 144/356 (40%), Positives = 194/356 (54%), Gaps = 26/356 (7%)

Query: 4   KKLVNSVAGCADDALAGLVACNPNLQLLQGHRVALRSDLDSLKGRVALLSGGGSGHEPAH 63
           KKL+N V     + LAGL   +P L+L Q      R+D   + G+VALLSGGGSGHEP H
Sbjct: 2   KKLINRVEDVLSEQLAGLAKAHPELRLHQDPVYVTRADAP-VAGKVALLSGGGSGHEPMH 60

Query: 64  AGFIGKGMLTGVIAGAVFTSPAVGSILAAIRAVAQAGTVGTLLIVKNYTGDRLNFGLARE 123
            G+IG+GML+G   G +FTSP    +     A+   G  G LLI+KNYTGD LNF  A E
Sbjct: 61  CGYIGQGMLSGACPGEIFTSPTPDKMFEC--AMNIDGGEGVLLIIKNYTGDILNFETATE 118

Query: 124 QARAEGIPVEMVVIGDDSAF-TVLKKAGRRGLCGTVLIHKVAGALAEAGVGLEEIAKQVN 182
                G+ V  VV+ DD A    L  AGRRG+  TVLI K+ GA AE G  LE  A+   
Sbjct: 119 LLHESGVKVTTVVVDDDVAVKDSLYTAGRRGVANTVLIEKLVGAAAERGDSLESCAELGR 178

Query: 183 VVAKAMGTLGVSLSSCSVPGS-KPTFELSADEVELGLGIHGEAGVRRIKMATADEIVKLM 241
            +     ++G++L +C+VP + +P+FEL  DE+E G+GIHGE G+ R +  + D  V  M
Sbjct: 179 KLNNLGHSIGIALGACTVPAAGQPSFELQDDEMEFGVGIHGEPGIDRRRFTSLDRTVDEM 238

Query: 242 LD-------------HMTNTTNA------SHVPVQPGSSVVMMVNNLGGLSFLELGIIAD 282
            D             H  N   A      +   +Q G  V+ +VNNLG     EL  + +
Sbjct: 239 FDTLLENGAYSRTLRHWDNVKGAWQEVAQTKQALQKGDRVIALVNNLGATPLSELYGVYN 298

Query: 283 ATVRSLEGRGVKIARALVGTFMSALEMPGISLTLLLVDEPLLKLIDA--ETTAAAW 336
              +  E  G+ I R L+G++ ++L+M G S+TLL VD+  L L DA   T A  W
Sbjct: 299 RLTQRCEETGIVIERNLIGSYCTSLDMVGFSITLLKVDDETLALWDAPVHTPALNW 354


Lambda     K      H
   0.315    0.130    0.365 

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: 462
Number of extensions: 16
Number of successful extensions: 6
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: 575
Length of database: 356
Length adjustment: 33
Effective length of query: 542
Effective length of database: 323
Effective search space:   175066
Effective search space used:   175066
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 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