GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK' in Sinorhizobium meliloti 1021

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 SM_b20312 SM_b20312 dihydroxyacetone kinase

Query= BRENDA::Q3LXA3
         (575 letters)



>FitnessBrowser__Smeli:SM_b20312
          Length = 695

 Score =  177 bits (448), Expect = 2e-48
 Identities = 111/327 (33%), Positives = 175/327 (53%), Gaps = 10/327 (3%)

Query: 4   KKLVNSVAGCADDALAGLVACNP-NLQLLQGHRVALRSDLDSLKGRVALLSGGGSGHEPA 62
           KK +N+     ++ L G V  +   LQ + G   AL +      G+V L+ GGG+GHEP 
Sbjct: 364 KKFLNNPNEVVEEMLDGAVKAHEIYLQPINGSHRALVARNGPRPGKVGLVIGGGTGHEPC 423

Query: 63  HAGFIGKGMLTGVIAGAVFTSPAVGSILAAIRAVAQAGTVGTLLIVKNYTGDRLNFGLAR 122
             G++GKG+   V  G +F+SP    I+    A A +G  G L +  NY GD +NF +A 
Sbjct: 424 FLGYVGKGLADAVAVGNIFSSPPPDPIVQC--AEAASGGEGVLFVYGNYAGDVMNFEMAA 481

Query: 123 EQARAEGIPVEMVVIGDDSAFT-VLKKAGRRGLCGTVLIHKVAGALAEAGVGLEEIAKQV 181
           E A  +GI V+ V+  DD A + V  + GRRG+ G   I K+AGA  + G+ LE      
Sbjct: 482 EIAEEKGIKVKTVLTTDDVASSPVEDREGRRGVAGNFFIFKIAGAACDRGLSLEACEAVT 541

Query: 182 NVVAKAMGTLGVSLSSCSVPGS-KPTFELSADEVELGLGIHGEAGVRRIKMATADEIVKL 240
                   T+GV+L   S+P + +  FE+  D++E+G+GIHGE GV R ++ +ADEI   
Sbjct: 542 RKANLRTYTVGVALEPGSMPQTRRHNFEIGPDDMEVGMGIHGEPGVTRERIRSADEITDS 601

Query: 241 MLDHMTNTTNASHVPVQPGSSVVMMVNNLGGLSFLELGIIADATVRSLEGRGVKIARALV 300
           ++D +        +   PG  V ++VN+ G    +EL I+     + L  + + I    +
Sbjct: 602 IMDRI-----FKEMKTAPGERVAVLVNSFGATPLMELYILFRRVQQRLAAKDILIEANWI 656

Query: 301 GTFMSALEMPGISLTLLLVDEPLLKLI 327
           G + ++L+M G S+T+L +D+ L  L+
Sbjct: 657 GHYCTSLDMAGASITILHLDQELSDLL 683


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: 833
Number of extensions: 51
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: 575
Length of database: 695
Length adjustment: 38
Effective length of query: 537
Effective length of database: 657
Effective search space:   352809
Effective search space used:   352809
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: 54 (25.4 bits)

This GapMind analysis is from Sep 17 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