GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Teredinibacter turnerae T7901

Align glucokinase (EC 2.7.1.2) (characterized)
to candidate WP_015820092.1 TERTU_RS14805 fructokinase

Query= BRENDA::Q8RDE9
         (315 letters)



>NCBI__GCF_000023025.1:WP_015820092.1
          Length = 296

 Score =  108 bits (270), Expect = 2e-28
 Identities = 96/322 (29%), Positives = 146/322 (45%), Gaps = 56/322 (17%)

Query: 7   GVDLGGTK----ISTGIVDENGNIIKSIKIPTMAEKGPDVVIERIEESIYQVLKDTGLEM 62
           G++LGGTK    I TG+     +I   ++IPT     P   + +I   +           
Sbjct: 8   GIELGGTKTICLIGTGV----DSIRDQLQIPTT---NPADTLGQIHTFL--------ASQ 52

Query: 63  SNLKGIGIGSPGPLN-----AKKGIVISPPNLPHWSNVPIVEILSKRLGIEVRLENDANA 117
             L GIGIG+ GP+N     A  G + S P  P WS+  +V    +R    + L+ D NA
Sbjct: 53  GELAGIGIGAFGPVNIDPGSANYGCIESTPK-PGWSHTSVVPFFRERFSCPINLDTDVNA 111

Query: 118 AAIGEHLFGSGRGVDNFVYITVSTGIGGGVIIEGKLYSGENSNAAEIGHHTINFDGPRCN 177
           AAI EH  G+G+G+ NF+YITV TGIGGG +IEG    G  ++  E+GH  +    PR  
Sbjct: 112 AAIAEHQHGNGKGLRNFIYITVGTGIGGGALIEGAPVRG--NSHPEMGHIAL----PR-- 163

Query: 178 CGNYGCFEAYASGTAIARFAREGIEKGIKTKIKELAGEGEVKAEHVFEAAKLGDEFAKEL 237
              +   E + S     +   EG+  G   + +      E   EH               
Sbjct: 164 ---HMADETFLSACPYHQNCAEGLASGSALRKRWGMPLNEFPPEH-------------PA 207

Query: 238 VEKEAFYLGVGIANIMAFYNPRKIAIGGGVSAQW------DMLYEKMMETVRKKALKPNA 291
            + +A YL     ++   ++P++I +GGGVS++         LY+K+   V    L+ + 
Sbjct: 208 WDMQASYLAEFFHSLTLLFSPQRIIVGGGVSSEQLLARVRTALYKKLNGYVDALKLEASL 267

Query: 292 EVCEVVKAQLGENIGVLGAAAL 313
           E   +   +L  N G LG+  L
Sbjct: 268 E-SYLCLPELAGNAGPLGSLML 288


Lambda     K      H
   0.316    0.138    0.398 

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: 228
Number of extensions: 14
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: 315
Length of database: 296
Length adjustment: 27
Effective length of query: 288
Effective length of database: 269
Effective search space:    77472
Effective search space used:    77472
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: 48 (23.1 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