GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Pedobacter sp. GW460-11-11-14-LB5

Align glucokinase (EC 2.7.1.2) (characterized)
to candidate CA265_RS11300 CA265_RS11300 sugar kinase

Query= BRENDA::Q8RDE9
         (315 letters)



>FitnessBrowser__Pedo557:CA265_RS11300
          Length = 313

 Score =  166 bits (419), Expect = 9e-46
 Identities = 101/313 (32%), Positives = 163/313 (52%), Gaps = 18/313 (5%)

Query: 2   KKFLCGVDLGGTKISTGIVDENGNIIKSIKIPTMAEKGPDVVIERIEESIYQVLKDTGLE 61
           + +  G+D+GG+ +  G+V++NG I+ SI +     K    +I  I E+I+   K     
Sbjct: 3   QSYAIGIDVGGSSLKCGVVNQNGEILYSIIVSLKNAKTQGAIIALIVEAIHTCAKKF--- 59

Query: 62  MSNLKGIGIGSPGPLNAKKGIVISPPNLPHWSNVPIVEILSKRLGIEVRLENDANAAAIG 121
            + + G+GIG PG +   K I+    NLP +  + + EIL +     + ++NDAN   +G
Sbjct: 60  KNPILGVGIGFPGIIYNNK-IIAGADNLPGFKQLALGEILQEVTRYNIVMDNDANLMGLG 118

Query: 122 EHLFGSGRGVDNFVYITVSTGIGGGVIIEGKLYSGENSNAAEIGHHTINFDGPRCNCGNY 181
           E  +G+ +   + V++TV TGIGG V+I+ KLY G  +   E+GH  +  +G  C CG  
Sbjct: 119 EMTYGAAKDCSDVVFLTVGTGIGGAVMIDNKLYGGFRNRGTELGHIVVQHNGLACACGGR 178

Query: 182 GCFEAYASGTAIARFAREGIEKGIKTKIKELAGEGEVKAEHVFEAAKLGDEFAKELVEKE 241
           GC EAYAS TA+         + I     E     E+  +++ E     +E+A E +E  
Sbjct: 179 GCLEAYASVTALLNH-----YQSIHPNPPE-----EIDGKYMVEKYLAREEYAVEAMESH 228

Query: 242 AFYLGVGIANIMAFYNPRKIAIGGGVSAQWDMLYEKMMETVRKKA--LKPNAEVCEVVKA 299
             YL  GI + +  ++P+KI IGGG+S        ++   ++  A  + P  E+  VV A
Sbjct: 229 FDYLATGIISFVNVFSPQKIVIGGGISESGAFYVREIERRIKTLAVPIAPGNEL--VVAA 286

Query: 300 QLGENIGVLGAAA 312
           +LG   G+LG AA
Sbjct: 287 RLGNKAGLLGCAA 299


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: 270
Number of extensions: 15
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: 313
Length adjustment: 27
Effective length of query: 288
Effective length of database: 286
Effective search space:    82368
Effective search space used:    82368
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 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