GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kdgK in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Align 2-dehydro-3-deoxygluconokinase; 2-keto-3-deoxygluconokinase; 3-deoxy-2-oxo-D-gluconate kinase; KDG kinase; EC 2.7.1.45 (characterized)
to candidate WP_068166855.1 HTA01S_RS01875 sugar kinase

Query= SwissProt::P50845
         (324 letters)



>NCBI__GCF_001592305.1:WP_068166855.1
          Length = 318

 Score =  295 bits (755), Expect = 1e-84
 Identities = 153/312 (49%), Positives = 208/312 (66%), Gaps = 2/312 (0%)

Query: 3   LDAVTFGESMAMFYANEYGGLHEVSTFSKGLAGAESNVACGLARLGFRMGWMSKVGNDQL 62
           LD +T GE+M +F A + G L + S+F++  AGAE NVA GLARLG R+G+++++G D  
Sbjct: 8   LDVITIGEAMVLFAAQQAGPLDDASSFARTTAGAELNVAIGLARLGLRVGYLTRLGQDLF 67

Query: 63  GTFILQELKKEGVDVSRVIRSQDENPTGLLLKSKVKEG-DPQVTYYRKNSAASTLTTAEY 121
           G  I   L +EG+D  +V+    E+PTG +LKS+  +G DPQ+ Y+RK SAAS +   E 
Sbjct: 68  GRHIAAVLSREGIDRQQVVMDA-EHPTGFMLKSRSDDGSDPQIQYFRKGSAASHMQVGEL 126

Query: 122 PRDYFQCAGHLHVTGIPPALSAEMKDFTYHVMNDMRNAGKTISFDPNVRPSLWPDQATMV 181
              Y   A HLH+TGI  A++   ++    +    R AG +ISFDPN+RP+LW  +  MV
Sbjct: 127 SSAYCASARHLHLTGIFVAVTPSTREVVLELAARSRAAGLSISFDPNLRPALWRSKDEMV 186

Query: 182 HTINDLAGLADWFFPGIAEGELLTGEKTPEGIADYYLKKGASFVAIKLGKEGAYFKTGTS 241
            ++N L+  +DW  PG+ EG LLTG  + +GIAD+YL++GA  V +KLG EGA++ T T 
Sbjct: 187 ASLNQLSTFSDWVLPGLEEGRLLTGRDSVQGIADFYLERGAQGVVVKLGPEGAFYATPTE 246

Query: 242 EGFLEGCRVDRVVDTVGAGDGFAVGVISGILDGLSYKDAVQRGNAIGALQVQAPGDMDGL 301
            G + G  V RV+DTVGAGDGFAVGVISG+L+GL+   A  RGNAIGA  VQ PGD DGL
Sbjct: 247 RGHVAGVPVTRVMDTVGAGDGFAVGVISGLLEGLTPAAAAARGNAIGARVVQFPGDADGL 306

Query: 302 PTREKLASFLSA 313
           PTR +L +   A
Sbjct: 307 PTRAELDALRKA 318


Lambda     K      H
   0.317    0.135    0.399 

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: 328
Number of extensions: 18
Number of successful extensions: 2
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: 324
Length of database: 318
Length adjustment: 28
Effective length of query: 296
Effective length of database: 290
Effective search space:    85840
Effective search space used:    85840
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 Apr 09 2024. 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