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_068167854.1 HTA01S_RS06210 5-dehydro-2-deoxygluconokinase

Query= SwissProt::P50845
         (324 letters)



>NCBI__GCF_001592305.1:WP_068167854.1
          Length = 651

 Score = 95.9 bits (237), Expect = 2e-24
 Identities = 89/337 (26%), Positives = 146/337 (43%), Gaps = 32/337 (9%)

Query: 4   DAVTFGESMAMFYANEYGG-LHEVSTFSKGLAGAESNVACGLARLGFRMGWMSKVGNDQL 62
           D    G      YA ++G  L +  + +  L G+ +N+A G+ARLG R   +S+VGN+Q+
Sbjct: 13  DLACLGRLAVDLYAQQFGSRLEDARSLAMYLGGSSANLAFGVARLGCRSAMVSRVGNEQM 72

Query: 63  GTFILQELKKEGVDVSRVIRSQDENPTGLLLKSKVKEGDPQVTYYRKNSAASTLTTAEYP 122
           G F+L+ L+ EG DVS+V          +LL  K ++  P + + R+N A   +  +   
Sbjct: 73  GRFLLERLQAEGCDVSQVQIDLQRLTALVLLGIKDRDTFP-LLFVRENCADMAIDASAIS 131

Query: 123 RDYFQCAGHLHVTGIPPALSAE-MKDFTYHVMNDMRNAGKTISFDPNVRPSLW------- 174
            D+      L +TG    LS E  +   +  +   R  G     D + RP LW       
Sbjct: 132 EDFIAQCRALAITG--THLSTEGTRAAAHKALQAARRHGTVTVLDIDYRPVLWGLTSRGA 189

Query: 175 -----PDQATMVHTINDLAGLAD--------WFFPGIAEGELLTGEKTPEGI---ADYYL 218
                   A +   + +   L D        +F  G    +L+   +    +   A   +
Sbjct: 190 GENRYVADAGVTRQLQESLPLFDLLVGTEEEFFIAGGVADDLIASLRAVRALCPQATLVV 249

Query: 219 KKGASFVAIKLGKEGAYFKTGTSEGFLEGCRVDRVVDTVGAGDGFAVGVISGILDGLSYK 278
           K+GA    +    EGA      +     G RV+ V++ +GAGD F  G+++ +L G  + 
Sbjct: 250 KRGALGCCV---IEGAVPDHIDAAPTYRGERVE-VLNVLGAGDAFLSGLMASLLQGKDWA 305

Query: 279 DAVQRGNAIGALQVQAPGDMDGLPTREKLASFLSAQR 315
           +A Q  NA GA+ V        +PT  +LA +    R
Sbjct: 306 EATQVANACGAIVVSRHACSAAMPTPAELAHWFGGSR 342


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: 434
Number of extensions: 21
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 324
Length of database: 651
Length adjustment: 33
Effective length of query: 291
Effective length of database: 618
Effective search space:   179838
Effective search space used:   179838
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 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