GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kdgK in Lactobacillus shenzhenensis LY-73

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_022529572.1 L248_RS07595 sugar kinase

Query= SwissProt::P50845
         (324 letters)



>NCBI__GCF_000469325.1:WP_022529572.1
          Length = 318

 Score =  225 bits (574), Expect = 1e-63
 Identities = 126/312 (40%), Positives = 186/312 (59%), Gaps = 5/312 (1%)

Query: 6   VTFGESMAMFYANEYG-GLHEVSTFSKGLAGAESNVACGLARLGFRMGWMSKVGNDQLGT 64
           +T GE +A+F + +    L +   F K LAGAE NVA G++RLG    +++++G D  G 
Sbjct: 5   LTIGEPIALFASEDMDKSLKDAVHFHKFLAGAEVNVAVGVSRLGHSAQYITRLGEDPFGD 64

Query: 65  FILQELKKEGVDVSRVIRSQDENPTGLLLKSKVKEGDPQVTYYRKNSAASTLTTAEYPRD 124
           FI  +L +  +     I S  +  T   LK +V  GDP + Y+R+NSAA+        + 
Sbjct: 65  FIKDQLAENQIGTD-YISSTPDYWTAFQLKDRVSHGDPSIFYFRRNSAAAHFEKRMLDKI 123

Query: 125 YFQCAGHLHVTGIPPALSAEMKDFTYHVMNDMRNAGKTISFDPNVRPSLWPDQATMVHTI 184
            F      H++GI PA+S +  D   +++  +       +FDPN+RP LW  Q  M  T+
Sbjct: 124 DFSGVKFAHLSGIFPAISDQALDAFKYLIQLLHEHNIRTTFDPNLRPQLWSSQEKMAGTL 183

Query: 185 NDLAGLADWFFPGIAEGELLTGEKTPEGIADYYLKKG--ASFVAIKLGKEGAYFKTGTSE 242
           N+LA  A+   PG  EG++L G   P+ IAD+YL +      V +K G +GAY +T   +
Sbjct: 184 NELAKEAEIILPGDNEGKILVGSDDPKAIADFYLGQSDRTQTVVVKTGAKGAYVQTKAGD 243

Query: 243 GF-LEGCRVDRVVDTVGAGDGFAVGVISGILDGLSYKDAVQRGNAIGALQVQAPGDMDGL 301
            + + G +VD+VVDTVGAGDGFA+G+++ +++G S +DAV R NA+GA  VQAPGD DG 
Sbjct: 244 SYTVPGFKVDQVVDTVGAGDGFALGLVTALMEGQSLRDAVIRANAVGAFAVQAPGDNDGY 303

Query: 302 PTREKLASFLSA 313
           PT EKLA+FL+A
Sbjct: 304 PTPEKLAAFLAA 315


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: 311
Number of extensions: 12
Number of successful extensions: 3
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 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