GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kdgK in Saccharomonospora marina XMU15

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_009155646.1 SACMADRAFT_RS19930 sugar kinase

Query= SwissProt::Q53W83
         (309 letters)



>NCBI__GCF_000244955.1:WP_009155646.1
          Length = 314

 Score =  195 bits (495), Expect = 1e-54
 Identities = 129/312 (41%), Positives = 172/312 (55%), Gaps = 16/312 (5%)

Query: 4   VVTAGEPLVALVPQEPGHLRGKRLLEVYVGGAEVNVAVALARLGVKVGFVGRVGEDELGA 63
           +VT GE L A+   + G LR    ++V + G+E  VA+ +ARLGV   + GRVG DE GA
Sbjct: 6   LVTFGESL-AVFSTQSGKLRHAGSVDVGIAGSEAIVAIGVARLGVPASWAGRVGADEPGA 64

Query: 64  MVEERLRAEGVDLTHF---RRAPGFTGLYLREYLPLGQGRVFYYRKGSAGSALAPGAFDP 120
           +V  RLR EGVD +     + AP  TGL L+++      R  YYR GSAG+ L P     
Sbjct: 65  LVLLRLRDEGVDTSAAMTDQHAP--TGLMLKDFRTTDATRCAYYRNGSAGTRLCPEDIPE 122

Query: 121 DYLEGVRFLHLSGITPALSPEARAFSLWAMEEAKRRGVRVSLDVNYRQTLWSPEEARGFL 180
           D +     LHLSG+TP+LS  A    L A+E A+  GV VS DVNYR  LW P+EA G L
Sbjct: 123 DRIRQAGVLHLSGLTPSLSDTAAKAVLAAVEVAREEGVPVSFDVNYRNALWEPQEATGVL 182

Query: 181 ERALPGVDLLFLSEEEAELLFGRVEEALR---------ALSAPEVVLKRGAKGAWAFVDG 231
              +   D++F S +EA  L G   E +R          L   +V++K G +GA A + G
Sbjct: 183 LDLVSRADIVFASVDEAAPL-GFTGEPVRPEQLLAYLAELGPEQVIVKLGPRGALAELHG 241

Query: 232 RRVEGSAFAVEAVDPVGAGDAFAAGYLAGAVWGLPVEERLRLANLLGASVAASRGDHEGA 291
            R +   + V A+D  GA DAF AGYLA  + G P + R+R A    A   +  GD EG 
Sbjct: 242 CRYDVPTYPVRAIDSEGADDAFVAGYLADFLAGAPPDRRVRTAAACRAFAVSVHGDWEGL 301

Query: 292 PYREDLEVLLKA 303
           P RE+L+ L +A
Sbjct: 302 PDREELKQLARA 313


Lambda     K      H
   0.320    0.139    0.407 

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: 288
Number of extensions: 14
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: 309
Length of database: 314
Length adjustment: 27
Effective length of query: 282
Effective length of database: 287
Effective search space:    80934
Effective search space used:    80934
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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