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_009156492.1 SACMADRAFT_RS24195 5-dehydro-2-deoxygluconokinase

Query= SwissProt::Q704D0
         (325 letters)



>NCBI__GCF_000244955.1:WP_009156492.1
          Length = 311

 Score =  114 bits (286), Expect = 2e-30
 Identities = 91/290 (31%), Positives = 129/290 (44%), Gaps = 6/290 (2%)

Query: 36  PLRYVAYFEKHVAGSEANFCIAATMAGARCSLIARVGDDEFGRNIVEYLRGRGVDVSHVK 95
           PL  V  F K + G+  N  +AA   G R +++ +VG D FG  +   LR  GV   +V 
Sbjct: 23  PLAGVRSFAKSLGGTATNVAVAAARLGRRTAVLTKVGPDGFGTYVRSALREFGVSPDYVG 82

Query: 96  VDPGAPTGIYFVQRHFPVPGRSRLIYYRKGSAGS-RVGPDDVDSSLISSADA--VHSTGI 152
                 T + F       P    L++YR   A    +  DDV   ++ S     V  TG+
Sbjct: 83  TAEDLLTPVVFCA--LDPPEDPPLLFYRAPLAPDLTLTADDVPWDVVDSVPLLWVTGTGM 140

Query: 153 TLALSDSANRAVHKAFGEAKRRTFDTNIRPALWPDLAAARRAILDVLNYGVDVLVTDPDD 212
               S +  R + +    A     D + RP  WPD+  AR  I  +L++ V V V +  +
Sbjct: 141 CAEPSRTTQRELLRRRNRAGHTVLDLDYRPMFWPDMPTARTEIGWLLDH-VTVAVGNRAE 199

Query: 213 TQILLGVRDPEEAYRKYRELGVQTLVYKLGAEGAYVFWNGGSYFRDALKVAVEDPTGAGD 272
            ++ +G  DPEEA R+    GV+  + K G+ G  V    GS+      VAV    GAGD
Sbjct: 200 AEVAVGTSDPEEAARRMLARGVELALIKKGSAGVLVATRDGSWTVPPFPVAVVCGLGAGD 259

Query: 273 AVAGYFVALYLSGVDPRRALDLAVAASALVVGVRGDNEALPSPREAEELL 322
              G  V   LSG DP R    A AA A+V       +A+P+  E E  L
Sbjct: 260 GFGGALVHGLLSGWDPVRIARYANAAGAIVAARLACADAMPTREEIERTL 309


Lambda     K      H
   0.319    0.137    0.401 

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: 285
Number of extensions: 21
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: 325
Length of database: 311
Length adjustment: 27
Effective length of query: 298
Effective length of database: 284
Effective search space:    84632
Effective search space used:    84632
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 (21.7 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