GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dgoK in Paludibacter propionicigenes WB4

Align 2-dehydro-3-deoxygluconokinase (EC 2.7.1.45) (characterized)
to candidate WP_041620615.1 PALPR_RS02760 sugar kinase

Query= BRENDA::Q9WXS2
         (339 letters)



>NCBI__GCF_000183135.1:WP_041620615.1
          Length = 347

 Score =  303 bits (775), Expect = 5e-87
 Identities = 168/344 (48%), Positives = 225/344 (65%), Gaps = 6/344 (1%)

Query: 2   KVVTFGEIMLRLSPPDHKRIFQTDSFDVTYGGAEANVAAFLAQMGLDAYFVTKLPNNPLG 61
           K+VTFGEIMLRL+ P  +R  Q   F  T+GG EANVA  LA  G+   FVT+LP N + 
Sbjct: 4   KIVTFGEIMLRLATPGFERFSQATQFTATFGGGEANVAVSLANYGMKTEFVTRLPKNDIA 63

Query: 62  DAAAGHLRKFGVKTDYIARGGNRIGIYFLEIGASQRPSKVVYDRAHSAISEAKREDFDWE 121
           ++   +LRK+GV T+ I RGG+R+GIYFLE GA  R SKVVYDRA+S+I++ K    +W 
Sbjct: 64  ESCIMNLRKYGVGTNEILRGGDRVGIYFLETGAVARASKVVYDRANSSIADIKPGMVNWH 123

Query: 122 KILDGARWFHFSGITPPLGKELPLILEDALKVANEKGVTVSCDLNYRARLWT-KEEAQKV 180
           +I   A WFH++GITP L +       +A+++ANE GVTVS DLNYR  LW   + A +V
Sbjct: 124 EIFKDADWFHWTGITPALSQGAADACLEAIQIANEMGVTVSTDLNYRKNLWKYGKTASEV 183

Query: 181 MIPFMEYVDVLIANEEDIEKVLGISVEGLDL--KTGKLNREAYAKIAEEVTRKY-NFKTV 237
           M   +   D+++ NEED EKV GI  EG D+    G+++   +  +  ++ +K+   + V
Sbjct: 184 MPALVAGCDIILGNEEDAEKVFGIKPEGFDVAHTGGEVDAAEFESVCTQMMKKFPRAQKV 243

Query: 238 GITLRESISATVNYWSVMVFENGQPHFSNRYEI-HIVDRVGAGDSFAGALIYGSLMGFDS 296
            ITLR SI+A  N W  +++ NG  + S RY+I HIVDRVG GDSF G LIYG L   DS
Sbjct: 244 IITLRGSINANHNTWGGVLYSNGILYQSKRYDITHIVDRVGGGDSFMGGLIYGLLTYTDS 303

Query: 297 QKKA-EFAAAASCLKHTIPGDFVVLSIEEIEKLASGATSGRVER 339
            +KA EFA AASCLKHTI GD+ ++++ E+E L  G  SGRV R
Sbjct: 304 DQKALEFAVAASCLKHTIYGDYNLVTVAEVEGLMGGDGSGRVVR 347


Lambda     K      H
   0.319    0.136    0.397 

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: 336
Number of extensions: 18
Number of successful extensions: 5
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: 339
Length of database: 347
Length adjustment: 29
Effective length of query: 310
Effective length of database: 318
Effective search space:    98580
Effective search space used:    98580
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: 49 (23.5 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