GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Phaeacidiphilus oryzae TH49

Align Fructokinase-1; Fructokinase I; OsFKI; EC 2.7.1.4 (characterized)
to candidate WP_084703970.1 BS73_RS11395 5-dehydro-2-deoxygluconokinase

Query= SwissProt::A2WXV8
         (323 letters)



>NCBI__GCF_000744815.1:WP_084703970.1
          Length = 385

 Score =  115 bits (288), Expect = 2e-30
 Identities = 100/328 (30%), Positives = 143/328 (43%), Gaps = 27/328 (8%)

Query: 8   VVSFGEMLIDFVPTVAGVSLAEAPAFVKAPGGAPANVAIAVARLGGGAAFVGKLGDDEFG 67
           +++ G + +D  P   GV LAE   F K  GG+  NVA+A ARL   +A V + G D FG
Sbjct: 22  LITMGRIGVDIYPLQIGVPLAEVETFGKFLGGSATNVAVAAARLRRRSAVVSRTGADPFG 81

Query: 68  RMLAAILRDNGVDDGGVVFDAGARTALAFVTLRADGEREFMFYRNPSADMLLTH-AELNV 126
             +   LR+ GVDD  V       T + F  +    +    FYR P A  L  H  EL++
Sbjct: 82  EYVHRALREFGVDDRWVTPVQRYPTPVTFCEIFPPDDFPIWFYRRPKAPDLEIHPEELDL 141

Query: 127 ELIKRAAVFHYGSISLIAEPCRSAHLRAM--EIAKEAGALLSYDPNLREALW-------- 176
           + I+ A +F      L  EP R+A L A+    A+       +D + R A W        
Sbjct: 142 DAIRSAGIFWITGTGLCEEPSRTATLAALAARSARPGAGPTVFDLDWRPAFWGGEGGASG 201

Query: 177 -------PSREEARTKILSIWDHADIVKVSEVELEFLTGIDSVEDDVVMKLWRPTMKLLL 229
                   +  EAR        HA +   +  E E  TG+   +      L     +L +
Sbjct: 202 DGGEGGARAMAEARPIYREALAHATVAVGNLDEAEVATGLRDPQ-ACAEALLELGAELAV 260

Query: 230 VTLGDQGCKYYARD-FRGAVPSYKVQQVDTTGAGDAFVGALLRRIVQDPSSLQDQKKLEE 288
           V  G +G     RD  R  VP   V+ V+  GAGDAF GAL   ++           LE 
Sbjct: 261 VKQGPKGVLALHRDGTRAQVPPVPVEVVNGLGAGDAFGGALCHGLLAG-------WPLER 313

Query: 289 AIKFANACGAITATKKGAIPSLPTEVEV 316
            +++ANA GAI A +     ++PT  E+
Sbjct: 314 TVRWANAAGAIVAGRLACSSAMPTPEEI 341


Lambda     K      H
   0.320    0.136    0.389 

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: 331
Number of extensions: 25
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: 323
Length of database: 385
Length adjustment: 29
Effective length of query: 294
Effective length of database: 356
Effective search space:   104664
Effective search space used:   104664
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 Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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