GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Caldicellulosiruptor kronotskyensis 2002

Align Fructokinase; EC 2.7.1.4 (uncharacterized)
to candidate WP_013430999.1 CALKRO_RS10530 ROK family protein

Query= curated2:Q03417
         (301 letters)



>NCBI__GCF_000166775.1:WP_013430999.1
          Length = 316

 Score = 78.6 bits (192), Expect = 2e-19
 Identities = 90/321 (28%), Positives = 129/321 (40%), Gaps = 49/321 (15%)

Query: 11  IEGGGTKFMLALIDSDRKMLAVERVPTTTPE---ETLGKSVEFFKKALPQYA---DSFAS 64
           I+ GGT     ++D   K++    VPT       E +    E     + +     D   S
Sbjct: 6   IDLGGTNIAAGIVDEGGKIIKKGSVPTGAHRHYTEIMKDMAELSLNLVKECGLTLDDIHS 65

Query: 65  FGIASFGPLCLDRKSPKWGYITNTPKPFWPNTDVVTPFKEAFGCPVEIDTDVNGAALAEN 124
            GI S G    ++     G I  +    + N  +    ++    PV I+ D N AA  E 
Sbjct: 66  VGIGSPGAPDNEK-----GMILYSNNIAFLNVPMREEIQKYIPKPVNIENDANCAAYGEY 120

Query: 125 FWGASKGTHTSVYVTVGTGFGGGVLIDGKPIHGLAH--PEMGHGIPIRHPDDRDFEGCCP 182
             G +KGT  SV +T+GTG GGG++IDGK   G  H   E+GH +        D E C  
Sbjct: 121 IAGGAKGTKISVTITLGTGIGGGIIIDGKIFTGAHHAGAELGHMVIC-----VDGEQCTC 175

Query: 183 YHGGCYEGLASGTAIRKRWGKA--------LNEMEPAEFEKAREIIAF------------ 222
              GC+E  AS TA+ +   +A        + ++   +  K     AF            
Sbjct: 176 GRRGCWEAYASATALIRMTREAAARDINGTIMKLVNGDISKIDAKTAFDAKRMGDSTGAA 235

Query: 223 -------YLAHFNVTLQAFISPERIVFGGGV-MHVDGMLASVRRQTAEIANSYFEGADFE 274
                  YLA     +     PE I  GGGV    + +L  VR+   E    Y +     
Sbjct: 236 IVDRYVKYLAEGLANICNIFEPEVICIGGGVSKEGEYLLEPVRKLVYE--KFYCKQVPMP 293

Query: 275 KIIVLPGLGDQAGMMGAFALA 295
           KII    LG+ AG++GA  LA
Sbjct: 294 KIIPAV-LGNDAGIIGAALLA 313


Lambda     K      H
   0.320    0.139    0.435 

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: 208
Number of extensions: 10
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: 301
Length of database: 316
Length adjustment: 27
Effective length of query: 274
Effective length of database: 289
Effective search space:    79186
Effective search space used:    79186
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