GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Desulfacinum infernum DSM 9756

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_143156467.1 BUB04_RS12175 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_900129305.1:WP_143156467.1
          Length = 326

 Score =  309 bits (792), Expect = 5e-89
 Identities = 162/321 (50%), Positives = 223/321 (69%), Gaps = 6/321 (1%)

Query: 4   KVFITRQIPENGI-KMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKELL 62
           KV +T ++P+  + K+I    +++   + +   R  LL +V   + L+  +TD++D+E+ 
Sbjct: 2   KVLVTAKLPDEAVRKLILAGCDVDGHGEVRPMNREELLARVEGAEGLLCTITDRIDREVF 61

Query: 63  ENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEA 122
           + AP L++ A Y VG+D+ID+ EA +RGI VTNTP VLTDATADLAFAL+LAVARR+VE 
Sbjct: 62  DKAPGLRVAANYGVGFDHIDVAEAGRRGILVTNTPDVLTDATADLAFALILAVARRVVEG 121

Query: 123 DAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYSRT 182
           D   RSG+++     W PL FLG  + GKTLGIVGFGRIG+A+A+RA+GF M+++Y +R 
Sbjct: 122 DRRTRSGQFRF----WAPLHFLGTEVSGKTLGIVGFGRIGKAVARRARGFDMQVLYTARK 177

Query: 183 RKPEAEEE-IGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTSR 241
              + EEE +G  +   E LL +SDF+SLHVPLT +T H+IG +EL LMKP+A LINT+R
Sbjct: 178 PLEKREEERLGVRFAPLEELLAQSDFVSLHVPLTPQTRHLIGARELSLMKPSAFLINTAR 237

Query: 242 GAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREGMA 301
           G VVD  AL++ L+ G I GAGLDV+E EP     L  L+NVVL PH+GSAT E R  MA
Sbjct: 238 GPVVDEKALVETLRGGGIRGAGLDVYENEPELTPGLADLQNVVLLPHVGSATVETRTRMA 297

Query: 302 ELVAKNLIAFAKGEIPPNLVN 322
           E+  +NL+    G  PP+ +N
Sbjct: 298 EMAVENLLEGLAGRRPPHCLN 318


Lambda     K      H
   0.317    0.137    0.392 

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: 295
Number of extensions: 13
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: 331
Length of database: 326
Length adjustment: 28
Effective length of query: 303
Effective length of database: 298
Effective search space:    90294
Effective search space used:    90294
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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