GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Chryseobacterium viscerum 687B-08

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_103234120.1 C1634_RS11965 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_002899945.2:WP_103234120.1
          Length = 328

 Score =  235 bits (600), Expect = 1e-66
 Identities = 141/325 (43%), Positives = 196/325 (60%), Gaps = 7/325 (2%)

Query: 4   KVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTD-KVDKELL 62
           KVFI ++IPE GIKM+E+     +  + +       L   +  D ++ +  D K DK+  
Sbjct: 2   KVFINKRIPETGIKMLEEAGLEIILPENENLSYEEWLGYCKNTDTILNVGGDFKYDKKFF 61

Query: 63  ENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEA 122
           +  P +K IA Y+VG+D+++I+EAT+R I + NTP VL+ AT+D+AF L+ +VARR    
Sbjct: 62  DACPNVKAIALYSVGFDHVEIKEATQRHIPIGNTPDVLSRATSDVAFLLMQSVARRASYN 121

Query: 123 DAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAK-GFGMKIIYYSR 181
              V+ G W      + PL  LG  L GKTLGI G GRIG  +A+++K  FGM IIY++R
Sbjct: 122 FQKVKDGNWN----AFDPLHALGQELYGKTLGIFGLGRIGYEMAEKSKKAFGMNIIYHNR 177

Query: 182 TRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTSR 241
               EAE E+GA YV FE L+K SD +S+H   T E   +      + MKP++I INT+R
Sbjct: 178 NHNEEAERELGAAYVSFEELIKNSDVLSVHANFTPEHKEVFNYSLFEQMKPDSIFINTAR 237

Query: 242 GAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEE-LFKLKNVVLAPHIGSATHEAREGM 300
           G   +   L +AL +  I GAGLDV   EP  +++ +  L +V + PHIGSAT EAR GM
Sbjct: 238 GGFHNQKDLYQALVDKKIWGAGLDVTNPEPMSSDDPILGLSSVCILPHIGSATVEARNGM 297

Query: 301 AELVAKNLIAFAKGEIPPNLVNKDV 325
           A L A N+IAF+K E  P   N DV
Sbjct: 298 ARLAAGNIIAFSKNEKMPYCANPDV 322


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: 288
Number of extensions: 10
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: 331
Length of database: 328
Length adjustment: 28
Effective length of query: 303
Effective length of database: 300
Effective search space:    90900
Effective search space used:    90900
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 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