GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Clostridium tyrobutyricum FAM22553

Align Glyoxylate reductase; EC 1.1.1.26 (uncharacterized)
to candidate WP_017751038.1 PN53_RS06710 D-glycerate dehydrogenase

Query= curated2:B1L765
         (332 letters)



>NCBI__GCF_000816635.1:WP_017751038.1
          Length = 323

 Score =  261 bits (666), Expect = 2e-74
 Identities = 139/319 (43%), Positives = 207/319 (64%), Gaps = 3/319 (0%)

Query: 2   KPRVFVTREIPERGLSKIEEHFELDLWKDEAPPSKKVIIERVKDCDALVSLLTDPIDAEV 61
           KP+VF+ + IPE   + +E++ E   W      S++ + + +KD +  +    + ID E+
Sbjct: 3   KPKVFIGKSIPEEVKNYLEQYCECKYWNSNNAISRQQLFKELKDVEGFLES-GEEIDDEL 61

Query: 62  FEAAPKLRIVAQYAVGYDNIDVKEATKRGIYVTNTPGVLTETTADFAFALLMAAARRVVE 121
              AP L+IV+  +VGY+N  ++    +G+  TNTP VL +T AD  F+L+++ ARR+ E
Sbjct: 62  LLHAPNLKIVSNSSVGYNNFHLQSMKSKGVIGTNTPFVLDDTVADLVFSLVISTARRIPE 121

Query: 122 ADRYVREGKWKVAWHPMMMLGYDVYGRTLGIVGMGRIGAAVARRAK-GFGMRILYYDSIR 180
            D YV+ GKWK + +  +  G DV+  TLGI+GMGRIG  VA+RA+ GF M +LY++  R
Sbjct: 122 MDSYVKHGKWKSSDNENLY-GVDVHHATLGIIGMGRIGQKVAKRARLGFSMDVLYHNRSR 180

Query: 181 REDFEKELGVEYVPLEKLLEESDFVSLHVPLTEETYHMIGEEQLRRMKRTAILVNTSRGK 240
           + D E +LGV+YV L+ LL +SD++ L +PLT+ET H+I  ++   MK TAI +N SRGK
Sbjct: 181 KFDTESKLGVKYVSLDTLLIQSDYIVLMIPLTQETMHLIDYKEFDLMKDTAIFINASRGK 240

Query: 241 VVDQKALYKALKEGWIAGAGLDVFEQEPIPPDDPLLKLENVVLAPHAASASHETRSRMAE 300
            V++KAL  AL+   I GAGLDV+ QEP+  ++PLLK+ NVV  PH  SA+ +TR  M  
Sbjct: 241 TVNEKALIDALENKKILGAGLDVYAQEPVNKNNPLLKMSNVVTLPHIGSATEKTRFSMDM 300

Query: 301 MVAENLIAFKRGEIPPNLV 319
             AENL++   G+IP  +V
Sbjct: 301 TAAENLVSGLIGKIPKYIV 319


Lambda     K      H
   0.319    0.137    0.398 

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: 264
Number of extensions: 12
Number of successful extensions: 4
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: 332
Length of database: 323
Length adjustment: 28
Effective length of query: 304
Effective length of database: 295
Effective search space:    89680
Effective search space used:    89680
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 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