GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Phaeobacter inhibens BS107

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate GFF2783 PGA1_c28260 glyoxylate reductase GyaR

Query= SwissProt::Q9C4M5
         (331 letters)



>FitnessBrowser__Phaeo:GFF2783
          Length = 328

 Score =  263 bits (671), Expect = 6e-75
 Identities = 144/325 (44%), Positives = 206/325 (63%), Gaps = 7/325 (2%)

Query: 5   VFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKELLEN 64
           V +TR++PE     + + +++ L +D     R  L   +++ D LV  VTD++D  LL  
Sbjct: 8   VVVTRRLPEPVETRLSELFDVRLREDDTPMSRAELATALKDADVLVPTVTDEIDAGLLGQ 67

Query: 65  A-PKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEAD 123
           A  +LK+IA Y  G D+ID+  A +RGI V+NTPGVLTD TAD+A AL++AV RRI E  
Sbjct: 68  AGDRLKLIANYGAGVDHIDVATARQRGILVSNTPGVLTDDTADMAMALIMAVVRRIPEGL 127

Query: 124 AFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYSRTR 183
           A ++ G+W+    GW P   LG  L G+ LGI+G G IGQA+AKRA  FGM++ Y++R R
Sbjct: 128 AVMQKGDWQ----GWSPTALLGGRLAGRRLGILGMGSIGQAVAKRAAAFGMQVHYHNRRR 183

Query: 184 -KPEAEEEIGAEYVD-FETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTSR 241
            +PE E+   A Y +  + ++   D +S++ P T  T+H++  + LKLMKP+A+++NTSR
Sbjct: 184 LRPEIEQRFEATYWESLDQMVARMDVLSINCPSTPSTFHLMNARRLKLMKPDAVIVNTSR 243

Query: 242 GAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREGMA 301
           G V+D +AL + L+   IAGAGLDV+E     N  L +L+NVVL PH+GSAT E R  M 
Sbjct: 244 GEVIDEHALTRMLRASEIAGAGLDVYEHGTDINPRLRELENVVLLPHMGSATLEGRLEMG 303

Query: 302 ELVAKNLIAFAKGEIPPNLVNKDVL 326
           E V  N+  F  G  PP+ V   +L
Sbjct: 304 EKVLLNIKTFEDGHRPPDQVVPSML 328


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: 256
Number of extensions: 8
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: 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 17 2021. 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