GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Burkholderia phytofirmans PsJN

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate BPHYT_RS14520 BPHYT_RS14520 2-hydroxyacid dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>FitnessBrowser__BFirm:BPHYT_RS14520
          Length = 329

 Score =  260 bits (664), Expect = 4e-74
 Identities = 143/328 (43%), Positives = 204/328 (62%), Gaps = 11/328 (3%)

Query: 4   KVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKELLE 63
           K+ + R I  + I+ ++++++++ W          L  ++ + D  +T   D V    L 
Sbjct: 3   KILVARPIFPDVIERLKQYFDVD-WNQGDVLAADELKRRLADKDGALT-AGDPVGAAELA 60

Query: 64  NAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEAD 123
            AP+L++++  AVGY+N D+       +  TNTP VL ++TAD  +AL++A ARRI E++
Sbjct: 61  AAPRLRVVSNMAVGYNNFDVAAFNAANVLGTNTPDVLNESTADFGWALMMAAARRITESE 120

Query: 124 AFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYSRTR 183
            ++R G+W+K    W    FLG  L G TLG++G GRIGQALA+RAKGF M++IY++R+R
Sbjct: 121 HWLRGGQWQK----WAYDAFLGSDLHGSTLGVIGMGRIGQALARRAKGFDMQVIYHNRSR 176

Query: 184 -KPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTSRG 242
             PE E E+ AEYV  + LL+ +D + L +P TKE +H IG  EL LMKP A L N +RG
Sbjct: 177 VAPEIEAELNAEYVSKQDLLRRADHVVLVLPYTKENHHTIGAAELALMKPTATLTNIARG 236

Query: 243 AVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREGMAE 302
            +VD  AL++AL+   IA AGLDVFE EP  N++L  + NVVL PHI SAT   R  MA 
Sbjct: 237 GIVDDAALVEALRSKQIAAAGLDVFEGEPNLNQDLLSVPNVVLTPHIASATEATRRAMAN 296

Query: 303 LVAKNLIA----FAKGEIPPNLVNKDVL 326
           L A NLIA      +   PPN VN +V+
Sbjct: 297 LAADNLIAGLGEGPRAGRPPNPVNPEVI 324


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: 278
Number of extensions: 9
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: 329
Length adjustment: 28
Effective length of query: 303
Effective length of database: 301
Effective search space:    91203
Effective search space used:    91203
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