GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gyaR in Pseudomonas simiae WCS417

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate GFF5281 PS417_27040 3-phosphoglycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>lcl|FitnessBrowser__WCS417:GFF5281 PS417_27040 3-phosphoglycerate
           dehydrogenase
          Length = 409

 Score =  171 bits (433), Expect = 3e-47
 Identities = 101/293 (34%), Positives = 158/293 (53%), Gaps = 14/293 (4%)

Query: 35  PRGVLLEKVREVDALVTLVTDKVDKELLENAPKLKIIAQYAVGYDNIDIEEATKRGIYVT 94
           P   L EK+ +   +      ++ +E+ ++A KL  +  + +G + +D+  A +RGI V 
Sbjct: 43  PEAQLKEKIADAHFIGIRSRTQLTEEIFDHAKKLVAVGCFCIGTNQVDLNAARERGIAVF 102

Query: 95  NTPGVLTDATADLAFALLLAVARRIVEADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLG 154
           N P   T + A+L  A  + + R I E +A    G W KS           + ++GK LG
Sbjct: 103 NAPYSNTRSVAELVLAEAILLLRGIPEKNASCHRGGWIKSAAN-------SFEIRGKKLG 155

Query: 155 IVGFGRIGQALAKRAKGFGMKIIYYSRTRKPEAEEEIGAEYVDFETLLKESDFISLHVPL 214
           IVG+G IG  L+  A+G GM++ +Y    K         +      LL  SD ++LHVP 
Sbjct: 156 IVGYGSIGTQLSVLAEGLGMQVFFYDTLTKLPLGN--ATQVASLTELLGMSDIVTLHVPE 213

Query: 215 TKETYHMIGEKELKLMKPNAILINTSRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYN 274
           T ET  MIGEKE++ +K   ILIN +RG VV+ +AL  A+K+  + GA +DVF EEP  N
Sbjct: 214 TAETQWMIGEKEIRAIKKGGILINAARGTVVELDALADAIKDKHLIGAAIDVFPEEPRSN 273

Query: 275 EELFK-----LKNVVLAPHIGSATHEAREGMAELVAKNLIAFAKGEIPPNLVN 322
           +++F+     L NV+L PHIG +T EA+  +   V++ L+ ++      + VN
Sbjct: 274 DDIFESPLRGLDNVILTPHIGGSTAEAQANIGLEVSEKLVKYSDNGTSVSSVN 326


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: 309
Number of extensions: 18
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: 409
Length adjustment: 30
Effective length of query: 301
Effective length of database: 379
Effective search space:   114079
Effective search space used:   114079
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.

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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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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