GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gyaR in Phaeobacter inhibens BS107

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate GFF2436 PGA1_c24680 glyoxylate reductase GyaR

Query= SwissProt::Q9C4M5
         (331 letters)



>FitnessBrowser__Phaeo:GFF2436
          Length = 318

 Score =  220 bits (561), Expect = 3e-62
 Identities = 129/318 (40%), Positives = 181/318 (56%), Gaps = 9/318 (2%)

Query: 1   MKPKVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKE 60
           M  K++ITR +           +  E+ ++      G     +RE D ++  + D+ D  
Sbjct: 1   MSGKLWITRPMTAAVEARARSEFGAEIRQETTPLTAGERQRALREFDVVMPTLGDQFDAA 60

Query: 61  LLE--NAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARR 118
                +AP+ +++A + VGY++ID++ A   GI V+NTPG +TDATAD A  L+L  ARR
Sbjct: 61  SFAGVSAPRCRLLANFGVGYNHIDVDAAKTAGIAVSNTPGAVTDATADTALTLMLMTARR 120

Query: 119 IVEADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAK-GFGMKII 177
             E +  VRSG+W+    GWHP   LG  L GK +GIVGFGRIG+A+A+R   GFGM + 
Sbjct: 121 AGEGERLVRSGQWQ----GWHPTQMLGLHLTGKHVGIVGFGRIGEAIARRCHFGFGMSVS 176

Query: 178 YYSRTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILI 237
           Y +R+ K      + A+      L    D + L VP   ET H+I  + L  M+P A+LI
Sbjct: 177 YLARSEKSPGFPAVRAD--SLTALAASVDVLVLAVPGGAETRHLINAEVLAAMRPEALLI 234

Query: 238 NTSRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAR 297
           N +RG VVD  ALI AL+ G IAGAGLDV+E EP     L +++ V L PH+G+AT E R
Sbjct: 235 NIARGEVVDEAALISALQTGQIAGAGLDVYEFEPEVPLALQQMEQVTLLPHLGTATEEVR 294

Query: 298 EGMAELVAKNLIAFAKGE 315
             M  L   N+ AF  G+
Sbjct: 295 SDMGHLALDNVAAFLAGK 312


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: 213
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: 318
Length adjustment: 28
Effective length of query: 303
Effective length of database: 290
Effective search space:    87870
Effective search space used:    87870
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: 48 (23.1 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