GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Pseudomonas fluorescens FW300-N2C3

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate AO356_16925 AO356_16925 bifunctional glyoxylate/hydroxypyruvate reductase B

Query= SwissProt::Q9C4M5
         (331 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_16925
          Length = 323

 Score =  270 bits (691), Expect = 3e-77
 Identities = 153/326 (46%), Positives = 213/326 (65%), Gaps = 6/326 (1%)

Query: 1   MKPKVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKE 60
           MK  V    +I    I+ + + +E+ +             E +  V  L+  V  K+ +E
Sbjct: 1   MKKTVLAFSRITPPMIERLRQDFEVIVPNPSHGDINAQFNEALPHVHGLIG-VGRKLGRE 59

Query: 61  LLENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIV 120
            L++A  L++++  +VGYDN D+    +RGI +TNTP VLT++TADLAFALL++ ARR+ 
Sbjct: 60  QLQSATNLQVVSSVSVGYDNYDLAYFNERGIMLTNTPDVLTESTADLAFALLMSSARRVA 119

Query: 121 EADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAK-GFGMKIIYY 179
           E DA+ ++G+W+ + VG  P +F G  + GKTLGIVG G IG A+A+R + GF M IIY 
Sbjct: 120 ELDAWTKAGQWQAT-VG--PQLF-GSDVHGKTLGIVGMGNIGAAIARRGRLGFNMPIIYS 175

Query: 180 SRTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINT 239
             +RK E E ++GA++ + + LL E+DF+ L VPL+++T H+IG++EL LMKP+AIL+N 
Sbjct: 176 GNSRKTELENQLGAQFRELDQLLAEADFVCLVVPLSEKTRHLIGQRELGLMKPSAILVNI 235

Query: 240 SRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREG 299
           SRG VVD  ALI+AL+   I GAGLDV+E+EP     LF+LKN V  PHIGSATHE RE 
Sbjct: 236 SRGPVVDEPALIEALQNNRIRGAGLDVYEKEPLAESPLFQLKNAVTLPHIGSATHETREA 295

Query: 300 MAELVAKNLIAFAKGEIPPNLVNKDV 325
           MA L   NL +   GE P NLVN  V
Sbjct: 296 MANLAVDNLRSALLGERPQNLVNPQV 321


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: 260
Number of extensions: 14
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: 323
Length adjustment: 28
Effective length of query: 303
Effective length of database: 295
Effective search space:    89385
Effective search space used:    89385
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:

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