GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Paucidesulfovibrio gracilis DSM 16080

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_078718087.1 B5D49_RS12715 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_900167125.1:WP_078718087.1
          Length = 327

 Score =  305 bits (780), Expect = 1e-87
 Identities = 160/327 (48%), Positives = 217/327 (66%), Gaps = 7/327 (2%)

Query: 3   PKVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKELL 62
           PKV ITR +PE G+  + +  ++   K  +   R  LLE V++   ++ L+TD++D E  
Sbjct: 4   PKVVITRPLPEAGLSQLREQVQLVENKKDRPMQRTELLEAVQDAHGVIGLLTDRIDAEFF 63

Query: 63  ENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEA 122
           + APKL   A YAVGYDNID+ EAT+RGI V+NTP VLT ATA+LA+ LL AVARRIVE 
Sbjct: 64  DAAPKLVGYANYAVGYDNIDVTEATRRGIPVSNTPDVLTRATAELAWGLLFAVARRIVET 123

Query: 123 DAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYY--- 179
           D  +RSG W     GW P+ ++G  + G+TLGIVG GRIG A+A  ++GF M ++Y    
Sbjct: 124 DGVMRSGHWP----GWGPMQYMGMDVSGRTLGIVGAGRIGTAMALMSRGFDMPVLYLESP 179

Query: 180 SRTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINT 239
           S  R    E ++ A+ V +E LL+ SDF+S+H PLT  T H+   +  + MK +AILINT
Sbjct: 180 SGRRNQILESKVNAQCVSWEELLQRSDFVSVHCPLTPATRHLFDRRAFRKMKNSAILINT 239

Query: 240 SRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREG 299
           +RG V+  + L+ AL+EG IAGAGLDV+E+EP   + L  L+  VL PH+GSATH  RE 
Sbjct: 240 ARGPVIKEDDLVAALREGDIAGAGLDVYEKEPVMADGLAALQQAVLLPHVGSATHTTREA 299

Query: 300 MAELVAKNLIAFAKGEIPPNLVNKDVL 326
           MAEL A+NL+A   G +PP  +N +VL
Sbjct: 300 MAELAARNLLAMLHGTVPPTCLNPEVL 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: 254
Number of extensions: 5
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: 327
Length adjustment: 28
Effective length of query: 303
Effective length of database: 299
Effective search space:    90597
Effective search space used:    90597
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 Apr 09 2024. 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