GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Hydrogenovibrio marinus DSM 11271

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95; 2-oxoglutarate reductase; EC 1.1.1.399 (uncharacterized)
to candidate WP_029912676.1 P166_RS0111135 4-phosphoerythronate dehydrogenase

Query= curated2:P35136
         (525 letters)



>NCBI__GCF_000711315.1:WP_029912676.1
          Length = 374

 Score =  112 bits (280), Expect = 2e-29
 Identities = 106/332 (31%), Positives = 159/332 (47%), Gaps = 44/332 (13%)

Query: 25  EIVQKNVADAEDELHTFDALLVRSATKVTEDLFNKMTSLKIVGRAGVGVDNIDIDEATKH 84
           EI  + V DA       DAL+VRS T+V + L  K +S++ VG   VG+D+ID D     
Sbjct: 30  EITSETVKDA-------DALIVRSRTQVNQSLL-KNSSVEFVGSTVVGLDHIDQDYLASK 81

Query: 85  GVIVINAPNGNTISTAEHTFAMISSLMRHIPQANISVKSREWNRTAYVGSELYGKTLGIV 144
            +   +A   N  S +E+   +IS+L+ H  + +              G EL  K+LGI+
Sbjct: 82  NIHFYSAQGCNANSVSEY---VISALL-HFAEEH--------------GFELSEKSLGII 123

Query: 145 GLGRIGSEIAQRARAFGMTVHVFDPFLTEERAKKIGVNSRTFEEVLESADIITVHTPLTK 204
           G+G +G  + Q+A A GMTV + DP     R +K  +      +   SADII+ HTPLTK
Sbjct: 124 GVGNVGKLLEQKAIALGMTVFLNDP----PRQEKEDLPHFVDLDKALSADIISFHTPLTK 179

Query: 205 ETK----GLLNKETIAKTKKGVRLINCARGGIIDEAALLEALENGHVAGAALDVFEVEPP 260
           + K     LLN+           +IN ARGGIIDE+   +   + ++    +D +E EP 
Sbjct: 180 DGKYPSHHLLNQNNFHLIHPSTVVINAARGGIIDESVWSKTETDINI----IDCWENEPN 235

Query: 261 VDNKLVDHPLVIATPHLGASTKEAQLNVAAQVSEEVLQFAKGLPVMS--AINLPAMTKDE 318
           +D  L      IATPH+     EA++  ++ V E + Q     P+ S     +P  T+  
Sbjct: 236 IDANLY-QKADIATPHIAGHALEAKIKGSSMVYEVLCQH-WNQPIQSHWKAQVPHPTEPL 293

Query: 319 FAKIKPYHQIAGKIGSLVSQCMKEPVQDVAIQ 350
            A      Q    +  LV  C    + D+AI+
Sbjct: 294 TASYGDSFQ--SMLFKLVHHCYDPVIDDLAIR 323


Lambda     K      H
   0.317    0.134    0.373 

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: 416
Number of extensions: 26
Number of successful extensions: 6
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: 525
Length of database: 374
Length adjustment: 32
Effective length of query: 493
Effective length of database: 342
Effective search space:   168606
Effective search space used:   168606
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: 51 (24.3 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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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