GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Desulfacinum infernum DSM 9756

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95 (uncharacterized)
to candidate WP_073039882.1 BUB04_RS12175 D-glycerate dehydrogenase

Query= curated2:O27051
         (525 letters)



>NCBI__GCF_900129305.1:WP_073039882.1
          Length = 332

 Score =  216 bits (551), Expect = 8e-61
 Identities = 122/318 (38%), Positives = 183/318 (57%), Gaps = 8/318 (2%)

Query: 4   MKVLIADSINEKGISELEEVA-EVVVNTTITP---EELLDAIKDFDAIVVRSRTKVTREV 59
           MKVL+   + ++ + +L     +V  +  + P   EELL  ++  + ++     ++ REV
Sbjct: 7   MKVLVTAKLPDEAVRKLILAGCDVDGHGEVRPMNREELLARVEGAEGLLCTITDRIDREV 66

Query: 60  IEAAPRLKIIARAGVGVDNVDVKAATDRGIMVINAPESTSITVAEHSIGLMLALARKIAI 119
            + AP L++ A  GVG D++DV  A  RGI+V N P+  +   A+ +  L+LA+AR++  
Sbjct: 67  FDKAPGLRVAANYGVGFDHIDVAEAGRRGILVTNTPDVLTDATADLAFALILAVARRVVE 126

Query: 120 ADRSVKEGK---WEKNRFMGIELNGKTLGIIGMGRIGSQVVVRTKAFGMDIM-VYDPYIS 175
            DR  + G+   W    F+G E++GKTLGI+G GRIG  V  R + F M ++      + 
Sbjct: 127 GDRRTRSGQFRFWAPLHFLGTEVSGKTLGIVGFGRIGKAVARRARGFDMQVLYTARKPLE 186

Query: 176 KEAAEEMGVTVTDLETLLRESDIVTIHVPLTPETRHLISEDEFKLMKDTAFIVNCARGGI 235
           K   E +GV    LE LL +SD V++HVPLTP+TRHLI   E  LMK +AF++N ARG +
Sbjct: 187 KREEERLGVRFAPLEELLAQSDFVSLHVPLTPQTRHLIGARELSLMKPSAFLINTARGPV 246

Query: 236 IDEDALYRALKDGEIAGAALDVFEEEPPEGSPLLELENVVLTPHIGASTSEAQRDAAIIV 295
           +DE AL   L+ G I GA LDV+E EP     L +L+NVVL PH+G++T E +   A + 
Sbjct: 247 VDEKALVETLRGGGIRGAGLDVYENEPELTPGLADLQNVVLLPHVGSATVETRTRMAEMA 306

Query: 296 ANEIKTVFQGGAPRNVLN 313
              +     G  P + LN
Sbjct: 307 VENLLEGLAGRRPPHCLN 324


Lambda     K      H
   0.316    0.135    0.366 

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: 365
Number of extensions: 17
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: 525
Length of database: 332
Length adjustment: 31
Effective length of query: 494
Effective length of database: 301
Effective search space:   148694
Effective search space used:   148694
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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