GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Paraburkholderia bryophila 376MFSha3.1

Align D-3-phosphoglycerate dehydrogenase (characterized, see rationale)
to candidate H281DRAFT_06499 H281DRAFT_06499 D-3-phosphoglycerate dehydrogenase

Query= uniprot:Q5JGC4
         (304 letters)



>FitnessBrowser__Burk376:H281DRAFT_06499
          Length = 306

 Score =  190 bits (482), Expect = 4e-53
 Identities = 117/305 (38%), Positives = 178/305 (58%), Gaps = 13/305 (4%)

Query: 3   VLVAAPLHEKAIEVLKNAGFEVVYE-EYPDEDRLVELVKDVD--AIIVRSKPKVTRKVIE 59
           ++  A L  +A+ +L  A +E+VY    P  D L+ L +  +  AIIVR    VT  +++
Sbjct: 8   LVTGADLAPQAVALL--ADYEIVYAGATPGPDELLRLARQHNPTAIIVRFGG-VTPVIMD 64

Query: 60  AAPKLKVIGRAGVGLDNIDLKAAEERGIKVVNSPGASSRSVAELAIGLIFAVARKIAFAD 119
           AAP LKVI + G G D ID +AA ER IKVV + G+++ +VAE A+ L  A A+ +    
Sbjct: 65  AAPALKVISKHGSGTDTIDKQAAAERNIKVVAAVGSNAAAVAEQALALTLACAKSVVKLH 124

Query: 120 RKMREGVWAKKQCMGIELEGKTIGVVGFGRIGYQVAKIANALGMKVLFYDPYPNEERAKE 179
            +M+ G W K     +EL GKTIG++G G IG + A++  AL M+VL +DPY     AK+
Sbjct: 125 ERMQAGHWDKATHKNVELNGKTIGLIGLGAIGRKFARMVEALDMRVLGFDPY-----AKD 179

Query: 180 VGGKF--ADLETLLKESDVVTLHVPLVDATYHLINEERLKLMKPTAILINAARGAVVDTD 237
           +       DL T+ +ES+V++ H PL     +++N + L   K   I++N ARG +++  
Sbjct: 180 LPHYIQPVDLGTIWRESNVLSFHCPLTADNRNMLNAQTLAQCKKGVIVVNTARGGLIEEP 239

Query: 238 ALVKALQEGWIAGAGLDVFEEEPLPADHPLTKLDNVVLTPHIGASTVEAQMRAGVEVAEK 297
           AL+ A+Q G +A AGLD F  EPL   H     + ++L+PHIG +T +A +  GV  A  
Sbjct: 240 ALLAAVQSGQVAMAGLDSFAIEPLAVPHMFRNQERIILSPHIGGTTSDAVVSMGVAAARN 299

Query: 298 IVEAL 302
           I+ A+
Sbjct: 300 ILAAM 304


Lambda     K      H
   0.317    0.136    0.378 

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: 226
Number of extensions: 9
Number of successful extensions: 2
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: 304
Length of database: 306
Length adjustment: 27
Effective length of query: 277
Effective length of database: 279
Effective search space:    77283
Effective search space used:    77283
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 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