GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Halomonas desiderata SP1

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate WP_086509657.1 BZY95_RS09260 asparaginase

Query= curated2:Q9HJJ5
         (409 letters)



>NCBI__GCF_002151265.1:WP_086509657.1
          Length = 350

 Score =  117 bits (294), Expect = 4e-31
 Identities = 96/333 (28%), Positives = 146/333 (43%), Gaps = 35/333 (10%)

Query: 67  DRKISVLATGGTIASRVDYETGAVSPVSDPELIFGGSDILTRFTVAVKPILNEF------ 120
           DR + VL TGGT+      E   + P  D E     +  L     + +  L EF      
Sbjct: 8   DRPVLVLYTGGTLGMMPSAE--GLVPAGDIETRLRNA--LDGLPPSRQSQLPEFVVHTVA 63

Query: 121 ----SENLKPADWIRIGQAVADESSEADGVVVAHGTDTMAYTSSALAFMFERMRVPVVFV 176
               S    P DW R+   +AD   +  G+VV HGTDT+A+++S+LAF  + +  PVV  
Sbjct: 64  SPIDSSAATPHDWQRLAATIADRIGQHAGIVVLHGTDTLAWSASSLAFQLQGLDRPVVVT 123

Query: 177 GAQRSSDRPSSDSRENMQAAINFAG-TDLGEVGISMHASTSDGHVSLLRSVRSRKMHTSR 235
           GA    +   SD+  N++ A+ FA   +L E+ ++           LLR  RS K H+  
Sbjct: 124 GAMHPLEAEGSDALANIELALRFAARPELQEIAVAFAG-------RLLRGARSSKTHSEN 176

Query: 236 RDAFESIGIPPLAEYDGSVKFLIDYRRVS---------DTVEFRPDLDDRVSMIYFHPGL 286
            DAF S   P L E  G    L   R +          +  ++ P     V  +   PG+
Sbjct: 177 DDAFASPNYPLLGEQVGDDVVLYPARCLETQQRGAPRFELPDYSPLAKGGVVRLALWPGI 236

Query: 287 NAGDLENMIAEKHA----VVILGTGLGHMAKDLIPVVKKYTADGNYAIMASQCIYGSTDL 342
            A  LE  + +       + + G G      ++I V+ K + +G      SQC +G    
Sbjct: 237 QAWQLEAWLGDDRVQGALLEVWGGGNIPPDPEVIGVLAKASGEGKLIAAISQCRWGGIAP 296

Query: 343 NVYSTGRELLAAGVIEAGNMVPEVAYVKAMYLL 375
             Y+ G+ L+ AGV+   +M PE A  K ++LL
Sbjct: 297 GRYAAGQGLIEAGVLSGDDMTPEAAITKLVHLL 329


Lambda     K      H
   0.317    0.135    0.376 

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: 303
Number of extensions: 15
Number of successful extensions: 4
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: 409
Length of database: 350
Length adjustment: 30
Effective length of query: 379
Effective length of database: 320
Effective search space:   121280
Effective search space used:   121280
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 (21.7 bits)
S2: 50 (23.9 bits)

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