GapMind for Amino acid biosynthesis

 

Alignments for a candidate for aro-dehydratase in Azohydromonas australica DSM 1124

Align arogenate dehydratase (EC 4.2.1.91) (characterized)
to candidate WP_043459340.1 H537_RS0120230 prephenate dehydratase

Query= BRENDA::Q9SGD6
         (413 letters)



>NCBI__GCF_000430725.1:WP_043459340.1
          Length = 368

 Score =  138 bits (348), Expect = 2e-37
 Identities = 108/345 (31%), Positives = 157/345 (45%), Gaps = 45/345 (13%)

Query: 81  IEKSDSNPLV-PQHRHNPLKPLSMTDLSPAPMHGSNL------------------RVAYQ 121
           I+K + +P+  P+     ++ L    ++P P+   NL                  RVA+ 
Sbjct: 43  IKKKEGSPVFRPEREQQVIEGLKA--VNPGPLRNENLAPIWRELMSACRALETPTRVAFL 100

Query: 122 GVPGAYSEAAAGKAY-PNCQAIPCDQFEVAFQAVELWIADRAVLPVENSLGGSIHRNYDL 180
           G  G +SE AA   +  +   +PC   +  F+A     AD  V+PVENS  G++ R+ DL
Sbjct: 101 GPAGTFSEEAALNYFGSSIVRVPCASIDEVFRATSAGSADFGVVPVENSTEGAVARSMDL 160

Query: 181 LLRHRLHIVGEVQLPVHHCLLALPGVRKEF--LTRVISHPQGLAQCEHTLTKLGLNVARE 238
            L   L IVGE  L V H LL L   R++   +  V +HPQ L QC   L++    V R 
Sbjct: 161 FLTTPLSIVGETSLLVRHNLLRL---REDLDGIQAVCAHPQALGQCHEWLSQHLPGVERR 217

Query: 239 AVDDTAGAAEFIASNNLRDTAAIASARAAEIYGLEILEDGIQDDVSNVTRFVMLAREPI- 297
            V   A  A   A +     AA+AS RA   +GL ++  G+QDD  N TRFVM+A     
Sbjct: 218 PVASNAEGARLAAQD--PSLAALASVRAGNEFGLHLVAPGVQDDPRNRTRFVMVADPQCQ 275

Query: 298 -IPRTDRPFKTSIVFAHEKGTSVLFKVLSAFAFRDISLTKIESRPNHNRPIRVVDDANVG 356
            +P       TS+V A       +  +L       +S+T+ ESRP               
Sbjct: 276 SLPAPSGMDCTSLVVAVANRPGAMVDLLVPLKAAGVSMTRFESRP--------------A 321

Query: 357 TAKHFEYMFYVDFEASMAEARAQNALAEVQEFTSFLRVLGSYPMD 401
            +  +EY FYVD +    E     AL  ++   SF ++LG YP+D
Sbjct: 322 RSGQWEYYFYVDLQGHPEEPHVAQALQTLRAHCSFFKLLGGYPLD 366


Lambda     K      H
   0.317    0.131    0.381 

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: 340
Number of extensions: 16
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: 413
Length of database: 368
Length adjustment: 30
Effective length of query: 383
Effective length of database: 338
Effective search space:   129454
Effective search space used:   129454
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 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