GapMind for Amino acid biosynthesis

 

Alignments for a candidate for aro-dehydratase in Allochromatium vinosum DSM 180

Align arogenate dehydratase (EC 4.2.1.91) (characterized)
to candidate WP_012971278.1 ALVIN_RS10390 prephenate dehydratase

Query= BRENDA::Q9SSE7
         (381 letters)



>NCBI__GCF_000025485.1:WP_012971278.1
          Length = 367

 Score =  147 bits (371), Expect = 5e-40
 Identities = 112/337 (33%), Positives = 170/337 (50%), Gaps = 36/337 (10%)

Query: 45  RIVTVLASLRENDANGRDNSVRAMEVKKIFEDSPLLPKPLSSNQLTESVSNGSRVRVAYQ 104
           R V VL  +++ +    D    A   ++I      L +PL++               A+ 
Sbjct: 59  REVAVLRRIKDANPGPLDGEEVARLFREIMSACLALERPLNA---------------AFL 103

Query: 105 GVRGAYSESAAEKAYPNC---EAVPCEEFDTAFEAVERWLVDRAVLPIENSLGGSIHRNY 161
           G  G ++++AA K + +    +A+P    D  F  VE    D  V+P+ENS  G +    
Sbjct: 104 GPEGTFTQAAAIKHFGHSVVTQAMPT--IDEIFREVESGACDFGVVPVENSTEGVVSHTL 161

Query: 162 DLLLRHNLHIVGEVKLAVRHCLLANHGVNIEDLRRVLSHPQALAQCENTLTKLGLVREA- 220
           DL +   L I GEV L V   LL     ++  +RRV SH Q+LAQC   L +   + E  
Sbjct: 162 DLFMNSPLMITGEVSLRVHQHLLTK-AADLASIRRVYSHQQSLAQCREWLDRHLPIAERL 220

Query: 221 -VDDTAGAAKQIAFENLNDAAAVASEKAAKIYGLNIVAKDIQDDCDNVTRFLMLAREPII 279
            V   A AA+ +A +   +AAAVA  +AA+IYGL ++A+ I+D+  N TRFL++ ++   
Sbjct: 221 PVGSNAEAARLVASDP--EAAAVAGLQAAEIYGLRVLAERIEDEPSNTTRFLVIGKQDSP 278

Query: 280 PGTNRLFKTSIVFSLEEGPGVLFKALAVFALRQINLTKIESRPLRKHPLRASGGLKYFDY 339
           P      KTS++ S +   G L   LA  A+  I++T+IESRP R+           +DY
Sbjct: 279 PSGQD--KTSLLLSCKNQSGGLHSLLAPLAVHGISMTRIESRPSRR---------GIWDY 327

Query: 340 LFYVDFEASMADEVAQNALRHLEEFATFLRVLGSYPV 376
           +F+VD      D     AL++LE+ A   +VLGSYPV
Sbjct: 328 VFFVDILGHRQDPKVAYALQNLEQDALLFKVLGSYPV 364


Lambda     K      H
   0.319    0.134    0.384 

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: 271
Number of extensions: 15
Number of successful extensions: 5
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: 381
Length of database: 367
Length adjustment: 30
Effective length of query: 351
Effective length of database: 337
Effective search space:   118287
Effective search space used:   118287
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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