GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Haloechinothrix alba DSM 45207

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_089300747.1 CHB84_RS07365 branched-chain amino acid aminotransferase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_900188115.1:WP_089300747.1
          Length = 367

 Score =  107 bits (266), Expect = 6e-28
 Identities = 92/310 (29%), Positives = 138/310 (44%), Gaps = 29/310 (9%)

Query: 16  PFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAKFLHY--- 72
           P+    +  AT  LHYG A F GL+    P+  G++  FR  ++  R  +SA+ L     
Sbjct: 56  PYGPVTLEPATSVLHYGQAIFEGLKAYRQPD--GSVASFRPQQNAARFRRSARRLAIPEL 113

Query: 73  --DISAEKIKEVIVDFVK--KNQPDKSFYIRPLVYSSGLGIAPRLHNLEKDFLVYGLEMG 128
             ++    I+E+I    +    Q  +S Y+RP   ++   +          + +     G
Sbjct: 114 DEEVFLRSIEELIAVDGRWVPAQEGESLYLRPFTIATEASLGVNRPANRYLYSLIASPAG 173

Query: 129 DYLAAD--GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAILM--NS 184
            Y A     VS  +S+ Y +         K +  Y  S +A+ +AVE G D+ + +  N 
Sbjct: 174 SYFAGGVKPVSVWLSTDYTRAAPGGTGFVKCAGNYAASFVAQAQAVEQGCDQVVWLDANE 233

Query: 185 QGKVCEATGMNVFMV----RNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDK 240
              V E  GMN+F V     N  IVTP     +L G+TRDS++T+  D G P  +R I  
Sbjct: 234 HRWVEEMGGMNLFFVFGSGENAHIVTPELTGTLLPGVTRDSLITLCRDFGYPVTERKIST 293

Query: 241 SELMIA------DEVFLSGTAAKITPVKRIEN----FTLGGDRP--ITEKLRSVLTAVTE 288
            E   A       EVF  GTAA ITPV R+ +    F +GG  P  +T +LR  L  +  
Sbjct: 294 EEWEKAATSGELTEVFACGTAAVITPVGRVRHAGGEFDVGGGDPGEVTMRLRGELIGIQT 353

Query: 289 NREPKYQDWV 298
              P    W+
Sbjct: 354 GTHPDPHGWM 363


Lambda     K      H
   0.320    0.138    0.406 

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: 274
Number of extensions: 23
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: 305
Length of database: 367
Length adjustment: 28
Effective length of query: 277
Effective length of database: 339
Effective search space:    93903
Effective search space used:    93903
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: 49 (23.5 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