GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Trichlorobacter lovleyi SZ

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_012470683.1 GLOV_RS13060 branched-chain amino acid aminotransferase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000020385.1:WP_012470683.1
          Length = 359

 Score = 96.3 bits (238), Expect = 9e-25
 Identities = 93/311 (29%), Positives = 137/311 (44%), Gaps = 36/311 (11%)

Query: 16  PFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAKFLHYDIS 75
           P+E   +  AT  LHY    F GL+      D G I LFR + +  R ++SA  +     
Sbjct: 51  PYEPFMLDPATTVLHYAQEIFEGLKAYK--WDDGRIALFRPEMNARRFNQSASRM---CM 105

Query: 76  AEKIKEVIVDFVKK----------NQPDKSFYIRPLVYSSG--LGIAPRLHNLEKDFLVY 123
            E  +E+ +D + K          + P  + YIRP + +    LG+ P  H     F V 
Sbjct: 106 PEVPEELFLDGIDKLVELEKDWIPSAPGTAMYIRPAMIAVDPYLGVKPGDHYY---FFVI 162

Query: 124 GLEMGDYLAA--DGVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAIL 181
              +G Y AA  + VS  +   Y +         K    Y +S  A  EA + GFD+ + 
Sbjct: 163 LSPVGAYYAAGFNPVSILVEDKYVRSVAGGTGDAKTGGNYASSLKAGLEAKKKGFDQVLW 222

Query: 182 MNSQGK--VCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPID 239
           ++ + +  + E   MN+F      IVT      IL GITR+S+L +A +LG    +R ID
Sbjct: 223 LDGKERRYIEEVGAMNMFFAYGNHIVTAPLTGSILSGITRESVLRLAIELGCTVEERLID 282

Query: 240 KSELMI------ADEVFLSGTAAKITPVKRI--ENFTL----GGDRPITEKLRSVLTAVT 287
             EL          E F SGTAA +TPV  +  ++  L    GG   IT+KL   LT + 
Sbjct: 283 VDELFADLRNGKVTEAFGSGTAAVVTPVGTLGYKDEALQVGDGGVGAITQKLYDALTGIQ 342

Query: 288 ENREPKYQDWV 298
             +      W+
Sbjct: 343 TGKLDDRYGWI 353


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: 278
Number of extensions: 18
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: 305
Length of database: 359
Length adjustment: 28
Effective length of query: 277
Effective length of database: 331
Effective search space:    91687
Effective search space used:    91687
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