GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Sulfurivirga caldicuralii DSM 17737

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_074200794.1 BUQ81_RS02440 branched-chain amino acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_900141795.1:WP_074200794.1
          Length = 310

 Score =  176 bits (447), Expect = 5e-49
 Identities = 107/300 (35%), Positives = 169/300 (56%), Gaps = 13/300 (4%)

Query: 7   IAYFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKS 66
           + +F+ + VP+ +AK+ V TH LHYG   F G+R      + GT + FRL+ H  RL  S
Sbjct: 11  LIWFDGEMVPWREAKVHVLTHTLHYGMGVFEGVRAYES--ELGTAI-FRLEEHTQRLINS 67

Query: 67  AKFLHYDIS--AEKIKEVIVDFVKKNQPDKSFYIRPLVYSSGLGIAPRLHNLEKDFLVYG 124
           AK +   ++  AE++ E     V++N   +S YIRP+V+    G+  R  NL+   +V  
Sbjct: 68  AKIMQMPLNYTAEELNEAQRAAVRENGL-RSAYIRPMVFYGSEGMGLRADNLKAHVIVAA 126

Query: 125 LEMGDYLAAD----GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAI 180
            E G Y+  +    G+    SS+ R        R K +  YI S LA  EA+  G DEA+
Sbjct: 127 WEWGAYMGEENLKRGIKVATSSFTRHHVNITMTRAKANGNYINSMLALQEAISHGADEAL 186

Query: 181 LMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDK 240
           L++ +G V E +G N FM+++G I TP      L+GITR +++ +A ++G    ++ I +
Sbjct: 187 LLDPEGYVAEGSGENFFMIKDGVIYTP-ELTSCLDGITRKTVMQLAREMGYEIVEKRITR 245

Query: 241 SELMIADEVFLSGTAAKITPVKRIENFTLG-GDR-PITEKLRSVLTAVTENREPKYQDWV 298
            E+ IADE F +GTAA++TP++ ++   +G G R PITEKL+     V   R P+++ W+
Sbjct: 246 DEVYIADEAFFTGTAAEVTPIRELDGRVIGAGSRGPITEKLQQRYFDVVHGRAPEHRRWL 305


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: 230
Number of extensions: 10
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: 305
Length of database: 310
Length adjustment: 27
Effective length of query: 278
Effective length of database: 283
Effective search space:    78674
Effective search space used:    78674
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: 48 (23.1 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