GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Persephonella marina EX-H1

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_015898939.1 PERMA_RS06100 branched-chain amino acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000021565.1:WP_015898939.1
          Length = 302

 Score =  221 bits (563), Expect = 2e-62
 Identities = 118/298 (39%), Positives = 182/298 (61%), Gaps = 6/298 (2%)

Query: 9   YFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAK 68
           YFE K VP + AKIS+ T++ HYGTA F G+R   D +      LF    H +RL ++ K
Sbjct: 5   YFEGKIVPEDQAKISIKTNSFHYGTAIFEGIRAYYDKDTDRMWGLF-FKEHYERLFQNMK 63

Query: 69  FLHYDI--SAEKIKEVIVDFVKKNQPDKSFYIRPLVYSSGLGIAPRLHNLEKDFLVYGLE 126
            L+ +I  S +++ E+  + ++KN      YIRP+VY S L I+P+L   +    +Y   
Sbjct: 64  VLNMEIEESIDQLVEITKELIRKNNIKDDIYIRPIVYFSDLKISPKLVGYKSRIAIYTYP 123

Query: 127 MGDYLAAD-GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAILMNSQ 185
           +GDY+  + G+   +SSW R  D   P R K++ +Y+ SA +KTEA+ +G DEAI++N  
Sbjct: 124 LGDYIDINKGIKAIVSSWTRINDNMIPPRLKVAGSYVNSAFSKTEAILAGADEAIVLNKN 183

Query: 186 GKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDKSELMI 245
           G V E +  N+F+VR+G+++TP    DILEGITR++I+TIA DLG    +R I ++EL I
Sbjct: 184 GYVSEGSAENIFIVRDGKLITPPVSDDILEGITRNAIITIAKDLGYQVIERHISRTELYI 243

Query: 246 ADEVFLSGTAAKITPVKRIENFTLGGDRP--ITEKLRSVLTAVTENREPKYQDWVFKI 301
           ADE+F  GT A+++PV  +++  +G   P  IT++++ V       +  KY+ WV  I
Sbjct: 244 ADEIFFCGTGAQVSPVVEVDHRKIGDGSPGKITKEIQEVYFNAVRGKIEKYRHWVIPI 301


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: 233
Number of extensions: 12
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: 302
Length adjustment: 27
Effective length of query: 278
Effective length of database: 275
Effective search space:    76450
Effective search space used:    76450
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