GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Bacillus alkalinitrilicus DSM 22532

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_078430189.1 BK574_RS22720 branched-chain-amino-acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_002019605.1:WP_078430189.1
          Length = 301

 Score =  126 bits (317), Expect = 5e-34
 Identities = 100/308 (32%), Positives = 156/308 (50%), Gaps = 44/308 (14%)

Query: 9   YFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAK 68
           Y   +FV   +AK+SV  H   YG   F G+R + D        +F+L  H +RL  SAK
Sbjct: 7   YLNGEFVEKHNAKVSVYDHGFLYGDGVFEGIR-VYDGN------IFQLKEHLERLYNSAK 59

Query: 69  FLHYDI--SAEKIKEVIVDFVKKNQPDKSFYIRPLVYSSGLG----------------IA 110
            +   I  S E++ ++IV+ +K N+   + YIR LV S G+G                IA
Sbjct: 60  SILLTIPHSLEELTQIIVETIKINELQDA-YIR-LVVSRGVGNLGLDPASCPTPNVIVIA 117

Query: 111 PRLHNLEKDFLVYGLEMGDYLAADGVSCRISSWYRQEDRSFPLRGKI-SAAYITSALAKT 169
            +L    K+    GLE             I +   + +R   L  K+ S  Y+ + L K 
Sbjct: 118 EQLSIFPKELYDKGLE-------------IVTVATRRNRPDVLSPKVKSLNYLNNILVKI 164

Query: 170 EAVESGFDEAILMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADL 229
           EA  +G  EA+++N++G V E +  NVF+V+  +I+TP      LEGITR++I+ IA DL
Sbjct: 165 EASLAGVSEALMLNNEGYVAEGSADNVFIVKGNKILTPPGYIGALEGITRNAIIDIAKDL 224

Query: 230 GIPTCQRPIDKSELMIADEVFLSGTAAKITPVKRIENFTLGGDRPITEK---LRSVLTAV 286
           G    + P  + ++ +ADEVFL+GTAA++  V +++   +G  +P  E    L++    V
Sbjct: 225 GYEVKEEPFTRHDVYVADEVFLTGTAAEVIAVVKVDGRVIGDGKPGKETNKLLQAFRQKV 284

Query: 287 TENREPKY 294
            E+ E  Y
Sbjct: 285 VEDGEKVY 292


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: 203
Number of extensions: 11
Number of successful extensions: 2
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: 301
Length adjustment: 27
Effective length of query: 278
Effective length of database: 274
Effective search space:    76172
Effective search space used:    76172
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 Apr 10 2024. The underlying query database was built on Apr 09 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