GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Hydrogenovibrio kuenenii DSM 12350

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_024850657.1 N745_RS0102995 branched-chain amino acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000526715.1:WP_024850657.1
          Length = 308

 Score =  169 bits (427), Expect = 1e-46
 Identities = 111/300 (37%), Positives = 162/300 (54%), Gaps = 13/300 (4%)

Query: 7   IAYFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKS 66
           + + + + V + +AK  V TH LHYG   F G+R   D E   +I  FRL+ H DRL  S
Sbjct: 10  LIWLDGEMVDWREAKTHVLTHTLHYGMGVFEGVRAY-DAEQGTSI--FRLEAHTDRLFNS 66

Query: 67  AKFLHYDI--SAEKIKEVIVDFVKKNQPDKSFYIRPLVYSSGLGIAPRLHNLEKDFLVYG 124
           AK ++  +  S E+I E     V++N   KS YIRP+V+    G+  R  NL+   +V  
Sbjct: 67  AKIMNMAMPFSKEEINEAQRAAVRENNL-KSAYIRPMVFYGSEGMGLRADNLKTHIVVAA 125

Query: 125 LEMGDYLAAD----GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAI 180
            E G Y+  +    G+    SS+ R        + K +  Y+ S LA  EA   G DEA+
Sbjct: 126 WEWGAYMGEENLQRGIKIATSSFTRHHPNITMTKAKSNGQYMNSMLALQEATSHGCDEAL 185

Query: 181 LMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDK 240
           L++  G V E +G N FMV+ G I TP      L+GITR +I+  A + G    +R I +
Sbjct: 186 LLDKDGFVSEGSGENFFMVKEGVIYTP-FLTSALDGITRKTIIQFAKEEGFEVVERNITR 244

Query: 241 SELMIADEVFLSGTAAKITPVKRIENFTLG-GDR-PITEKLRSVLTAVTENREPKYQDWV 298
            E+ IADE F +GTAA++TP++ ++N  +G G R PITE L++    V   R  K+ DW+
Sbjct: 245 DEVYIADEAFFTGTAAEVTPIRELDNREIGTGSRGPITELLQAKYFDVVHGRSSKHLDWL 304


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: 231
Number of extensions: 11
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: 308
Length adjustment: 27
Effective length of query: 278
Effective length of database: 281
Effective search space:    78118
Effective search space used:    78118
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.

Links

Downloads

Related tools

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