GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Xanthobacter autotrophicus Py2

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_012114576.1 XAUT_RS12870 branched-chain amino acid aminotransferase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000017645.1:WP_012114576.1
          Length = 297

 Score =  124 bits (312), Expect = 2e-33
 Identities = 93/287 (32%), Positives = 147/287 (51%), Gaps = 24/287 (8%)

Query: 9   YFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAK 68
           +++  FVP+ DAK+ V +H LHYG+  F G R        GTI  F+   H +RL  SA+
Sbjct: 16  WYDGVFVPWADAKLHVLSHGLHYGSTVFEGERAYG-----GTI--FKSAEHSERLRLSAE 68

Query: 69  FLHYDISAEKIKEVIVDFVKKNQPDKS----FYIRPLVY--SSGLGIAPRLHNLEKDFLV 122
            L + I    I E+  D  KK   +K+     YIRP+ +  S  +G+A + + +     V
Sbjct: 69  MLDFTIPYT-IGEI--DAAKKATLEKNNLVDAYIRPVAWRGSEMMGVAAQKNTIHLAIGV 125

Query: 123 YGLEMGDYLAAD----GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDE 178
           +  E   Y   +    G+   +S W R +  + P + K +  Y+   ++K  A   GF +
Sbjct: 126 W--EWPSYFDPEQRQKGLRLDLSEWRRPDPATIPCKAKAAGLYMICTISKHRAERRGFAD 183

Query: 179 AILMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPI 238
           A++++ +G V E TG NVF V++G I TP      L+G+TR +++ IA   G+   +R I
Sbjct: 184 ALMLDYRGYVAECTGANVFFVKDGVIHTP-TPDCFLDGLTRRTVIDIARRHGMEVVERHI 242

Query: 239 DKSELMIADEVFLSGTAAKITPVKRIENFTLGGDRPITEKLRSVLTA 285
              EL    E F++GTAA++TPV  I ++       IT +L    TA
Sbjct: 243 KPEELSSFTECFITGTAAEVTPVGSIADWHF-APSGITHQLMDSYTA 288


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: 223
Number of extensions: 14
Number of successful extensions: 3
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: 297
Length adjustment: 27
Effective length of query: 278
Effective length of database: 270
Effective search space:    75060
Effective search space used:    75060
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