GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Acidimicrobium ferrooxidans DSM 10331

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate WP_015798122.1 AFER_RS03495 aromatic amino acid beta-eliminating lyase/threonine aldolase

Query= BRENDA::Q9X266
         (343 letters)



>NCBI__GCF_000023265.1:WP_015798122.1
          Length = 335

 Score =  231 bits (588), Expect = 3e-65
 Identities = 142/330 (43%), Positives = 189/330 (57%), Gaps = 6/330 (1%)

Query: 2   IDLRSDTVTKPTEEMRKAMAQAEVGDDVYGEDPTINELERLAAETFGKEAALFVPSGTMG 61
           IDLRSDTVT+PT+ MR+AMA A  GDD YGEDPT+ ELE  AA   G EAALFV SGTM 
Sbjct: 3   IDLRSDTVTQPTDAMRRAMASARCGDDGYGEDPTVRELEERAAGLLGMEAALFVASGTMA 62

Query: 62  NQVSIMAHTQRGDEVILEADSHIFWYEVGAMAVLSGVMPHPVPGKNGAMDPDDVRKAIRP 121
           NQV++   T  G  V++ A +H+  +E GA A  + V  H +   +GA   D V  A+  
Sbjct: 63  NQVALRTLTTPGSVVVVGARAHLCQFERGASARNALVQLHTLADDDGAPTADAVADAVAT 122

Query: 122 RNIHFPRTSLIAIENTHNRSGGRVVPLENIKEICTIAKEHGINVHIDGARIFNASIASGV 181
                 + +LIAIENTH  SGG   PL+ ++            ++IDGAR++NAS+A GV
Sbjct: 123 YRAIGVQPALIAIENTHMPSGG--TPLDPVRTGALADAATATPLYIDGARLWNASVALGV 180

Query: 182 PVKEYAGYADSVMFCLSKGLCAPVGSVVVGDRDFIERARKARKMLGGGMRQAGVLAAAGI 241
                   A +V  C SKGL AP+GSVV G  D +ERAR  R+ LGG +RQAG++AAA +
Sbjct: 181 EPSVLTERATAVSTCFSKGLGAPMGSVVAGSADLVERARWERQALGGRLRQAGIIAAAAL 240

Query: 242 IALTKMVDRLKEDHENARFLALKLKEIGYSVNPEDVKTNMVILRTDNLKVNAHGFIEALR 301
           +AL +    L  DHE A  L  ++             TNMV++  D         +  LR
Sbjct: 241 VALDEWRSVLARDHERAAVLRDRVAAELGDARVRWGGTNMVLVDAD----RPVEMLARLR 296

Query: 302 NSGVLANAVSDTEIRLVTHKDVSRNDIEEA 331
            +GVLANA+    +R V H+D+S  ++  A
Sbjct: 297 EAGVLANAIGPRTLRFVVHRDLSDAEVTVA 326


Lambda     K      H
   0.319    0.135    0.384 

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: 280
Number of extensions: 9
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: 343
Length of database: 335
Length adjustment: 28
Effective length of query: 315
Effective length of database: 307
Effective search space:    96705
Effective search space used:    96705
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 (21.7 bits)
S2: 49 (23.5 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