GapMind for Amino acid biosynthesis

 

Alignments for a candidate for OAT in Paraburkholderia phymatum STM815

Align ornithine aminotransferase (EC 2.6.1.13) (characterized)
to candidate WP_012405496.1 BPHY_RS31375 aminotransferase class III-fold pyridoxal phosphate-dependent enzyme

Query= BRENDA::P31893
         (426 letters)



>NCBI__GCF_000020045.1:WP_012405496.1
          Length = 955

 Score =  142 bits (358), Expect = 4e-38
 Identities = 107/331 (32%), Positives = 159/331 (48%), Gaps = 22/331 (6%)

Query: 71  DMEGKRYFDFLSAYSAVNQGHCHPKIVNTMVEQAQ--RLTLTSRAFYTDVLGEYEEFLTK 128
           D  G+RY DF++ Y A+  GH HP  + + +E  +  R    ++       G   + L +
Sbjct: 123 DEHGERYLDFMAQYGALPFGH-HPAQIWSAIESLRDDREPNFAQPSLLKSAGALAQRLLE 181

Query: 129 LF--NYDKVLPMNTGVEGGETACKIARCWAYMKKKVPENQAKIIFAENNFWGRTLSAISA 186
           L     D V   N+G E  E A K+AR            +  ++   N+F G+T  A+SA
Sbjct: 182 LAPAGLDYVTFTNSGAESIEAALKMARH--------ATGRQAVLSTRNSFHGKTFGALSA 233

Query: 187 STDPMSYDELRPYMPGFEIVKYNDTAALEKAFQDPNV--CAYMVEPIQGEAGVVALDAGY 244
           +  P         + GF+ V+Y    +L +A +   V   A++VEPIQGE GV    AGY
Sbjct: 234 TGKPDYQVHFGLPLAGFDYVEYGCVDSLREALESGRVPYAAFVVEPIQGEGGVHVPPAGY 293

Query: 245 LTEVRELCTKYNVLFIADEVQTGLARTGRMLAVDHEDVKPDLLILGKALSGGLYPVSAVL 304
           L E   LC +  V+FI DEVQTGL RTG + A D ED++PD+L L KAL GGL P+ AVL
Sbjct: 294 LREAEALCRRNGVVFIVDEVQTGLGRTGALFACDDEDIRPDILTLSKALGGGLVPIGAVL 353

Query: 305 RDDHIMD---CIQPGLHTAMDVMDPRMRILAASRYYVRVARERCENAQIQATYLRKELNT 361
               +      ++     A + +  R   LA      R  R    + + +  YLR  L+T
Sbjct: 354 CSASVYTEKFALKHSSTFAGNALAARAG-LATLDLLTRDNRSLLAHVRTEGAYLRAGLDT 412

Query: 362 LP---KDVVPVVRGKGLLNAIVINKKFDAWD 389
           L     +++  VRG+G +  +        W+
Sbjct: 413 LQARHPNLIEQVRGRGFMLGLRFTTDRSEWN 443


Lambda     K      H
   0.322    0.137    0.424 

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: 785
Number of extensions: 43
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: 426
Length of database: 955
Length adjustment: 38
Effective length of query: 388
Effective length of database: 917
Effective search space:   355796
Effective search space used:   355796
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 (21.9 bits)
S2: 54 (25.4 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