GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Clostridium acetobutylicum ATCC 824

Align phosphoserine aminotransferase monomer (EC 2.6.1.1; EC 2.6.1.52) (characterized)
to candidate NP_346862.1 CA_C0221 aspartate aminotransferase

Query= metacyc::MONOMER-15919
         (385 letters)



>NCBI__GCF_000008765.1:NP_346862.1
          Length = 377

 Score =  221 bits (562), Expect = 3e-62
 Identities = 132/375 (35%), Positives = 211/375 (56%), Gaps = 7/375 (1%)

Query: 9   LLMIPGPTMVPPEVLNAMALPVIG-HRTKDYSNLLEDTIEKLKKVFITENDTFLITGSGT 67
           ++M PGPT V   V  + A          D+ +  + T EK+ K   T+N+  +++G G 
Sbjct: 5   IIMTPGPTSVRENVRLSRAEKTTNPDLDMDFYDFYKKTTEKIGKFLKTKNEVRILSGEGI 64

Query: 68  AAMDMAISNIIKRGDKVLNIVTGNFGERFANIVKAYKGEAIRLDVEWGDMAEPEAVKEIL 127
             ++ A +++ ++GD+VL I  G FGE FA+ VK Y GE              E ++  L
Sbjct: 65  LGLEAACASLTEKGDRVLVIENGIFGEGFADFVKMYGGEPFFFRGNKKCSINIEELERFL 124

Query: 128 DKYDDIKAVTVVHNETSTGARNPIKEIGEVVKDYDALYIVDTVSSLGGDYVNVDKFHIDI 187
           D   + K  TVVH +T +G  N +  I +++K    + +VD+VS++GG+ + VD++ IDI
Sbjct: 125 DSDSEFKYATVVHCDTPSGMLNNVGAICKLLKKKGIMTVVDSVSAMGGEELKVDEWDIDI 184

Query: 188 CVTGSQKCLAAPPGLAAITVSEKAWEVIKKNDDKV-GFYLDLLAYKKYYEEKKQTPYTPS 246
            + GSQKC++APPGL  +++S+ A+  +K     +  FY +LL ++ YY  KK  PYTP 
Sbjct: 185 VIGGSQKCISAPPGLTIVSISDDAFSAMKNRKTPIASFYCNLLVWEDYY-NKKWFPYTPP 243

Query: 247 VNLTYALNVALDLVLEEGIENRVKRHERLAKATRAGLEAMGIELFAKERARSVTVTSAKY 306
           ++   AL  A++ +LEE  ++ + RH+++A ATRA +   G+E++  E   S TVT  K 
Sbjct: 244 ISDIVALRKAVENILEE--KDIIARHDKIASATRAAVVLGGLEIYI-EDGFSNTVTVIKV 300

Query: 307 PEGIEDSKFRGILSNKYNIVVAGGQKHLAGKIFRIGHMG-ICGEKEVLATLACVELALKE 365
           P G+ D K    +   YN+++AG   +L GK+ RIGHMG      +V  TL  ++  L+ 
Sbjct: 301 PHGMNDDKILSYMKENYNVMIAGAFDYLKGKVLRIGHMGENAYVDKVSYTLFALQRTLEH 360

Query: 366 LGFEVKESGVEVAKE 380
            GFE K   V+V  E
Sbjct: 361 YGFEFKRDMVKVFLE 375


Lambda     K      H
   0.316    0.135    0.379 

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: 370
Number of extensions: 21
Number of successful extensions: 5
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: 385
Length of database: 377
Length adjustment: 30
Effective length of query: 355
Effective length of database: 347
Effective search space:   123185
Effective search space used:   123185
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 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