GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pelobacter propionicus DSM 2379

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate WP_011734975.1 PPRO_RS05105 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>NCBI__GCF_000015045.1:WP_011734975.1
          Length = 398

 Score =  178 bits (451), Expect = 3e-49
 Identities = 132/369 (35%), Positives = 195/369 (52%), Gaps = 23/369 (6%)

Query: 26  LRRQGVD--LVALTAGEPDFDTPEHVKE---AARRALAQGKTKYAPPAGIPELREALAEK 80
           LRR+  D  +   T G PD + P+  +E   A  R    G  +Y   AG PE R A+A K
Sbjct: 27  LRREFGDESVYDFTLGNPDVEPPQAFQEELLALARNPLPGMHRYMNNAGYPETRAAVAAK 86

Query: 81  FRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGVVV 140
             R++G+ +T E  I+T G   AL  + + IL+PG+EVI+L+PY+V Y   +   GGV V
Sbjct: 87  LARDSGIDLTAEHVIMTCGAGGALNVVLKTILNPGEEVIILAPYFVEYKFYIDNHGGVPV 146

Query: 141 EVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVE----- 195
            V T   + F  D E + +AIT +T+A+++ SPNNPTG +YP E L  L  +  +     
Sbjct: 147 PVWT-DHQTFQLDIEAIEQAITLKTRAILICSPNNPTGVIYPAESLARLGEVVKKVHKRN 205

Query: 196 -HDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMTGWRIGY-ACGPK--E 251
            H  Y++SDE Y  + Y+G+         E ++ V   +K  A+ G RIGY A  P+   
Sbjct: 206 GHLIYVISDEPYARIAYDGKQVPNIFPLIESSVIVTSHSKDLALPGERIGYLAANPRMDT 265

Query: 252 VIKAMASVSSQSTTSPDTIAQWATLEALTN-QEASRAFVEMAREAYRRRRDLLLEGLTAL 310
           V++ MA     +       A       +TN Q+ S   V++A  AY+ +RDLL+  LTAL
Sbjct: 266 VMQFMAGAVFSNRVLGFVNAPALMQRLVTNLQDES---VDIA--AYQDKRDLLVRELTAL 320

Query: 311 GLKAVRPSGAFYVLMDTSPIAPDEVRAAERLLEAGVAVVPGTDFAAFGHVRLSYATSEEN 370
           G K V P GAFY L   SP+A D+V   +   +  + +VPG  F A G  R++Y      
Sbjct: 321 GFKMVIPDGAFY-LFPQSPLA-DDVAFVKLAQKHHILLVPGAGFGAPGFFRIAYCVDRAV 378

Query: 371 LRKALERFA 379
           + ++L  +A
Sbjct: 379 IERSLPAWA 387


Lambda     K      H
   0.317    0.133    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: 376
Number of extensions: 20
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: 398
Length adjustment: 31
Effective length of query: 354
Effective length of database: 367
Effective search space:   129918
Effective search space used:   129918
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 (21.7 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