GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Trichlorobacter lovleyi SZ

Align Probable aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.78; Transaminase A (uncharacterized)
to candidate WP_012470645.1 GLOV_RS12865 pyridoxal phosphate-dependent aminotransferase

Query= curated2:O33822
         (383 letters)



>NCBI__GCF_000020385.1:WP_012470645.1
          Length = 397

 Score =  186 bits (471), Expect = 1e-51
 Identities = 128/350 (36%), Positives = 185/350 (52%), Gaps = 17/350 (4%)

Query: 37  TAGEPDFDTPEHVKEAGRRALAQ----GKTKYAPPAGIPELREAVAEKFRRENGLEVTPE 92
           T G PD + P+ +  A  + LAQ    G  +Y   AG PE R AVA K   ++GLEVT  
Sbjct: 40  TLGNPDVEPPQALHTALLQ-LAQHPLPGMHRYMNNAGYPETRAAVARKLAADSGLEVTAA 98

Query: 93  ETIVTVGGKQALFNLFQAILDPGDEVIVLAPYWVSYPEMVRFAGGVPVEVPTLPEEGFVP 152
             I+T G   AL  + + IL+PG+EVI+LAPY+V Y   +   GGVPVEV T   E F  
Sbjct: 99  HVIMTCGAGGALNVVLKTILNPGEEVIILAPYFVEYKFYIDNHGGVPVEVWT-NRETFRL 157

Query: 153 DPERVRRAITPRTKALVVNSPNNPTGVVYPEEVLRALAEMALQ------HDFYLVSDEIY 206
           D   +  AIT +T+A++VNSPNNPTGV+Y  E L AL E+  +      H  Y++SDE Y
Sbjct: 158 DLAAIEAAITTKTRAIIVNSPNNPTGVIYTAEELAALGELVKRAQARTGHQVYVISDEPY 217

Query: 207 EHLIYEGAHFSPGTLAPEHTITVNGAAKAFAMTGWRIGYACGPKAVIKAMADVSSQSTTS 266
             L Y+GA         E ++ V   +K  A+ G RIGY      +  AM  +  +    
Sbjct: 218 ARLSYDGAKVPNIFPLIESSVVVTSHSKDLALPGERIGYLAANPRMATAMQFM--EGAVF 275

Query: 267 PDTIAQWATLEALTNR-EASMAFIAMAREAYRKRRDLLLEGLSRIGLEAVRPSGAFYVLM 325
            +    +    AL  R  A +  +++    Y+ +RDL    L+ +G   V+P GAFY L 
Sbjct: 276 CNRTLGFVNAPALMQRLVADLQDVSVDSSLYQDKRDLFYTTLTGLGFSMVKPDGAFY-LF 334

Query: 326 DTSPFAPNEVEAAERLLMAGVAVVPGTEFAAFGHVRLSYATGEENLKKAL 375
             SPFA ++VE  +      + +VPG+ F A G+ R++Y      ++++L
Sbjct: 335 PKSPFA-DDVEFVKLAQKHHILLVPGSGFGAPGYFRIAYCVDRGMIERSL 383


Lambda     K      H
   0.317    0.133    0.382 

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: 361
Number of extensions: 18
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: 383
Length of database: 397
Length adjustment: 30
Effective length of query: 353
Effective length of database: 367
Effective search space:   129551
Effective search space used:   129551
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 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