GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Pseudomonas simiae WCS417

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate GFF3652 PS417_18690 aromatic amino acid aminotransferase

Query= BRENDA::W0PFQ7
         (399 letters)



>FitnessBrowser__WCS417:GFF3652
          Length = 398

 Score =  542 bits (1397), Expect = e-159
 Identities = 268/397 (67%), Positives = 318/397 (80%)

Query: 3   TLFNAVELAPRDPILGLNEQYNADTRDTKVNLGVGVYYDDNGKIPLLKAVQEAERQRVEA 62
           +LF+AVE+APRDPILGLNE +NADTR TKVNLGVGVY ++ GKIPLL+AV EAE  RV  
Sbjct: 2   SLFSAVEMAPRDPILGLNEAFNADTRTTKVNLGVGVYCNEEGKIPLLRAVAEAEAIRVAQ 61

Query: 63  HAARGYLPIEGIGNYNKGAQELLFGKDSDVITQGRALTFQALGGTGALKIGADFLKQLQP 122
           HAARGYLPI+GI  Y+K  Q LLFG +S ++   R  T QA+GGTGALK+GADFLKQL P
Sbjct: 62  HAARGYLPIDGIAAYDKAVQTLLFGAESPLLNADRVTTVQAVGGTGALKLGADFLKQLLP 121

Query: 123 DSTVYISDPSWENHRALFERAGFKVETYSYYDAATHGLNFDGFAASVKAMPEGSIIVLHA 182
           D+ V ISDPSWENHRALFE AGF V+ Y YYDAATH +N  G    + A+P  SI+VLHA
Sbjct: 122 DAVVAISDPSWENHRALFETAGFPVQNYRYYDAATHDVNRAGLLEDLNALPSQSIVVLHA 181

Query: 183 CCHNPTGVDPSPEQWQQIATLVKERNLVPFLDIAYQGFGAGLQEDAAVVRLFADLGMSMF 242
           CCHNPTGVD SP  WQ +  ++K +NLVPFLD+AYQGFG G+ EDAA VRLFA+ G++ F
Sbjct: 182 CCHNPTGVDLSPADWQNVLDVIKAKNLVPFLDMAYQGFGDGIHEDAAAVRLFAESGLTFF 241

Query: 243 ISSSFSKSFSLYGERVGALTVVTSSTDEASRVLSQIKRVIRTNYSNPPTHGGMVVAQILN 302
           +SSSFSKSFSLYGERVGAL++V  S +E++R+LSQ+KRVIRTNYSNPPTHG  +VA +LN
Sbjct: 242 VSSSFSKSFSLYGERVGALSIVGDSKEESARILSQVKRVIRTNYSNPPTHGAAIVAAVLN 301

Query: 303 TPELFAQWESELAQMRDRIREMRKQLTDKLNAAGVKQDFNFVMAQRGMFSYSGLTKEQVE 362
            PEL AQWE+ELA+MR RIR MR+Q+  +L  A    DF+FV  QRGMFSYSGLT EQV 
Sbjct: 302 NPELRAQWEAELAEMRLRIRGMREQMVAELAKAAPGHDFSFVGRQRGMFSYSGLTVEQVT 361

Query: 363 RLRTEHGIYAVNSGRICVAALNSRNIDSVVKAIAAVL 399
           RLR+E GIYA+++GRICVAALN  NID+V KAI  VL
Sbjct: 362 RLRSEFGIYALDTGRICVAALNQSNIDAVTKAIVQVL 398


Lambda     K      H
   0.318    0.134    0.385 

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: 478
Number of extensions: 16
Number of successful extensions: 1
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: 399
Length of database: 398
Length adjustment: 31
Effective length of query: 368
Effective length of database: 367
Effective search space:   135056
Effective search space used:   135056
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 09 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