GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Frankia alni ACN14A

Align L-leucine transaminase; L-isoleucine transaminase (EC 2.6.1.42) (characterized)
to candidate WP_011606633.1 FRAAL_RS24185 PLP-dependent aminotransferase family protein

Query= reanno::acidovorax_3H11:Ac3H11_1358
         (401 letters)



>NCBI__GCF_000058485.1:WP_011606633.1
          Length = 484

 Score =  140 bits (353), Expect = 8e-38
 Identities = 110/361 (30%), Positives = 164/361 (45%), Gaps = 6/361 (1%)

Query: 37  GIISLAGGLPSPKTFPVSAFAAASAAVLANDGPAALQYAASEGYAPLRQAIADFLPWDVD 96
           G++ LA     P   PV   AAA+A       P A       G   LR  IA  +     
Sbjct: 126 GVLDLASAYLDPAAQPVGLLAAAAARAARR--PGAWDRTPVAGLPDLRGLIAGLVSPSHT 183

Query: 97  ADQILITTGSQQALDLIAKVLIDENSRVLVETPTYLGALQAFTPMEPSVVAVASDDEGVL 156
           A  +L+T+G Q AL L+ + L      + VE  TY GAL A        V V +D  GV 
Sbjct: 184 ASDVLVTSGGQAALALVFRALGRPGEALAVEHTTYPGALAAARAAGLVPVPVPADGAGVR 243

Query: 157 IDDLKAKVGTGADKARFLYVLPNFQNPTGRTMTEARRAALVKAAAELNLPLVEDNPYGDL 216
            DDL   +G     AR +Y+ P   NPTG  +   RR A++ A  +     VED+    L
Sbjct: 244 PDDLADVLGRSG--ARLVYLQPRHANPTGAVLAPDRRPAVLAALRDHRAFCVEDDWVAPL 301

Query: 217 WFDNPPPAPLTARNPEG-CIYMGSFSKVLAPGLRLGFVVAPKAVYPKLLQAKQAADLHTP 275
                 P PL A +P+G  +++ S SK ++PGLR+  V A   V  +L +A+   DL   
Sbjct: 302 DLTAVSPPPLAAADPDGHVVHVLSLSKSVSPGLRIAAVTARGPVAARLARARITDDLFVA 361

Query: 276 GYNQRLVAEVMKGNFLDRHVPTIRALYKQQCEAMLAALTQEMAGLGVEWNRPDGGMFLWV 335
              Q+   E++      RH+ ++R +   +  A+LAA+ + +  LG     P GG+ +W+
Sbjct: 362 PVLQQTAVELLSTPGWRRHLASLRRVLLARRAALLAAIARALPTLGPP-QPPSGGVHVWL 420

Query: 336 RLPEGMSAIELLPQAVERNVAFVPGAAFYADNADPRTLRLSFVTSTVEQIATGIAALAAA 395
            LP G     +   A    VA  PG+A+         LRL++  +  E +   +  LAA 
Sbjct: 421 PLPPGADDRLVTAAARRAGVAVGPGSAYTVGEVVAPHLRLTYSRTPGEGLVAAVDRLAAV 480

Query: 396 I 396
           +
Sbjct: 481 L 481


Lambda     K      H
   0.318    0.134    0.392 

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: 542
Number of extensions: 29
Number of successful extensions: 4
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: 401
Length of database: 484
Length adjustment: 32
Effective length of query: 369
Effective length of database: 452
Effective search space:   166788
Effective search space used:   166788
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: 51 (24.3 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