GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Thauera aminoaromatica S2

Align L-leucine transaminase; L-isoleucine transaminase (EC 2.6.1.42) (characterized)
to candidate WP_004312947.1 C665_RS12800 PLP-dependent aminotransferase family protein

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



>NCBI__GCF_000310185.1:WP_004312947.1
          Length = 494

 Score =  131 bits (329), Expect = 5e-35
 Identities = 104/319 (32%), Positives = 149/319 (46%), Gaps = 20/319 (6%)

Query: 44  GLPSPKTFPVSAFAAASAAVLANDGPAALQYAASEGYAPLRQAIADFLP----WDVDADQ 99
           G+P    FP  A+ A       + G   L YAA  G   LR A+A  L       VDA Q
Sbjct: 126 GVPDFGAFPFRAWRACLERAWRDAGWRQLGYAAHGGDPSLRAALAAHLGSVRGLAVDAAQ 185

Query: 100 ILITTGSQQALDLIAKVLIDENSRVLVETPTYLGALQAFTPMEPSVVAVASDDEGVLIDD 159
           +LIT+G+Q  LDL A++L D    V VE P YL A  AF      V  V  DDEG+    
Sbjct: 186 LLITSGTQAGLDLCARLLADHGDTVWVENPGYLAARVAFGLAGLQVHDVMVDDEGL---- 241

Query: 160 LKAKVGTGADK-----ARFLYVLPNFQNPTGRTMTEARRAALVKAAAELNLPLVEDNPYG 214
                  GA+       R +   P+ Q P+GR M+  RR AL++ A      +VED+   
Sbjct: 242 -----APGAEDWLRHPPRLIMTTPSHQYPSGRVMSLPRRFALIERARAAGTWIVEDDYDS 296

Query: 215 DLWFDNPPPAPLTARNPEGCI-YMGSFSKVLAPGLRLGFVVAPKAVYPKLLQAKQAADLH 273
           +     P P  L    P   + Y G+FSK L PGLRLG++V P+ +    + A   A   
Sbjct: 297 EFRRAGPAPPALFGLQPGATVVYAGTFSKTLYPGLRLGYLVLPRTIAADFIHAAARATRA 356

Query: 274 TPGYNQRLVAEVMKGNFLDRHVPTIRALYKQQCEAMLAALTQEMAGLGVEWNRPDGGMFL 333
             G  QR +A+ +       H+  +RA Y  +  A+ AAL Q   G G+  +  + G+ L
Sbjct: 357 GQGIEQRALADFIGRGHYITHLRRMRARYNARQAALRAALRQAF-GPGLLLSGGEAGLHL 415

Query: 334 WVRLPEGMSAIELLPQAVE 352
            + LP+ +  + +  +A +
Sbjct: 416 VMWLPDELPDVAVAQRAAQ 434


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: 489
Number of extensions: 26
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: 494
Length adjustment: 32
Effective length of query: 369
Effective length of database: 462
Effective search space:   170478
Effective search space used:   170478
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