GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Echinicola vietnamensis KMM 6221, DSM 17526

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate Echvi_0675 Echvi_0675 Aspartate/tyrosine/aromatic aminotransferase

Query= SwissProt::P96847
         (388 letters)



>FitnessBrowser__Cola:Echvi_0675
          Length = 400

 Score =  162 bits (409), Expect = 2e-44
 Identities = 118/365 (32%), Positives = 186/365 (50%), Gaps = 20/365 (5%)

Query: 32  DLVNLSAGQPSAGAPEPVRAAAAAALHLNQ-LGYSVALGIPELRDAIAADYQRRHGIT-V 89
           D+++LS G+P    P+ ++ AA AA+   +   YS   G  +LR+AIA   Q ++ I   
Sbjct: 33  DIISLSLGEPDFKTPQHIQDAAKAAIDEGKYFSYSPVAGYQDLREAIAQKLQTQNKINEA 92

Query: 90  EPDAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTR 149
           + + +V++TG+       F+   + GD V + SP +  Y  I+   G   V I    +  
Sbjct: 93  KAENIVLSTGAKHSIANIFMCLLNEGDEVVIFSPYWVSYAEIIKLAGGVPVLIEGTLENN 152

Query: 150 FQPTAQMLAE-IDPPLRGVVVASPANPTGTVIPPEELAAIASWCDA-SDVRLISDEVYHG 207
           F+ +A  L E I    + V+ +SP NPTG+V   EEL AIA       D+ +++DE+Y  
Sbjct: 153 FKASAAQLEEAITSKTKAVIYSSPCNPTGSVFSKEELEAIAEVIKKHQDIYVVADEIYEL 212

Query: 208 LVYQGAPQTSCAWQTSRN-AVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTIC 266
           + Y G   +  A     +  + VN FSK YAMTGWR+G++  P  + +A + + G FT  
Sbjct: 213 INYTGQHASMAALPGMFDRTITVNGFSKGYAMTGWRVGYICAPLFIAKACEKIQGQFTSG 272

Query: 267 PPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRI-GIDRLAPTDGAFYVYAD 325
              ++Q AA++A T + T   +   A Y   R L+L+ LR I GI    P +GAFY + D
Sbjct: 273 GTGIAQRAALAAITGDQTPSVEMEKA-YKKRRELVLELLRDIPGIKTHVP-EGAFYFFPD 330

Query: 326 VSDFTSDSLA---------FCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIEE 376
           V+ F   S           FC  +L    V++  G  F      + VR+S+A    +++E
Sbjct: 331 VTAFFGKSAGEVKVNNADDFCLYILNTAHVSVVTGAAFGAP---NCVRLSYAASEAELKE 387

Query: 377 ALRRI 381
           AL+RI
Sbjct: 388 ALKRI 392


Lambda     K      H
   0.321    0.136    0.416 

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: 348
Number of extensions: 25
Number of successful extensions: 7
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: 388
Length of database: 400
Length adjustment: 31
Effective length of query: 357
Effective length of database: 369
Effective search space:   131733
Effective search space used:   131733
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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