GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Bacteroides thetaiotaomicron VPI-5482

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate 351943 BT2415 aspartate aminotransferase (NCBI ptt file)

Query= SwissProt::P96847
         (388 letters)



>FitnessBrowser__Btheta:351943
          Length = 397

 Score =  147 bits (370), Expect = 7e-40
 Identities = 112/366 (30%), Positives = 176/366 (48%), Gaps = 24/366 (6%)

Query: 32  DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITVEP 91
           D++NLS G+P    P+ ++ AA  A+  N   YS   G P LR+AI    ++ +G+    
Sbjct: 32  DVINLSVGEPDFNTPDHIKEAAKKAIDDNFSRYSPVPGYPALRNAIVEKLKKENGLEYTA 91

Query: 92  DAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTRFQ 151
             +    G+      A L   + GD V + +P +  Y  ++       V +  G +  F+
Sbjct: 92  AQISCANGAKQSVCNAILVLVNPGDEVIVPAPYWVSYPEMVKMAEGTPVIVSAGIEQDFK 151

Query: 152 PTAQML-AEIDPPLRGVVVASPANPTGTVIPPEELAAIAS-WCDASDVRLISDEVYHGLV 209
            T + L A I P  + +++ SP+NPTG+V   EELA +A+       V +I+DE+Y  + 
Sbjct: 152 ITPKQLEAAITPKTKALILCSPSNPTGSVYSKEELAGLAAVLAKYPQVVVIADEIYEHIN 211

Query: 210 YQGAPQTSCAW-QTSRNAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTICPP 268
           Y GA Q+   + +     V+VN  SK YAMTGWR+G++  P  + +A + L G +T  P 
Sbjct: 212 YIGAHQSIAQFPEMKERTVIVNGVSKAYAMTGWRIGFIAGPEWIVKACNKLQGQYTSGPC 271

Query: 269 VLSQIAAVSAF--TPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAPTDGAFYVYADV 326
            +SQ AA +A+  T E   E      ++   R L++   + +    +    GAFY++   
Sbjct: 272 SVSQKAAEAAYVGTQEPVKEMQ---KAFERRRDLIVKLAKEVPGFEVNVPQGAFYLFPKC 328

Query: 327 SDF-----------TSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIE 375
           S F            SD LA    LL D  VA   G  F        +R+S+A    +I 
Sbjct: 329 SYFFGKSNGERKIENSDDLAM--YLLEDAHVACVGGTSFGAP---ECIRMSYATSDENIV 383

Query: 376 EALRRI 381
           EA+RRI
Sbjct: 384 EAIRRI 389


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: 364
Number of extensions: 22
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: 388
Length of database: 397
Length adjustment: 31
Effective length of query: 357
Effective length of database: 366
Effective search space:   130662
Effective search space used:   130662
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