GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Synechococcus elongatus PCC 7942

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate Synpcc7942_2545 Synpcc7942_2545 aspartate aminotransferase

Query= SwissProt::P96847
         (388 letters)



>FitnessBrowser__SynE:Synpcc7942_2545
          Length = 392

 Score =  171 bits (432), Expect = 4e-47
 Identities = 119/366 (32%), Positives = 182/366 (49%), Gaps = 11/366 (3%)

Query: 22  AAAERQRTHG-DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAAD 80
           A A+  +  G D+ + SAG+P    P  +R AAA AL   +  Y  A G P+LR+AIA  
Sbjct: 20  AQAKAMKAEGLDVCSFSAGEPDFETPLHIRNAAAQALAEGKTRYGPAAGEPDLREAIAQK 79

Query: 81  YQRRHGITVEPDAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALG--CE 138
            +  +G+  +   +++T G             D GD V + +P +  Y  ++   G    
Sbjct: 80  LRADNGLDYQAANILVTNGGKQSLYNLMQVLLDPGDEVIIPAPYWLSYPEMVKLAGGVPV 139

Query: 139 VVEIPCGPQTRFQPTAQMLAEIDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVR 198
           +VE       + QP  Q+   I P  R +V+ SP+NPTG V   +EL AIA   +A D  
Sbjct: 140 IVETFASDGFKLQP-QQLAGAITPRTRLLVLNSPSNPTGMVYSRQELEAIAPIIEAHDFW 198

Query: 199 LISDEVYHGLVYQGAPQTSCAWQTS---RNAVVVNSFSKYYAMTGWRLGWLLVPTVLRRA 255
           ++SDE+Y  ++Y GA   S    +       ++ N F+K Y+MTGWR+G+L  P+ L  A
Sbjct: 199 VVSDEIYEKILYDGADHHSIGSLSPACFERTLISNGFAKAYSMTGWRVGYLAGPSELIAA 258

Query: 256 VDCLTGNFTICPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAP 315
              L  + T      +Q  A++A        A+  LA++   R L+L+GL +I       
Sbjct: 259 AASLQSHSTSNVCTFAQYGAIAALQGPQDCVAE-MLAAFTERRQLILNGLNQIAGLSCPI 317

Query: 316 TDGAFYVYADVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIE 375
            +GAFYV+ D+S    DS+ +C +LL    VA  PGI F   R    +R+S+A     IE
Sbjct: 318 PEGAFYVFVDISKTGLDSMTYCRQLLDQHQVAAIPGIAFGDDRS---IRLSYATDCQTIE 374

Query: 376 EALRRI 381
           + L R+
Sbjct: 375 KGLERL 380


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: 402
Number of extensions: 23
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: 388
Length of database: 392
Length adjustment: 31
Effective length of query: 357
Effective length of database: 361
Effective search space:   128877
Effective search space used:   128877
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