GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Stenotrophomonas chelatiphaga DSM 21508

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_057506846.1 ABB28_RS01035 pyridoxal phosphate-dependent aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_001431535.1:WP_057506846.1
          Length = 382

 Score =  134 bits (338), Expect = 3e-36
 Identities = 108/361 (29%), Positives = 159/361 (44%), Gaps = 15/361 (4%)

Query: 30  HGDLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITV 89
           HG  VNL  G P   AP+ +  A  AA+      Y    G+  LR AIA      +G  V
Sbjct: 25  HG-AVNLGQGFPDFSAPQRLIDATTAAMADGLNQYPPMTGVAPLRQAIAQKSLDLYGAQV 83

Query: 90  EPDA-VVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQT 148
           +PD  + +T+G++     A  A   AG+ V +  P Y CY   +   G   V +P  PQT
Sbjct: 84  DPDTEITVTSGATEAIFNAIHAVVRAGEEVIVLDPAYDCYEPAIDLAGARAVHVPLDPQT 143

Query: 149 RFQPTAQMLAEIDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVRLISDEVYHGL 208
                 ++ A I P  R ++V +P NP+G ++   +L A+A     +D+ LISDEVY  +
Sbjct: 144 FAVDWDRVRAAITPRTRLLMVNTPHNPSGAMLAEADLQALADLLRGTDIYLISDEVYEHI 203

Query: 209 VYQGAPQTSCAW--QTSRNAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCL--TGNFT 264
           +Y G    S     +    A V++SF K Y  TGW++G+ + P  L      +     FT
Sbjct: 204 IYDGRRHESALRHPELRARAFVISSFGKTYHCTGWKIGYAIAPPALSAEFRKVHQYNTFT 263

Query: 265 ICPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAPTDGAFYV-- 322
              P     AA+    P+   E     A Y   R    + L +  +  LA   G F +  
Sbjct: 264 SFGPAQYGFAAMIRDEPQHHLELG---AFYQAKRDRFREQLAQTRLVPLAVPGGYFQLVD 320

Query: 323 YADVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTAR--GGSFVRISFAGPSGDIEEALRR 380
           Y+ +SD       F   L  + GVA  P   F  A   G   VR+ FA     ++ A+ R
Sbjct: 321 YSAISDLPDHE--FVKWLTIEKGVAAIPLSPFYEAPPVGQRIVRLCFAKNEATLDAAIER 378

Query: 381 I 381
           +
Sbjct: 379 L 379


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: 369
Number of extensions: 20
Number of successful extensions: 3
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: 382
Length adjustment: 30
Effective length of query: 358
Effective length of database: 352
Effective search space:   126016
Effective search space used:   126016
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 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