GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Sphingomonas indica Dd16

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_085217296.1 B9N75_RS02070 aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_900177405.1:WP_085217296.1
          Length = 384

 Score =  148 bits (373), Expect = 3e-40
 Identities = 109/356 (30%), Positives = 164/356 (46%), Gaps = 9/356 (2%)

Query: 34  VNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITVEPDA 93
           VNL  G P  G PE V A AA  L      Y    G+PELR A+A  Y +  GI   PD 
Sbjct: 26  VNLGQGFPDFGWPEDVVAKAAELLTGAASQYPPMRGLPELRAAVADHYSQHQGIAYAPDE 85

Query: 94  VVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTRFQPT 153
           + +T+G++     A LA  + GD V +  P Y  Y  ++   G     +   P       
Sbjct: 86  ITVTSGATEALASALLALIEPGDEVLLFQPLYDAYVPMVRRGGGVPRYVALRPPEWRITR 145

Query: 154 AQMLAEIDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVRLISDEVYHGLVYQGA 213
             + A + P  R VV  +P NPTG     +EL A+A  C A D+ ++SDEV+  ++  GA
Sbjct: 146 EAIEAALTPRTRLVVFNNPHNPTGRAFSQDELTALAEVCVARDLIVLSDEVWEHVMPGGA 205

Query: 214 ---PQTSCAWQTSRNAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTICPPVL 270
              P  S    + R  V V S  K +++TGW++GW+  P  L   +       T   P  
Sbjct: 206 AHLPLASLPGMSDR-TVKVGSAGKIFSLTGWKVGWIAAPAALGDPITKAHQFVTFTTPPN 264

Query: 271 SQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAPTDGAFYVYADV--SD 328
            Q A       +     D   A++A+ R  L DGL   G   L P +G++++  D+  S 
Sbjct: 265 LQAAVAYGLGKDEAYYRDMR-AAFAVARDRLADGLADAGYVVL-PGEGSYFLCVDLTASG 322

Query: 329 FTSDSLAFCSKLLADTGVAIAP-GIDFDTARGGSFVRISFAGPSGDIEEALRRIGS 383
             +D L FC + + + G+A  P    F+     + +R+ FA     I+E L+R+ +
Sbjct: 323 IAADDLTFCERAVREAGIAAIPLTAFFEETPVTNVIRLCFAKKQETIDEGLKRLAA 378


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: 389
Number of extensions: 27
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: 384
Length adjustment: 30
Effective length of query: 358
Effective length of database: 354
Effective search space:   126732
Effective search space used:   126732
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 Jul 26 2024. The underlying query database was built on Jul 25 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