GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Halorhodospira halophila SL1

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_049751641.1 HHAL_RS09970 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_000015585.1:WP_049751641.1
          Length = 399

 Score =  149 bits (376), Expect = 1e-40
 Identities = 111/360 (30%), Positives = 173/360 (48%), Gaps = 6/360 (1%)

Query: 32  DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITVEP 91
           D+++LS GQP    PE V  A   AL   + GY++  G+P++ +A+A  Y  R+   +EP
Sbjct: 41  DVIHLSIGQPDFPMPEHVVEAHIQALRDGKTGYTMDAGLPQMLEAVAEYYSHRYDRPLEP 100

Query: 92  DAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTRFQ 151
           + V+ITTG++    LA  A    G +  +  P +P Y  ++   G EV  IP   +   Q
Sbjct: 101 ENVLITTGATEAMYLAIAATAAPGRQFLIPDPTFPLYAPLIRMNGAEVKPIPTRAEHGHQ 160

Query: 152 PTAQ-MLAEIDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVRLISDEVYHGLVY 210
              Q ++  I     G+++ SP+NPTGTV P E + AI        V + SDEVY  L+ 
Sbjct: 161 IDPQEVIDNIGMRTFGIILNSPSNPTGTVYPRETIEAIVQEAAYRGVYVFSDEVYDHLLL 220

Query: 211 QGAPQTSCAWQTS--RNAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTICPP 268
                 S    TS   + + V+S SK ++M G R+GWL+      + +       T    
Sbjct: 221 DEMEYPSVLRCTSDLDHVMAVSSLSKTFSMAGLRIGWLISSQGAIKKLQRFHIFTTTVAN 280

Query: 269 VLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAPTDGAFYVYADVSD 328
             +Q A V+A      A  D  L +Y   R  +++ + +          GAFY++  +  
Sbjct: 281 TPAQWAGVAAL-KGGMACVDEMLEAYRQRRDRIVELVSKTPHLTSYRPQGAFYIFPSLPP 339

Query: 329 FTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIEEALRRIGSWLPSQ 388
            T D+    +++L +TGV + PG  F  +   S +RIS+A    DIE A  RI  W+  Q
Sbjct: 340 NT-DATNLATRMLKETGVCVVPGDAFGDSCPNS-LRISYAASMDDIERAFERIIPWMEKQ 397


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: 382
Number of extensions: 18
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: 399
Length adjustment: 31
Effective length of query: 357
Effective length of database: 368
Effective search space:   131376
Effective search space used:   131376
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 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

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