GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Desulfuromusa kysingii DSM 7343

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_092346870.1 BLU87_RS08685 pyridoxal phosphate-dependent aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_900107645.1:WP_092346870.1
          Length = 390

 Score =  157 bits (398), Expect = 4e-43
 Identities = 107/361 (29%), Positives = 179/361 (49%), Gaps = 7/361 (1%)

Query: 32  DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITVEP 91
           D+VNL  G+P    P  +  AA A++      YS   GI ELR A+A  Y ++    + P
Sbjct: 32  DVVNLCNGEPDFSTPSHICEAAIASIQGGDTRYSPTSGILELRQAVADKYTQQLKRRITP 91

Query: 92  DAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTRFQ 151
           D V+I  G +   +++ LA  + GD V +  P YP Y   +  +  + V IP   +  FQ
Sbjct: 92  DNVMIVCGGTEALMMSLLATVNPGDEVIVTDPCYPNYFAQIELVKAKCVSIPVYEKNNFQ 151

Query: 152 PTAQMLAE-IDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVRLISDEVYHGLVY 210
              + L + I    +G+++  P NP G     E + ++    D +++ + SDEVY  L Y
Sbjct: 152 IDPEDLKKAISSRTKGIILNYPNNPLGVTASEEYIQSLEQLIDDNNLIVFSDEVYESLTY 211

Query: 211 QGAPQTSCAWQTSR---NAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTICP 267
             +   S A Q  R   N +V+NS SK YAMTGWR+G+++    + +++  L  +   C 
Sbjct: 212 GKSGHYSLA-QNDRIKDNVLVMNSLSKTYAMTGWRIGYIVGHPKIMKSMFRLQESVLSCL 270

Query: 268 PVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAPTDGAFYVYADVS 327
           PV  Q AA++A    +  +     ++Y    +LL+DG++ +   +     G   V A++S
Sbjct: 271 PVFIQKAALAALR-GSQDKVQEMASAYEKRMNLLVDGIQSMPGFKCIRPMGGLCVMANIS 329

Query: 328 DFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIEEALRRIGSWLPS 387
            +   S  F  +LL + GV   PG  F    G  ++R  FA    +I++ + R+ S++ S
Sbjct: 330 AYNKSSEEFSRELLENAGVMTVPGSAFG-PMGEGYIRFCFANSFENIQKGVERLSSYIAS 388

Query: 388 Q 388
           +
Sbjct: 389 R 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: 338
Number of extensions: 16
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: 390
Length adjustment: 30
Effective length of query: 358
Effective length of database: 360
Effective search space:   128880
Effective search space used:   128880
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