GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Roseburia faecis M72

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_055067282.1 M72_RS04030 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_001406815.1:WP_055067282.1
          Length = 390

 Score =  144 bits (364), Expect = 3e-39
 Identities = 110/361 (30%), Positives = 171/361 (47%), Gaps = 14/361 (3%)

Query: 32  DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITVEP 91
           D ++L  G+P    P  +R     +L   +  Y+   G+ EL+  I+    RR G++ + 
Sbjct: 29  DAISLGVGEPDFDTPWHIRDEGIYSLEKGRTFYTSNAGLKELKIEISRYLDRRFGLSYDY 88

Query: 92  DA-VVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTRF 150
           +  +++T G S    +A  A  D  D V +  P Y  Y           V I    +  F
Sbjct: 89  NKEMLVTVGGSEAIDIAMRAMLDPQDEVLIPQPSYVSYVPCCVLANGTPVPIELKAENEF 148

Query: 151 QPTAQML-AEIDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVRLISDEVYHGLV 209
           + TA+ L A I P  + +V+  P NPTG V+  ++L A+A      D+ ++SDE+Y  L 
Sbjct: 149 RLTAEELEAAITPKTKLLVMPFPNNPTGAVMEKKDLEAVAEVVKKHDLFVLSDEIYAELT 208

Query: 210 YQGAPQTSCAWQTSR-NAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTICPP 268
           Y     +  +    R   +V+N FSK +AMTGWRLG+   P V+ + +  +     +C P
Sbjct: 209 YLDNHVSIASIPGMRERTIVINGFSKSHAMTGWRLGYACGPEVIIKQMLKIHQFAIMCAP 268

Query: 269 VLSQIAAVSAFTPEATAEADGNLA----SYAINRSLLLDGLRRIGIDRLAPTDGAFYVYA 324
             SQ AAV     EA    D ++A     Y   R  +L+  + +G+    P  GAFY + 
Sbjct: 269 TTSQYAAV-----EALRNGDEDVAMMREEYNGRRRYVLERFKEMGLSCFEPF-GAFYAFP 322

Query: 325 DVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIEEALRRIGSW 384
            + D    S  F +KLL    VA+ PG  F  A G  F+RIS+A    D+  AL R+  +
Sbjct: 323 CIKDLGMTSDEFATKLLQTKKVAVVPGTAFG-ACGEGFLRISYAYSLDDLRIALDRVAEF 381

Query: 385 L 385
           +
Sbjct: 382 V 382


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: 342
Number of extensions: 22
Number of successful extensions: 6
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 Jul 25 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