GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Methylovulum miyakonense HT12

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_019865509.1 METMI_RS0106730 aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_000384075.1:WP_019865509.1
          Length = 388

 Score =  240 bits (612), Expect = 6e-68
 Identities = 140/372 (37%), Positives = 195/372 (52%), Gaps = 3/372 (0%)

Query: 11  VPPFYVMDVWLAAAERQRTHGDLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGI 70
           + PFYVM +   A + +    D++++  G+P    P+ +  A    L   ++ Y+ A G+
Sbjct: 12  ISPFYVMALLQRAKQLESEGRDVIHMEIGEPDFPTPKAIVEAGVRLLQTGEVKYTPAAGL 71

Query: 71  PELRDAIAADYQRRHGITVEPDAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRN 130
            ELR  IA  YQ ++G++V P+ + IT G+SG FLLA     + G+ + MA P YPC  N
Sbjct: 72  LELRRKIARFYQSQYGVSVAPERIFITPGASGAFLLALGISLNPGEELLMADPCYPCNSN 131

Query: 131 ILSALGCEVVEIPCGPQTRFQPTA-QMLAEIDPPLRGVVVASPANPTGTVIPPEELAAIA 189
             S  G     +P    T +Q TA Q+        +GV+VASP+NPTGT+I PE L A+ 
Sbjct: 132 FASLFGATPRALPVDAGTSYQLTADQVKQHWHSHSKGVLVASPSNPTGTLISPEALQAVV 191

Query: 190 SWCDASDVRLISDEVYHGLVYQGAPQTSCAWQTSRNAVVVNSFSKYYAMTGWRLGWLLVP 249
              +A      SDE+YHGLVY      + A Q S    V+NSFSKY+ MTGWR+GWL+VP
Sbjct: 192 QTTNALGGCFYSDEIYHGLVY--GQNATTALQYSDEVFVINSFSKYFGMTGWRIGWLVVP 249

Query: 250 TVLRRAVDCLTGNFTICPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIG 309
                A + L  N  I     SQ AA++AF  E   E +   A  A  R  L   L  +G
Sbjct: 250 DGFISAAEKLAQNIFIATSTHSQYAALAAFDRETLVELERRRAELAARRDFLYAHLLDLG 309

Query: 310 IDRLAPTDGAFYVYADVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAG 369
               A  +GAFY+YAD S FT DS  F    L    VAI PG DF T      +R ++  
Sbjct: 310 FGIPAKPEGAFYIYADCSRFTDDSFQFALDFLEQEAVAITPGKDFGTYNAQHNLRFAYTT 369

Query: 370 PSGDIEEALRRI 381
            +  +  A++R+
Sbjct: 370 TADKMAAAMQRL 381


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: 15
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: 388
Length adjustment: 30
Effective length of query: 358
Effective length of database: 358
Effective search space:   128164
Effective search space used:   128164
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