GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Caminibacter mediatlanticus TB-2

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_007474288.1 CMTB2_RS04230 aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_000170735.1:WP_007474288.1
          Length = 358

 Score =  220 bits (560), Expect = 6e-62
 Identities = 131/375 (34%), Positives = 212/375 (56%), Gaps = 24/375 (6%)

Query: 13  PFYVMDVWLAAAERQRTHGDLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPE 72
           PF VMD+      + +T  D+++L  G+P       V+ A+  A+  N+  Y+ + G+  
Sbjct: 3   PFIVMDI----VSKAKTIDDVIHLEIGEPDTLPSPKVKKASIKAIEENKFFYTESKGLKN 58

Query: 73  LRDAIAADYQRRHGITVEPDAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNIL 132
           LR+ IA  Y+  + + V+PD ++ITTG+S  FL+AF        ++A   PGYPCY+N  
Sbjct: 59  LREKIAKHYKIFYDVEVKPDNIIITTGTSTAFLIAFYFA----KKIATPIPGYPCYKNFA 114

Query: 133 SALGCEVVEIPCGPQTRFQPTAQMLAEIDPPLR--GVVVASPANPTGTVIPPEELAAIAS 190
                E V+IP    T F P  Q+  E    L+   ++++SP NPTGTVI  E L  I  
Sbjct: 115 ELENKEFVKIP----TSF-PDYQLTIEDLKKLKFDTLMISSPNNPTGTVIDKENLRKICE 169

Query: 191 WCDASDVRLISDEVYHGLVYQGAPQTSCAWQTSRNAVVVNSFSKYYAMTGWRLGWLLVPT 250
           +C  ++  LISDE+YHGLVY+   + + A + ++NA+++N FSK+++M G+R+GW+++P 
Sbjct: 170 FCKLNNKLLISDELYHGLVYE--KEYTTALKYNKNAIIINGFSKFFSMPGFRIGWIILPD 227

Query: 251 VLRRAVDCLTGNFTICPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGI 310
            L R  + +  N  I  P +SQ AA+ AF             ++   R  L   L+   I
Sbjct: 228 NLVRDAEVIAQNILISAPTISQYAAIEAFD---YGHLQNIQKTFKKRRDFLYKELK--DI 282

Query: 311 DRLAPTDGAFYVYADVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGP 370
             +A  DGAFY++ ++S ++ DSL+FC +LL  + VA  PGIDF   +  +F+RI++   
Sbjct: 283 FEIAKPDGAFYLWCNISKYSDDSLSFCDELLTKSKVATTPGIDFGDYK--NFIRIAYTKD 340

Query: 371 SGDIEEALRRIGSWL 385
              + EA++RI  ++
Sbjct: 341 ISILNEAVKRIKKFI 355


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: 301
Number of extensions: 12
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: 358
Length adjustment: 30
Effective length of query: 358
Effective length of database: 328
Effective search space:   117424
Effective search space used:   117424
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