GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysN in Sphingomonas indica Dd16

Align Aspartate aminotransferase; AAT; AspAT; Putative 2-aminoadipate transaminase; Transaminase A; EC 2.6.1.1; EC 2.6.1.39 (characterized)
to candidate WP_085217296.1 B9N75_RS02070 aminotransferase

Query= SwissProt::P58350
         (410 letters)



>NCBI__GCF_900177405.1:WP_085217296.1
          Length = 384

 Score =  177 bits (450), Expect = 4e-49
 Identities = 114/364 (31%), Positives = 192/364 (52%), Gaps = 16/364 (4%)

Query: 46  LGAGEPDFDTPEHVKQAASDAIHRGETKYTALDGTPELKKAIREKFQRENGLAYELDEIT 105
           LG G PDF  PE V   A++ +    ++Y  + G PEL+ A+ + + +  G+AY  DEIT
Sbjct: 28  LGQGFPDFGWPEDVVAKAAELLTGAASQYPPMRGLPELRAAVADHYSQHQGIAYAPDEIT 87

Query: 106 VATGAKQILFNAMMASLDPGDEVIIPTPYWTSYSDIVHICEGKPVLIACDASSGFRLTAE 165
           V +GA + L +A++A ++PGDEV++  P + +Y  +V    G P  +A      +R+T E
Sbjct: 88  VTSGATEALASALLALIEPGDEVLLFQPLYDAYVPMVRRGGGVPRYVALRPPE-WRITRE 146

Query: 166 KLEAAITPRTRWVLLNSPSNPSGAAYSAADYRPLLEVLLRHPHVWLLVDDMYEHIVYDGF 225
            +EAA+TPRTR V+ N+P NP+G A+S  +   L EV +    + +L D+++EH++  G 
Sbjct: 147 AIEAALTPRTRLVVFNNPHNPTGRAFSQDELTALAEVCVARDLI-VLSDEVWEHVMPGGA 205

Query: 226 RFVTPAQLEPGLKNRTLTVNGVSKAYAMTGWRIGYAGGPRELIKAMAVVQSQATSCPSSI 285
             +  A L PG+ +RT+ V    K +++TGW++G+   P  L   +       T      
Sbjct: 206 AHLPLASL-PGMSDRTVKVGSAGKIFSLTGWKVGWIAAPAALGDPITKAHQFVTFTTPPN 264

Query: 286 SQAASVAALNGPQDFLKERTESFQRRRDLVVNGLNAIDGLDCRVPEGAFYTFSGCAGVLG 345
            QAA    L   + + ++   +F   RD + +GL A  G      EG+++       +  
Sbjct: 265 LQAAVAYGLGKDEAYYRDMRAAFAVARDRLADGL-ADAGYVVLPGEGSYF-------LCV 316

Query: 346 KVTPSGKRIKTDTDFCAYLLEDAHVAVVPGSAF----GLSPFFRISYATSEAELKEALER 401
            +T SG     D  FC   + +A +A +P +AF     ++   R+ +A  +  + E L+R
Sbjct: 317 DLTASG-IAADDLTFCERAVREAGIAAIPLTAFFEETPVTNVIRLCFAKKQETIDEGLKR 375

Query: 402 IAAA 405
           +AAA
Sbjct: 376 LAAA 379


Lambda     K      H
   0.318    0.134    0.393 

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: 388
Number of extensions: 24
Number of successful extensions: 4
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: 410
Length of database: 384
Length adjustment: 31
Effective length of query: 379
Effective length of database: 353
Effective search space:   133787
Effective search space used:   133787
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 26 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