GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Chlorobaculum tepidum TLS

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate NP_661505.1 CT0605 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_000006985.1:NP_661505.1
          Length = 356

 Score =  241 bits (614), Expect = 3e-68
 Identities = 137/352 (38%), Positives = 198/352 (56%), Gaps = 23/352 (6%)

Query: 28  SEPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWD 87
           +EPL L+ G  LP   + Y T+G LN E SN +L+CHAL+G+       A+ D    WW 
Sbjct: 20  NEPLQLELGGELPGVRVAYRTWGTLNAEKSNVILVCHALTGN-------ADAD---SWWC 69

Query: 88  SAIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYR 147
              G G+  D  R F+VC N LG C G+TGP+SV+P SG+ YGPDFP +T++D V+ Q  
Sbjct: 70  GMFGEGRAFDETRDFIVCSNVLGSCYGTTGPMSVNPLSGRHYGPDFPRITIRDMVNVQRL 129

Query: 148 LMQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQA 207
           L++ LG+     ++G SLGGMQVL+W   YP+     + +  + R SA  IA +E  RQA
Sbjct: 130 LLRSLGIDRIRLIVGASLGGMQVLEWGAMYPEMAGALMPMGVSGRHSAWCIAQSEAQRQA 189

Query: 208 IITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELRAGQVQYGFDVE 267
           I  D E+  G Y D    PR+GL  ARM+   TY   +  + +FGR+ R        D  
Sbjct: 190 IAADAEWQDGWY-DPEVQPRKGLAAARMMAMCTYRCFENYQQRFGRKQRE-------DGL 241

Query: 268 FQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVAALAEVKAHFLVVSFT 327
           F+ ESY+R+QG   V RFDANTY+ +T+A+D  D  +   D   AAL  +K    ++S  
Sbjct: 242 FEAESYVRHQGDKLVGRFDANTYITLTRAMDMHDLGR-GRDSYEAALGALKMPVEILSID 300

Query: 328 SDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLAGY 379
           SD  +  +   E+ R  L  G ++ +  ++  +GHDAFL+      R++  +
Sbjct: 301 SDVLYPRQEQEELAR--LIPGSRLLF--LDEPYGHDAFLIDTETVSRMVCEF 348


Lambda     K      H
   0.320    0.135    0.412 

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: 396
Number of extensions: 18
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: 403
Length of database: 356
Length adjustment: 30
Effective length of query: 373
Effective length of database: 326
Effective search space:   121598
Effective search space used:   121598
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 (21.8 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