GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Kyrpidia tusciae DSM 2912

Align Phosphoglycerate dehydrogenase (EC 1.1.1.95) (characterized)
to candidate WP_123809314.1 BTUS_RS12980 D-2-hydroxyacid dehydrogenase

Query= reanno::SB2B:6938941
         (308 letters)



>NCBI__GCF_000092905.1:WP_123809314.1
          Length = 421

 Score =  164 bits (415), Expect = 3e-45
 Identities = 107/309 (34%), Positives = 167/309 (54%), Gaps = 7/309 (2%)

Query: 7   LLTRENERYRSLLASCHLPELELLDDNPANIRLADIWLAEP-GLAAPLVNHASGLRWMQS 65
           L T+  ER + +     +  ++ L++   ++   ++ +     L    V     LRW+Q 
Sbjct: 113 LKTKHGERVKQVFPGVEIRTVQGLEEMGNDLAEIEVLITYGMDLDDRRVEEMKSLRWIQV 172

Query: 66  TFAGVDLL-VKPRQRRDYLLTNVRGIFGPLMSEYLFGYLLARQREHDLYKSQQQQKLWLP 124
             AGVD + +    RR  ++TN RG+ GP M+E+  G +L   R    +   Q++++W  
Sbjct: 173 FSAGVDRMPLATLDRRGIVVTNARGVHGPQMAEHALGIMLMHSRRLLEFARLQRERVWDR 232

Query: 125 G-SYKTLQGSELLLLGTGSIAKHLAQTAKHFGMKVAGINRSAKATEGFDEVAT-LEALPT 182
                 L G  L +LGTG+IA+ LA  ++  G+ V G NRS +A +GFD V +  + L  
Sbjct: 233 RIRVDELGGKVLGVLGTGAIAQDLATRSRALGLTVWGHNRSGRAVDGFDRVFSGKDGLDQ 292

Query: 183 LMARADAIASILPSTEATRGILNENILARMKPDAVLFNLGRGDVLDLDALERQLRQHPQQ 242
           L+A AD +  ++P T  TRG++ E  L RMK  A L N+ RG ++D  AL + L +    
Sbjct: 293 LLAGADYLVVLVPFTPQTRGMIGEAELRRMKSTAFLINMARGGIVDELALLQALTEGWIA 352

Query: 243 QAVLDVFNQEPLPEDHPIWGLGNVIVTPHIA--APSFPEQVAEIFSSNYHKFLLGE-TLS 299
            A LDVF QEPLP DHP WGL N ++TPH++  +P + ++  EIF  N   +L G     
Sbjct: 353 GAALDVFEQEPLPPDHPFWGLENCLLTPHVSGVSPYYNDRALEIFLRNLKVYLSGAGEWV 412

Query: 300 HRVNFERGY 308
           +RV+  +GY
Sbjct: 413 NRVDSRKGY 421


Lambda     K      H
   0.320    0.137    0.404 

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: 269
Number of extensions: 17
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: 308
Length of database: 421
Length adjustment: 29
Effective length of query: 279
Effective length of database: 392
Effective search space:   109368
Effective search space used:   109368
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: 49 (23.5 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