GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Nitratifractor salsuginis DSM 16511

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate WP_013554875.1 NITSA_RS09790 alanine--glyoxylate aminotransferase family protein

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000186245.1:WP_013554875.1
          Length = 377

 Score =  192 bits (487), Expect = 2e-53
 Identities = 133/373 (35%), Positives = 203/373 (54%), Gaps = 18/373 (4%)

Query: 6   MLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLTTSGTG 65
           +L  PGPTPVPE V LAMA   + HR+ +F  I A     L  L  T+ +V+ML +SGTG
Sbjct: 2   LLFTPGPTPVPESVRLAMAGPTLHHRTPEFEAIFAVARTKLFELMVTD-EVVMLASSGTG 60

Query: 66  AMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDFKTLLE 125
           AMEA++ N      ++L  N GKFG R+  +A+  GL   EI  EW       +   +L 
Sbjct: 61  AMEAAVTNLCHR--KLLNVNAGKFGQRFGLIAQAHGLPHTEIVHEWDTPATVGEVMEILR 118

Query: 126 ADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGGALMIV-DAVTSLGATPVAIDDLG 184
           +DS+  I AL I  SE++ G+ + +  I AA KA    +M++ D +T++G     ID   
Sbjct: 119 SDSE--IDALAIQISESAGGLRHPVEEIAAAVKAERPEVMVIADGITAVGVE--RIDTSN 174

Query: 185 LDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSPFTPP 244
           +D + +GSQK  M+PPGL  + +S  A +         +Y +L    K   ++++ +T P
Sbjct: 175 IDALIAGSQKALMLPPGLAILGLSNVAVEKIGNGR--GYYFNLASEIKKQRQNTTAYTAP 232

Query: 245 INLMYGLQASLQMMKAEG-LDAIFTRHQRHTNATRGAMKALNLPLFAPDNAASNAITAVA 303
             L+ GL+A L+ ++ +G L  ++    R   ATR A++AL L  + P   A +  T   
Sbjct: 233 TTLIIGLKAILEEIEKQGGLGKLYCDTARRAKATRFALEALGLHSY-PKTPARSMTTIDD 291

Query: 304 PLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATLIEL 363
           P   +A  IRS ++  F + +AGGQDHLKGKIFRI  +G +   +++  + A+E  L ++
Sbjct: 292 P---DANTIRSLLKSDFGVNVAGGQDHLKGKIFRINQMGLIEPHEMVWVVNAVELALAKM 348

Query: 364 GYEGVTPGSGVAA 376
           G     P  G AA
Sbjct: 349 GRR---PFDGTAA 358


Lambda     K      H
   0.317    0.134    0.386 

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: 312
Number of extensions: 18
Number of successful extensions: 7
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: 384
Length of database: 377
Length adjustment: 30
Effective length of query: 354
Effective length of database: 347
Effective search space:   122838
Effective search space used:   122838
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 Apr 09 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