GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Hydrogenovibrio kuenenii DSM 12350

Align phosphoserine aminotransferase monomer (EC 2.6.1.1; EC 2.6.1.52) (characterized)
to candidate WP_024851959.1 N745_RS0109870 alanine--glyoxylate aminotransferase family protein

Query= metacyc::MONOMER-15919
         (385 letters)



>NCBI__GCF_000526715.1:WP_024851959.1
          Length = 371

 Score =  228 bits (581), Expect = 2e-64
 Identities = 134/363 (36%), Positives = 205/363 (56%), Gaps = 7/363 (1%)

Query: 8   KLLMIPGPTMVPPEVLNAMALPVIGHRTKDYSNLLEDTIEKLKKVFITEND-TFLITGSG 66
           + LM PGP+ V P +L+AMA P IGH    +  ++++    LK  F TEN+ T  ++  G
Sbjct: 9   RTLMGPGPSDVHPRILSAMARPTIGHLDPAFVGMMDEVKAMLKYAFQTENEMTMPVSAPG 68

Query: 67  TAAMDMAISNIIKRGDKVLNIVTGNFGERFANIVKAYKGEAIRLDVEWGDMAEPEAVKEI 126
           +A M+   +N+++ GDKV+  + G FG R    V+   G  + ++ +WG     E V E 
Sbjct: 69  SAGMETCFANLVEPGDKVVVCINGVFGMRMKENVERAGGICVEVNDDWGKAVSAEKVDET 128

Query: 127 LDKYDDIKAVTVVHNETSTGARNPIKEIGEVVKDYDALYIVDTVSSLGGDYVNVDKFHID 186
           L    D K +  VH ETSTGA +  K + E+ + +D L IVD V+SLGG  + VD++ ID
Sbjct: 129 LAANPDAKILAFVHAETSTGACSDAKTLCEIARKHDCLSIVDAVTSLGGVELRVDEWGID 188

Query: 187 ICVTGSQKCLAAPPGLAAITVSEKAWEVIKKNDDKV-GFYLDLLAYKKYYEE--KKQTPY 243
              +G+QKCL+  PGL+ ++ SEKA + ++    KV  ++LDL     Y+ +  K+   +
Sbjct: 189 AIYSGTQKCLSCTPGLSPVSFSEKALDKVRNRKTKVQSWFLDLNLVMGYWGQGTKRAYHH 248

Query: 244 TPSVNLTYALNVALDLVLEEGIENRVKRHERLAKATRAGLEAMGIELFAKERARSVTVTS 303
           T  +N  YAL+ +L ++ EEG+EN   RH+ +    + GLE MGI     E  R   + S
Sbjct: 249 TAPINALYALHESLLMLQEEGLENAWARHKAMHDKLKVGLEEMGIGFVVDESVRLPQLNS 308

Query: 304 AKYPEGIEDSKFRGILSNKYNIVVAGGQKHLAGKIFRIGHMGICGEKEVLATLACVELAL 363
              PEG++D+  R  L N YN+ +  G    AGK++RIG MG   ++E    L CV  AL
Sbjct: 309 VWIPEGVDDAAVRSELLNTYNLEIGAGLGDFAGKVWRIGLMGFSAKEE--NVLFCVS-AL 365

Query: 364 KEL 366
           K++
Sbjct: 366 KKV 368


Lambda     K      H
   0.316    0.135    0.379 

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: 351
Number of extensions: 14
Number of successful extensions: 3
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: 385
Length of database: 371
Length adjustment: 30
Effective length of query: 355
Effective length of database: 341
Effective search space:   121055
Effective search space used:   121055
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 (21.6 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