GapMind for Amino acid biosynthesis

 

Alignments for a candidate for OAT in Sphingomonas wittichii RW1

Align Ornithine aminotransferase; OAT; EC 2.6.1.13; Ornithine--oxo-acid aminotransferase (uncharacterized)
to candidate WP_011952251.1 SWIT_RS07135 acetylornithine transaminase

Query= curated2:C3P3K3
         (396 letters)



>NCBI__GCF_000016765.1:WP_011952251.1
          Length = 396

 Score =  238 bits (608), Expect = 2e-67
 Identities = 141/372 (37%), Positives = 205/372 (55%), Gaps = 9/372 (2%)

Query: 28  KAEGVWVEDPEGNRYMDLLSAYSAVNQGHRHPKIINALIDQANRVTLTSRAFHSDQLGPW 87
           + EG ++    G RY+D  S  +    GH HP ++ A+ DQA  +  TS  + S Q   +
Sbjct: 19  RGEGCYLIGERGERYLDFASGIAVNILGHGHPDLVKAIADQAATLMHTSNLYGSPQGEAF 78

Query: 88  YEKVAKLTNKEMVLPMNTGAEAVETAIKTARRWAYDVKKVEANRAEIIVCEDNFHGRTMG 147
            +K+   T  + V   N+GAEAVE AIKTARR+ Y     E  R +II   + FHGRT+G
Sbjct: 79  AQKLVDKTFADTVFFTNSGAEAVECAIKTARRYHYVNGSPE--RTKIISFSNAFHGRTLG 136

Query: 148 AVSMSSNEEYKRGFGPMLPGIIVIPYGDLEALKAAITPNTAAFILEPIQGEAGINIPPAG 207
            +S +S  + + GF P+LPG  V+P+ DLEA +AA+   TA F++EP+QGE G+      
Sbjct: 137 TISATSQPKMRDGFEPLLPGFQVVPFNDLEAARAAVDATTAGFLVEPVQGEGGMTPSKPE 196

Query: 208 FLKEALEVCKKENVLFVADEIQTGLGRTGKVFACDWDNVTPDMYILGKALGGGVFPISCA 267
           FLK   ++C ++ +L + DE+Q G  RTG  FA +   +TPD+  + K + GG FP+   
Sbjct: 197 FLKGLRQICDEQGLLLILDEVQCGYCRTGTFFAHEQYGITPDIMAVAKGIAGG-FPLGAC 255

Query: 268 AANRDILGVFEPGSHGSTFGGNPLACAVSIAALEVLEEEKLTERSLQLGEKL---VGQLK 324
            A  +       G+HGST+GGNPLA A   A  +V   ++        G++L   + QL 
Sbjct: 256 LATEEAAKGMVFGTHGSTYGGNPLAMAAGEAVFKVAVNDEFLANVRATGDRLRQAIEQLI 315

Query: 325 EIDNPMITEVRGKGLFIGIELNE--PARPYCEQLK-AAGLLCKETHENVIRIAPPLVISE 381
              + +   VRG GL IGI+L +   AR +   L+   GLL     ENV+RI PPLVI E
Sbjct: 316 PNHDGVFDSVRGLGLMIGIKLKDAVEARAFVAHLRDHHGLLTVAAGENVVRILPPLVIEE 375

Query: 382 EDLEWAFQKIKA 393
             +    +K+ A
Sbjct: 376 SHIAECIEKLSA 387


Lambda     K      H
   0.317    0.136    0.402 

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: 13
Number of successful extensions: 5
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: 396
Length of database: 396
Length adjustment: 31
Effective length of query: 365
Effective length of database: 365
Effective search space:   133225
Effective search space used:   133225
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