GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Sphingomonas koreensis DSMZ 15582

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate Ga0059261_2301 Ga0059261_2301 homoserine O-acetyltransferase (EC 2.3.1.31)

Query= SwissProt::D2Z028
         (374 letters)



>FitnessBrowser__Korea:Ga0059261_2301
          Length = 371

 Score =  249 bits (635), Expect = 1e-70
 Identities = 144/363 (39%), Positives = 194/363 (53%), Gaps = 6/363 (1%)

Query: 9   SRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAAS-RPDDPT 67
           SR + LP    +  G  L    IAYET+G+L     NA+L+   L+ D H AS  P    
Sbjct: 10  SRHVTLPGPLRLDGGVLLSPVEIAYETYGTLAPDGGNAILICHALTGDQHVASPHPVTGK 69

Query: 68  PGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIA 127
           PGWW  MVGPGKPVD D   ++C N LGSC GS+GPA+ +P TG P+ + FP ++I D+ 
Sbjct: 70  PGWWTRMVGPGKPVDPDRHFIVCANVLGSCMGSSGPATVNPATGRPWGMDFPVITIRDMV 129

Query: 128 DAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRS 187
            A A  +  LG+ RL  VVG SMGGM AL+  A  P+     + ++        +IA   
Sbjct: 130 RAQAMLLDHLGVGRLKAVVGGSMGGMQALSWPATFPDRVDAVVVIASTARHSAQNIAFHE 189

Query: 188 LQREAIRSDPGWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRAD 247
           + R+A+ +DP W  G Y +G+ P  G+  AR    +TY S      +FGR    + R A 
Sbjct: 190 VGRQAVMADPRWNGGAYYDGDPPAAGLAVARMAAHITYLSEAGLTEKFGRRL--QAREAK 247

Query: 248 QGRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRMR 307
              F  +F++ESYL      F DRFD N+YLY++ AMD FDL +    GG    A    R
Sbjct: 248 SFGFDADFQIESYLRHQGLSFVDRFDANAYLYITRAMDYFDLAE--EHGGLLANAFRETR 305

Query: 308 VERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPVA 367
               LV    TD L+P    + I   L+A GA VSF+ + +P GHDAFL++       V 
Sbjct: 306 ARFCLV-SFDTDWLYPTRDSRAIVHALNAAGAPVSFVELSSPFGHDAFLLEAPELNRVVD 364

Query: 368 KFL 370
            FL
Sbjct: 365 GFL 367


Lambda     K      H
   0.321    0.138    0.427 

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: 475
Number of extensions: 26
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: 374
Length of database: 371
Length adjustment: 30
Effective length of query: 344
Effective length of database: 341
Effective search space:   117304
Effective search space used:   117304
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 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