GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Prosthecochloris aestuarii DSM 271

Align serine O-acetyltransferase (EC 2.3.1.30) (characterized)
to candidate WP_012505314.1 PAES_RS03660 homoserine O-acetyltransferase

Query= BRENDA::I1R9N5
         (509 letters)



>NCBI__GCF_000020625.1:WP_012505314.1
          Length = 357

 Score =  207 bits (528), Expect = 4e-58
 Identities = 111/273 (40%), Positives = 155/273 (56%), Gaps = 15/273 (5%)

Query: 95  KEPFLLDWGGILPEFNIAYETWGELNADKSNAILLHTGLSASSHAHSTETNPKPGWWEKF 154
           ++PF L+ GG+LPE  +AY TWG LN D+SNA+L+   L+ S+ A          WW   
Sbjct: 17  RQPFTLESGGVLPEVTVAYRTWGRLNRDRSNAVLVCHALTGSADADE--------WWPGM 68

Query: 155 IGPGGPLDTNKYHVICTNVIGGCNGSTGPSSVDPGNGERYATRFPILTMDDMVRAQFKLL 214
            G G   D +   VIC+NV+G C G+TGP SV+P +G  Y   FP +T+ DMV  Q  LL
Sbjct: 69  FGKGCAFDPDHDFVICSNVLGSCYGTTGPLSVNPQSGRHYGPDFPAITIRDMVHLQRLLL 128

Query: 215 DHLGIDKLYASVGSSMGGMQSLAAGVQSPSRVGRIVSISGCARSHPYSIAMRHTQRQVLM 274
           D LGI++L   VG+S+GGMQ L  G   P +V  ++ +    R   + IA    QR  +M
Sbjct: 129 DELGIERLRLVVGASLGGMQVLEWGCLYPEKVHALMPMGISGRHSAWCIAQSEAQRSAIM 188

Query: 275 MDPNWNRGFYYGKVPPHAGMKLAREIATVTYRSGPEWEQRFGRRRADSSKPPALCPDFLI 334
            D  WN G+Y     P  G+  AR +A  TYRS   +++RFGR+R DS         F  
Sbjct: 189 ADREWNDGWYDPAHQPKGGLGAARMMAMCTYRSFENFQERFGRKRKDSLL-------FQA 241

Query: 335 ETYLDHAGEKWCLNYDPNSLLYVSKAMDLFDLG 367
           E+YL + GEK    +D N+ + +++AMD+ DLG
Sbjct: 242 ESYLHYQGEKLVRRFDANTYIALTRAMDMHDLG 274



 Score = 31.2 bits (69), Expect = 6e-05
 Identities = 17/64 (26%), Positives = 33/64 (51%), Gaps = 8/64 (12%)

Query: 444 PTLVMGVASDILFPAWQQREVAEAIRLAGNRNVTHVELSEEMSMFGHDTFLLDLKYIGNN 503
           P  ++ + SDIL+P  +Q E+A   +L  + ++ ++        +GHD FL+    +   
Sbjct: 290 PVAILSITSDILYPPEEQEELA---KLIPDSSIGYLR-----EPYGHDAFLILTDEVSAM 341

Query: 504 LRMF 507
           +R F
Sbjct: 342 VRQF 345


Lambda     K      H
   0.317    0.134    0.413 

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: 505
Number of extensions: 25
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 509
Length of database: 357
Length adjustment: 32
Effective length of query: 477
Effective length of database: 325
Effective search space:   155025
Effective search space used:   155025
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: 51 (24.3 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