GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Oleispira antarctica

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_046007572.1 OLEAN_RS00375 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>NCBI__GCF_000967895.1:WP_046007572.1
          Length = 397

 Score =  217 bits (552), Expect = 5e-61
 Identities = 131/362 (36%), Positives = 192/362 (53%), Gaps = 16/362 (4%)

Query: 6   PPASRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAAS--RP 63
           P   RF E      +R G  L    + YET+G LNA   NA+L+   LS D HAA     
Sbjct: 15  PKVQRFDE---PLTLRSGRILESYELIYETYGELNADASNAILICHALSGDHHAAGYHSM 71

Query: 64  DDPTPGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSI 123
           +D  PGWW++ +GPGK +DT+ + V+ +N+LG C GSTGP S +P TG+ Y   FP +++
Sbjct: 72  EDKRPGWWDSCIGPGKSIDTNKFFVVSLNNLGGCSGSTGPTSINPETGKAYGPDFPIVAV 131

Query: 124 EDIADAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSI 183
            D   +       L I + A V+G S+GGM  L    ++PE  R  + ++ A      +I
Sbjct: 132 RDWVRSQKRLADFLKIQQWAAVIGGSLGGMQVLRWSIQYPERLRHALVIASAPKLSAQNI 191

Query: 184 AVRSLQREAIRSDPGWLQGHY-DEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGE 242
           A   + R+AI  DP +  G Y D G  P+ G+  AR LG +TY S      +FGR     
Sbjct: 192 AFNEVARQAISKDPDFHNGRYMDHGVVPKAGLSQARMLGHLTYMSGDAMKEKFGRD---- 247

Query: 243 RRRADQ--GRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAP 300
             +AD+    F PEF+VESYL +  Q+F+ +FD N+Y+ ++ A+D FD        G   
Sbjct: 248 -LKADELSFSFSPEFQVESYLHYQGQKFSTQFDANTYMLMTKALDYFD--PTVDHDGDLV 304

Query: 301 GALSRMRVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIE 360
             LS+ +  +  V+   TD  F   + +EI + L     DVS+  + +  GHDAFL+ I 
Sbjct: 305 KCLSQAQC-KFFVVSFTTDWRFAPDRSEEIVNALIQADKDVSYACIASENGHDAFLLPIP 363

Query: 361 RF 362
           R+
Sbjct: 364 RY 365


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: 427
Number of extensions: 25
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: 374
Length of database: 397
Length adjustment: 30
Effective length of query: 344
Effective length of database: 367
Effective search space:   126248
Effective search space used:   126248
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