GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Halomonas desiderata SP1

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_086510438.1 BZY95_RS13465 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>NCBI__GCF_002151265.1:WP_086510438.1
          Length = 385

 Score =  231 bits (590), Expect = 2e-65
 Identities = 139/364 (38%), Positives = 199/364 (54%), Gaps = 13/364 (3%)

Query: 16  DGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASR--PDDPTPGWWEA 73
           D  A+  G  L    + YET+G+LNA R NAVL+   LS   HAA     D+  PGWW+A
Sbjct: 21  DPLALACGRTLPAYDLVYETYGTLNAERSNAVLICHALSGHHHAAGYHDADERKPGWWDA 80

Query: 74  MVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIADAAAHT 133
            +GPGK +DT+ + V+ +N+LG C GSTGP ST+P TG  +   FP +++ D   + A  
Sbjct: 81  HIGPGKSIDTNRFFVVSLNNLGGCHGSTGPISTNPATGRQWGPDFPMVTVSDWVHSQARL 140

Query: 134 VRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRSLQREAI 193
              LGI R A  +G S+GGM  L     +PE     + ++        +IA   + R+AI
Sbjct: 141 ADRLGIERFAAAIGGSLGGMQVLQWTRLYPERVANAVIIAATPKLSAQNIAFNEVARQAI 200

Query: 194 RSDPGWLQGHYDE-GEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRADQGRFG 252
           RSDP +  G Y E G  PRRG+  AR +G +TY S      +FGR       R++   FG
Sbjct: 201 RSDPDFHDGWYAEHGTAPRRGLKLARMVGHITYLSEDAMGSKFGRD-----LRSEDLNFG 255

Query: 253 --PEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRMRVER 310
              EF+VESYL +    F+  FD N+YL ++ A+D FD       GG    A++  +   
Sbjct: 256 YDVEFQVESYLRYQGDTFSTAFDANTYLLMTKALDYFD--PAAEHGGVLAEAVAPCQ-GP 312

Query: 311 ALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPVAKFL 370
            LV+   +D  FP S+ +E+A+ L   G  VS++ +D+P GHDAFL+   R+    A F+
Sbjct: 313 FLVVSFTSDWRFPPSRSRELANALIRAGKRVSYVNIDSPHGHDAFLLPEPRYQAVFAAFM 372

Query: 371 AIVA 374
           + VA
Sbjct: 373 SRVA 376


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: 448
Number of extensions: 22
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: 385
Length adjustment: 30
Effective length of query: 344
Effective length of database: 355
Effective search space:   122120
Effective search space used:   122120
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 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