GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Azospirillum brasilense Sp245

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate AZOBR_RS14580 AZOBR_RS14580 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>FitnessBrowser__azobra:AZOBR_RS14580
          Length = 398

 Score =  182 bits (463), Expect = 1e-50
 Identities = 117/359 (32%), Positives = 187/359 (52%), Gaps = 16/359 (4%)

Query: 23  GGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASR--PDDPTPGWWEAMVGPGKP 80
           GG +   RI +E++G LN ARDN +LV    S ++HAA +   +DP PG+W++++GPGKP
Sbjct: 45  GGTIKNVRIGWESYGKLNDARDNVILVTHFFSGNSHAAGKYKMEDPAPGYWDSIIGPGKP 104

Query: 81  VDTDLWHVICVNSLGSCKG------STGPASTDPRTGEPYRLSFPELSIEDIADAAAHTV 134
           +DTD + +I  ++L +         +TGPAS +P TG+PY +SFP ++I D  +     +
Sbjct: 105 LDTDKFFIISSDTLVNLSPKDPTVTTTGPASVNPDTGKPYGMSFPVVTIRDFVNVQKALL 164

Query: 135 RALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRSLQREAIR 194
            +L +  L  V+G SMG + AL   A HPE+ +  +++ G   A PF I   +L    IR
Sbjct: 165 DSLNVKSLHAVMGGSMGSLQALEWGATHPEMVKRVVAVIGGAEADPFLIGWLNLWAAPIR 224

Query: 195 SDPGWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRADQGRFGPE 254
            DP W  G Y     P+ G+  A KL  +  R  +  D  FGR    E  +        +
Sbjct: 225 VDPNWQGGDYYGKAEPKAGLTEALKLVTLHARHWKWADATFGR-GWAEEGKDPAASMNNQ 283

Query: 255 FEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRMRVERALVM 314
           + +E++LD  A   A   D N +LYL  A   F +    GGGG     L++++    L+ 
Sbjct: 284 YAIEAWLDKAAAARAAVSDANHFLYLVKANQTFLV----GGGGSLDEGLAKIKAPVLLIP 339

Query: 315 GARTDILFPLSQ-QQEIADGLSAGGADVSFL-PVDTPAGHDAFLVDIERFGPPVAKFLA 371
            A  D++FP  +  + + + L   G  V++   + T  GH   + +I + G  ++ F+A
Sbjct: 340 SA-DDLVFPPERAMRPLKERLEKQGIAVTYTDAITTSLGHLDGIANIAKAGDAISAFMA 397


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: 412
Number of extensions: 19
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: 398
Length adjustment: 30
Effective length of query: 344
Effective length of database: 368
Effective search space:   126592
Effective search space used:   126592
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