GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Methanobacterium lacus AL-21

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_013644807.1 METBO_RS06075 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>NCBI__GCF_000191585.1:WP_013644807.1
          Length = 489

 Score =  257 bits (656), Expect = 5e-73
 Identities = 138/365 (37%), Positives = 212/365 (58%), Gaps = 10/365 (2%)

Query: 9   SRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASRPD-DPT 67
           +++  L D   +  G  L   ++AYET+G LN  + NA+LV   L+ DAH A   + D  
Sbjct: 11  TKYHSLSDDLILESGEKLKNVQVAYETYGKLNKEKSNAILVCHALTGDAHVAGWYEGDKK 70

Query: 68  PGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIA 127
           PGWW+ ++GPGK +DT+ + +IC N +G CKGSTGP+S +P T +PY L FP ++I+D+ 
Sbjct: 71  PGWWDVIIGPGKCLDTEKYFIICSNVIGGCKGSTGPSSINPETNKPYGLDFPIITIKDMV 130

Query: 128 DAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRS 187
           +A    V ++G+++L  V+G SMGGM  L     +P++ R+ I ++    + P  IA   
Sbjct: 131 NAQKKLVNSMGVTQLFAVIGGSMGGMQVLQWCVSYPDMVRSAIPIATTAFSSPQQIAFNE 190

Query: 188 LQREAIRSDPGWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRAD 247
           + R AI SDP W  G Y + E P  G+  AR +  +TY S +    +FGR R+ ++   D
Sbjct: 191 VGRRAIISDPNWNNGQYYDSEVPTEGLALARMIAHITYLSNESMYQKFGR-RLQDKE--D 247

Query: 248 QG-RFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRM 306
            G  F  +FEVESYL +    F  RFD NSYLY++ A+D FDL     G G        +
Sbjct: 248 YGFDFETDFEVESYLHYQGNSFTKRFDANSYLYITKAVDYFDL----AGEGSLAETFYGL 303

Query: 307 RVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPV 366
           ++ + LV+   +D L+P S  ++I  GL+A   +VS+  + +  GHDAFL++  +    +
Sbjct: 304 KI-KFLVISVDSDWLYPPSLSRDIVMGLNANDINVSYCEIKSSYGHDAFLIEAGQLNYLI 362

Query: 367 AKFLA 371
           A FL+
Sbjct: 363 AGFLS 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: 428
Number of extensions: 15
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: 489
Length adjustment: 32
Effective length of query: 342
Effective length of database: 457
Effective search space:   156294
Effective search space used:   156294
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: 51 (24.3 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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