GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Steroidobacter denitrificans DSM 18526

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_066919752.1 ACG33_RS06625 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>NCBI__GCF_001579945.1:WP_066919752.1
          Length = 365

 Score =  389 bits (998), Expect = e-113
 Identities = 199/363 (54%), Positives = 252/363 (69%), Gaps = 4/363 (1%)

Query: 8   ASRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASRPDDPT 67
           A + ++L   F M RGG L G  IAYET+G      DNA+L+ TGL+P AHAAS   DP+
Sbjct: 4   ARKILKLDRPFEMHRGGTLQGVEIAYETWGDPAHRGDNAILIFTGLTPSAHAASSESDPS 63

Query: 68  PGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIA 127
           PGWWE M+GPG+P+DT  + VICVNSLGS  GST P S +P TG  YRL+FP L++EDIA
Sbjct: 64  PGWWEDMIGPGRPIDTRRFFVICVNSLGSPFGSTSPVSINPATGRAYRLTFPVLTVEDIA 123

Query: 128 DAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRS 187
            A    V +LGI +L  VVG S+GGM+ LA  A  P  AR+ +S+S A  +LPF+IA+RS
Sbjct: 124 HAGHEVVVSLGIEKLLAVVGPSLGGMTVLAYCALFPGAARSVVSISAAARSLPFAIALRS 183

Query: 188 LQREAIRSDPGWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRAD 247
           LQRE IR D  W +G Y     P  GM  ARKLGM+TYRSA+EW  RFGR R   +RR  
Sbjct: 184 LQREIIRRDSAWREGDYAADAIPVEGMRLARKLGMITYRSAKEWGLRFGRERADLQRRPG 243

Query: 248 QGRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRMR 307
              FG +FEVESYL+ HA++F  ++DPN YLY+S AMD FDL D    GG    AL R  
Sbjct: 244 D-PFGIDFEVESYLENHAEKFTGQYDPNCYLYISRAMDLFDLAD---HGGSVNEALRRFT 299

Query: 308 VERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPVA 367
           VERALV+G  TD+LFP+ QQQE+A+GL+AGG +V+F+ + +  GHD+FLVD++RF P +A
Sbjct: 300 VERALVIGVETDLLFPIEQQQELAEGLAAGGREVTFVRLPSLQGHDSFLVDMDRFRPVIA 359

Query: 368 KFL 370
           +FL
Sbjct: 360 EFL 362


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: 469
Number of extensions: 19
Number of successful extensions: 3
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: 365
Length adjustment: 30
Effective length of query: 344
Effective length of database: 335
Effective search space:   115240
Effective search space used:   115240
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: 49 (23.5 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