GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Dyella japonica UNC79MFTsu3.2

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate N515DRAFT_4362 N515DRAFT_4362 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4362
          Length = 339

 Score =  146 bits (369), Expect = 7e-40
 Identities = 112/325 (34%), Positives = 160/325 (49%), Gaps = 47/325 (14%)

Query: 47  VLVLTGLSPDAHAASRPDDPTPGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPAST 106
           V+V  G+S +    +  D+ TPGWW+  VG G+P+D D + V+C++ L        PA  
Sbjct: 62  VIVQGGISANREVVALDDEATPGWWQEAVGAGRPIDLDRYRVLCIDWLT-------PAEL 114

Query: 107 DPRTGEPYRLSFPELSIEDIADAAAHTVRALGISRLACVVGASMGGMSALALLARHPELA 166
           D  T          +S ED ADA A  V ALGI+R+   +G+S G M+ LA  ARHP   
Sbjct: 115 DGATA---------VSSEDQADALAALVEALGIARVHAFIGSSYGAMAGLAFAARHPYAL 165

Query: 167 RTHISLSGAVHALPFSIAVRSLQREAIRSDPGWLQGHYDEGEGPRRGMLTARKLGMMTYR 226
              + L+GA    P + A R++QR  +R           E   P + +  AR+L M TYR
Sbjct: 166 DRLVLLAGAHRPHPLATAQRAVQRGIVRLGV--------ETGQPEQALSLARQLAMTTYR 217

Query: 227 SAQEWDCRFGRTRIGERRRADQGRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQ 286
            ++E+  RF  T   E R   +GRF   F VE YL    +RF +RFD   +L LS ++D 
Sbjct: 218 GSEEFSRRF--TAAPEFR---EGRF--HFPVEDYLVHQGRRFVERFDVERFLALSESIDL 270

Query: 287 FDLGDGGGGGGGAPGALSRMRVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPV 346
            D+          P  ++      A ++G  +D L PLS   E+   L  G A +  L  
Sbjct: 271 HDV---------TPERIA----APATLIGFPSDRLVPLSDLCELQRRLH-GPATLEVL-- 314

Query: 347 DTPAGHDAFLVDIERFGPPVAKFLA 371
           ++P GHDAFL +  R  P +   LA
Sbjct: 315 ESPYGHDAFLKETHRLAPLLRDALA 339


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: 330
Number of extensions: 13
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: 339
Length adjustment: 29
Effective length of query: 345
Effective length of database: 310
Effective search space:   106950
Effective search space used:   106950
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 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