GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Pseudomonas putida KT2440

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate PP_5097 PP_5097 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>FitnessBrowser__Putida:PP_5097
          Length = 379

 Score =  242 bits (617), Expect = 1e-68
 Identities = 138/373 (36%), Positives = 208/373 (55%), Gaps = 11/373 (2%)

Query: 5   IPPASRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAAS--R 62
           +P  +RF E     A+  G +L    + YET+G+LNA+  NAVL+   LS   HAA    
Sbjct: 14  VPQTARFDE---PLALACGRSLASYELVYETYGTLNASASNAVLICHALSGHHHAAGYHA 70

Query: 63  PDDPTPGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELS 122
             D  PGWW++ +GPGKP+DT+ + V+ +N+LG C GSTGP+S +P TG+PY   FP L+
Sbjct: 71  ATDRKPGWWDSCIGPGKPIDTNRFFVVSLNNLGGCNGSTGPSSVNPATGKPYGADFPVLT 130

Query: 123 IEDIADAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFS 182
           +ED   +       LGI + A VVG S+GGM AL     +PE  R  + ++ A      +
Sbjct: 131 VEDWVHSQVRLGERLGIQQWAAVVGGSLGGMQALQWTISYPERVRHCVDIASAPKLSAQN 190

Query: 183 IAVRSLQREAIRSDPGWLQGHY-DEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIG 241
           IA   + R+AI +DP +  G + D+G  P+RG++ AR +G +TY S      +FGR    
Sbjct: 191 IAFNEVARQAILTDPEFHGGSFQDQGVIPKRGLMLARMVGHITYLSDDSMGEKFGRELKS 250

Query: 242 ERRRADQGRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPG 301
           ++   D      EF+VESYL +  + F+ RFD N+YL ++ A+D FD       GG    
Sbjct: 251 DKLNYD--FHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFD--PAATHGGDLAA 306

Query: 302 ALSRMRVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIER 361
            L+ +  +   +M   TD  F  ++ +EI D L A   +V +L +D+P GHDAFL+   R
Sbjct: 307 TLAHVTADYC-IMSFTTDWRFSPARSREIVDALMAARKNVCYLEIDSPYGHDAFLIPTPR 365

Query: 362 FGPPVAKFLAIVA 374
           +    + ++  +A
Sbjct: 366 YMQGFSNYMNRIA 378


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: 418
Number of extensions: 21
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: 379
Length adjustment: 30
Effective length of query: 344
Effective length of database: 349
Effective search space:   120056
Effective search space used:   120056
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