GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Pedobacter sp. GW460-11-11-14-LB5

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate CA265_RS08175 CA265_RS08175 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>FitnessBrowser__Pedo557:CA265_RS08175
          Length = 352

 Score =  161 bits (408), Expect = 2e-44
 Identities = 106/354 (29%), Positives = 173/354 (48%), Gaps = 30/354 (8%)

Query: 18  FAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASRPDDPTPGWWEAMVGP 77
           F +  G  +   +IAY+T+G LNA +DN + V   L+ +A            WWE + G 
Sbjct: 13  FKLESGKKIRNLQIAYQTYGKLNANKDNVIWVCHALTANADVFE--------WWEGLFGQ 64

Query: 78  GKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIADAAAHTVRAL 137
               + +  +++C N LGS  GS+ P ST+P TG PY LSFP+ +I D+  A       L
Sbjct: 65  NSLFNPEEHYIVCANVLGSHYGSSNPLSTNPVTGLPYYLSFPQFTIRDLVSAHQLLASHL 124

Query: 138 GISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRSLQREAIRSDP 197
           GI  +  ++G S+GG  A+      P      I ++      P+ IA    QR AI +D 
Sbjct: 125 GIDYIKLLIGGSLGGQQAVEWSISEPNKIENLILIATNAAHSPWGIAFNESQRLAITTDR 184

Query: 198 GWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRI-GERRRADQGRFGPEFE 256
            +   + ++  G  +G+ TAR + +++YR+       +G T++     + D       F 
Sbjct: 185 TF---YANQPNGGSKGLKTARSIALLSYRTYS----AYGSTQVESVNDKTD------NFR 231

Query: 257 VESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRMRVERALVMGA 316
             SY ++  ++  +RF+  SY YL+ AMD  ++G        A     ++     LV+G 
Sbjct: 232 SSSYQNYQGEKLINRFNAYSYYYLTKAMDSHNVGRNRKSIADA----LKLITANTLVIGI 287

Query: 317 RTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPVAKFL 370
             D+LFPLS+Q+ +AD +   GA+ S L  D   GHD FL++ +     +  F+
Sbjct: 288 ENDVLFPLSEQKYLADHIP--GAEFSALHSD--YGHDGFLIETDALTNVIGNFI 337


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: 269
Number of extensions: 14
Number of successful extensions: 6
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: 352
Length adjustment: 29
Effective length of query: 345
Effective length of database: 323
Effective search space:   111435
Effective search space used:   111435
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