GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Escherichia coli BW25113

Align succinyldiaminopimelate transaminase (EC 2.6.1.17) (characterized)
to candidate 14737 b0600 putative aminotransferase (NCBI)

Query= BRENDA::P9WPZ5
         (397 letters)



>FitnessBrowser__Keio:14737
          Length = 386

 Score =  254 bits (649), Expect = 3e-72
 Identities = 148/389 (38%), Positives = 208/389 (53%), Gaps = 13/389 (3%)

Query: 4   SRLRPYATTVFAEMSALATRIGAVNLGQGFPDEDGPPKMLQAAQDAIAGGVNQYPPGPGS 63
           S+L    TT+F +MSALA +  A+NL QGFPD DGP  + +     +A G NQY P  G 
Sbjct: 10  SKLPQLGTTIFTQMSALAQQHQAINLSQGFPDFDGPRYLQERLAHHVAQGANQYAPMTGV 69

Query: 64  APLRRAIAAQRRRHFGVDYDPETEVLVTVGATEAIAAAVLGLVEPGSEVLLIEPFYDSYS 123
             LR AIA +  R +G   D ++++ VT GATEA+ AA+  LV  G EV+  +P YDSY+
Sbjct: 70  QALREAIAQKTERLYGYQPDADSDITVTAGATEALYAAITALVRNGDEVICFDPSYDSYA 129

Query: 124 PVVAMAGAHRVTVPLVPDGRGFALDADALRRAVTPRTRALIINSPHNPTGAVLSATELAA 183
           P +A++G     + L P    F +D       ++ RTR +I+N+PHNP+  V    + AA
Sbjct: 130 PAIALSGGIVKRMALQPPH--FRVDWQEFAALLSERTRLVILNTPHNPSATVWQQADFAA 187

Query: 184 IAEIAVAANLVVITDEVYEHLVFDHARHLPLAGFDGMAERTITISSAAKMFNCTGWKIGW 243
           + +      + VI+DEVYEH+ F    H  +     + ER + +SS  K ++ TGWK+G+
Sbjct: 188 LWQAIAGHEIFVISDEVYEHINFSQQGHASVLAHPQLRERAVAVSSFGKTYHMTGWKVGY 247

Query: 244 ACGPAELIAGVRAAKQYLSYVGGAPFQPAVALALDTEDAWVAALRNSLRARRDRLAAGLT 303
              PA + A +R   QYL++    P Q A+A  L  E     AL +  R +RD L   L 
Sbjct: 248 CVAPAPISAEIRKVHQYLTFSVNTPAQLALADMLRAEPEHYLALPDFYRQKRDILVNALN 307

Query: 304 EIGFAVHDSYGTYFLCADPRPLGYDDSTEFCAALPEKVGVAAIPMSAFCDPAAGQASQQA 363
           E    +    GTYFL  D   +   D  EFC  L ++ GVAAIP+S FC          A
Sbjct: 308 ESRLEILPCEGTYFLLVDYSAVSTLDDVEFCQWLTQEHGVAAIPLSVFC----------A 357

Query: 364 DVWNH-LVRFTFCKRDDTLDEAIRRLSVL 391
           D + H L+R  F K++ TL  A  RL  L
Sbjct: 358 DPFPHKLIRLCFAKKESTLLAAAERLRQL 386


Lambda     K      H
   0.321    0.135    0.405 

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: 383
Number of extensions: 21
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: 397
Length of database: 386
Length adjustment: 31
Effective length of query: 366
Effective length of database: 355
Effective search space:   129930
Effective search space used:   129930
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 (21.9 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