GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Pseudomonas fluorescens FW300-N2C3

Align cystathionine beta-synthase (O-acetyl-L-serine) (EC 2.5.1.134) (characterized)
to candidate AO356_15115 AO356_15115 cystathionine gamma-synthase

Query= BRENDA::O05394
         (379 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_15115
          Length = 417

 Score =  280 bits (715), Expect = 7e-80
 Identities = 152/342 (44%), Positives = 215/342 (62%), Gaps = 5/342 (1%)

Query: 37  GQHTGYEYSRTANPTRTALEALVTELESGEAGYAFSSGMAAITAVMMLFNS-GDHVVLTD 95
           G+  G+ YSR +NPT   LEA + ELE  E+  AFSSGMAAI++V+  F + GD VV T 
Sbjct: 57  GKAPGFIYSRMSNPTVETLEAKIRELEMAESAVAFSSGMAAISSVLYTFLAHGDRVVSTK 116

Query: 96  DVYGGTYRVMTKVLNRLGIESTFVDTSSREEVEKAIRPNTKAIYIETPTNPLLKITDLTL 155
           D YGGT ++  + L R G+  T  +T   +++E+ I    + +Y+ETPTNP LKI D+  
Sbjct: 117 DSYGGTNKIFEEFLPRTGVAVTLCETFDHDDIEREIAKGCQVLYLETPTNPTLKILDIPR 176

Query: 156 MADIAKKAGVLLIVDNTFNTPYFQQPLTLGADIVLHSATKYLGGHSDVVGGLVVTASKEL 215
           +   AK+ G +++ DNTF TP  Q PL LG D+V+HSATK+L GH DV+GGLV      +
Sbjct: 177 LVAAAKRVGAVVVADNTFATPLNQSPLALGVDVVIHSATKFLSGHGDVLGGLVCGREALM 236

Query: 216 GEELHFVQNSTGGVLGPQDSWLLMRGIKTLGLRMEAIDQNARKIASFLENHPAVQTLYYP 275
            +  H+ +   G  L P  ++L++RG+KTL LRM     +AR +A FL   P V+++ YP
Sbjct: 237 AKVRHY-REINGASLDPFSAYLIIRGMKTLALRMRQQQHSARALAEFLCTEPLVESVNYP 295

Query: 276 GSSNHPGHELAKTQGAGFGGMISFDI-GSEERVDAFLGNLKLFTIAESLGAVESLISVPA 334
           G  +HP H +A  Q +GFG ++SF + G  + V   L  L+    A +LGAVE++   PA
Sbjct: 296 GLPSHPNHAVACAQMSGFGAIVSFVLAGGMDTVKLLLPRLRFAHCAGNLGAVETIYG-PA 354

Query: 335 RMT-HASIPRERRLELGITDGLIRISVGIEDAEDLLEDIGQA 375
           R T H     E R  LGI++GL+R+SVGIED +DLL+D+ QA
Sbjct: 355 RTTSHVENTLEERQALGISEGLVRVSVGIEDTDDLLDDLKQA 396


Lambda     K      H
   0.316    0.134    0.375 

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: 409
Number of extensions: 17
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: 379
Length of database: 417
Length adjustment: 31
Effective length of query: 348
Effective length of database: 386
Effective search space:   134328
Effective search space used:   134328
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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