GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Pseudomonas stutzeri RCH2

Align Homoserine O-acetyltransferase; HAT; EC 2.3.1.31; Homoserine transacetylase; HTA (uncharacterized)
to candidate GFF2318 Psest_2366 Homoserine acetyltransferase

Query= curated2:Q67NS3
         (383 letters)



>FitnessBrowser__psRCH2:GFF2318
          Length = 340

 Score =  119 bits (298), Expect = 1e-31
 Identities = 111/340 (32%), Positives = 151/340 (44%), Gaps = 48/340 (14%)

Query: 27  LESGQRLTDVTLCYEVFGRLNPAGDNAILVCHALTGDSHVAGRYRPDDPKPGWWDDAVGP 86
           LE+G+RL +  LCY+V G  N A DN +L+       S+  G +    P  G    A GP
Sbjct: 18  LENGERLRNARLCYQVVGTPNRARDNLVLI------PSYYGGTHWGSLPLLG----ADGP 67

Query: 87  GKALDTDRYCVICSNVLGGCQGSTGPSSVNPATGRPYGLDFPLVTVRDMVRAQARLLDLL 146
              L    YCV+ +N+ G    ST PS+  P  G     DFP V++ D VRAQ  LLD L
Sbjct: 68  ---LAGGEYCVVLTNLFGA-GWSTSPSNAAPGQG---AADFPRVSLLDNVRAQKALLDRL 120

Query: 147 GVR--RLLAVIGGSLGAMQALEWAATYPDRMRGIIPIGGAGRFHPQGIAFNEVQRQAILN 204
                +L  V G S+G MQ L WA  YP+R+R I+P        P    F E  + A+  
Sbjct: 121 YGEDWQLALVTGWSMGGMQTLFWAMAYPERVRAILPFCCTAHCWPHNRVFLEGVKAALCA 180

Query: 205 DPGFLGGQYYGTPGPVRGL-ATARMLGMITYRS---DESMWTQFGRNPQGEANPLHQGFA 260
           D  +LGG+Y  +  P RGL A  R      Y      + +W + G               
Sbjct: 181 DAAWLGGRY--SVPPERGLRAFGRAYAGWAYSQAFYRQELWRELGFE------------- 225

Query: 261 VAYQVESYLHYQGRKLVERFDANSYLYLTRAMDLMDLGR--GRGSYEEAHARIQARVLAV 318
               +E+ L Y  +  +E+ DAN  L +       D  R    GS  EA  R++AR + +
Sbjct: 226 ---SLEALLDYWEQDHLEQ-DANDLLCVLHTWQSADPARSFAAGSLAEALGRVRARSILM 281

Query: 319 GIRSDLLFPTYLQRETVELVRASGGRAEYVEMDSPWGHDA 358
              SDL F     R    L+      AE   ++S WGH A
Sbjct: 282 PGSSDLYFTVEDARHEAALIPG----AELRVLESDWGHCA 317


Lambda     K      H
   0.321    0.140    0.432 

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: 382
Number of extensions: 14
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: 383
Length of database: 340
Length adjustment: 29
Effective length of query: 354
Effective length of database: 311
Effective search space:   110094
Effective search space used:   110094
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