GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Dyella japonica UNC79MFTsu3.2

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate N515DRAFT_4362 N515DRAFT_4362 homoserine O-acetyltransferase

Query= SwissProt::Q8P6V8
         (369 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4362
          Length = 339

 Score =  253 bits (645), Expect = 7e-72
 Identities = 149/333 (44%), Positives = 190/333 (57%), Gaps = 15/333 (4%)

Query: 44  PAADSDAPPAVRGELVINLPMRHAGQR------------ELRLRYELVGAEQAPVVFVAG 91
           P   + AP  V G + ++L  + + +R            E+ +RY   GA  AP V V G
Sbjct: 7   PVTSASAPCTVAGAVRVDLTTQRSSRRIRLSPKYGSRPCEVDVRYLWCGAPDAPTVIVQG 66

Query: 92  GISAHRHLAASAVFPEKGWVEGLVGAGRALDPASRRLLAFDFLGADGSLDAP--IDTADQ 149
           GISA+R + A       GW +  VGAGR +D    R+L  D+L     LD    + + DQ
Sbjct: 67  GISANREVVALDDEATPGWWQEAVGAGRPIDLDRYRVLCIDWL-TPAELDGATAVSSEDQ 125

Query: 150 ADAIAALLDALGIARLHGFVGYSYGALVGLQFASRHAARLHTLVAVSGAHRAHPYAAAWR 209
           ADA+AAL++ALGIAR+H F+G SYGA+ GL FA+RH   L  LV ++GAHR HP A A R
Sbjct: 126 ADALAALVEALGIARVHAFIGSSYGAMAGLAFAARHPYALDRLVLLAGAHRPHPLATAQR 185

Query: 210 ALQRRAVALGQLQCAEHHGLALARQFAMLSYRTPEEFSERFDAPPELINGRVRVAAEDYL 269
           A+QR  V LG         L+LARQ AM +YR  EEFS RF A PE   GR     EDYL
Sbjct: 186 AVQRGIVRLGVETGQPEQALSLARQLAMTTYRGSEEFSRRFTAAPEFREGRFHFPVEDYL 245

Query: 270 DAAGAQYVARTPVNAYLRLSESIDLHRIDPAAVAVPTVVVAVEGDRLVPLADLVSLVEGL 329
              G ++V R  V  +L LSESIDLH + P  +A P  ++    DRLVPL+DL  L   L
Sbjct: 246 VHQGRRFVERFDVERFLALSESIDLHDVTPERIAAPATLIGFPSDRLVPLSDLCELQRRL 305

Query: 330 GPRGSLRVLRSPFGHDAFLKEIDRIDAILTTAL 362
               +L VL SP+GHDAFLKE  R+  +L  AL
Sbjct: 306 HGPATLEVLESPYGHDAFLKETHRLAPLLRDAL 338


Lambda     K      H
   0.321    0.135    0.393 

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: 332
Number of extensions: 15
Number of successful extensions: 2
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: 369
Length of database: 339
Length adjustment: 29
Effective length of query: 340
Effective length of database: 310
Effective search space:   105400
Effective search space used:   105400
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: 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