GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Paraburkholderia bryophila 376MFSha3.1

Align Alanine--glyoxylate aminotransferase; AGT; Serine--pyruvate aminotransferase; SPT; EC 2.6.1.44; EC 2.6.1.51 (characterized)
to candidate H281DRAFT_04750 H281DRAFT_04750 aspartate aminotransferase

Query= SwissProt::P31030
         (392 letters)



>FitnessBrowser__Burk376:H281DRAFT_04750
          Length = 407

 Score =  186 bits (471), Expect = 1e-51
 Identities = 120/358 (33%), Positives = 185/358 (51%), Gaps = 10/358 (2%)

Query: 24  LLLGPGPSNLPPRVLAAGGLQMIGHMHEEMYQVMDEIKQGIQYAFQTRNALTLAVSGSGH 83
           L++G GP  +P  V  A  + +I H+   M +V+ ++K   +Y FQT +   L V+G G 
Sbjct: 31  LMMGAGPVPIPAAVAKANTI-VINHLGATMVKVIGQVKTMARYVFQTNSKWVLGVAGPGS 89

Query: 84  CALETALFNLLEPGDAFLVGANGIWGQRAAEVGERIGARVHPMIKDPGSHYTLQEVEECL 143
            A+E A+ NL   G   L   NG +  R AE+G R+GARV  +     +  +L E+ E +
Sbjct: 90  AAMEMAISNLAWEGTRVLSIKNGFFSGRMAEMGRRVGARVTELEVADRTVASLDEIAEAI 149

Query: 144 AQHKPVLLFLTHGESSTGVLQ-PLDGFGELCHRYKCLLLVDSVASLGGAPIYMDQQGIDV 202
            + +P ++ +  GE+S  V    L     L      L++VD+V +L   P+ MD  GID 
Sbjct: 150 RRERPEIVTVVQGETSNTVWNYQLKDIAALAKAAGALVIVDAVCTLSTMPLAMDAWGIDA 209

Query: 203 LYSGSQKALNAPPGTSLISFSDKAKSKIYARKTKPFSFYMDVQLLANIWGCDGKPRMYHH 262
           + +G QK L++ PG SLI+FSD A  ++  R      + +D  L  N W   G    YH+
Sbjct: 210 VITGGQKGLSSIPGVSLIAFSDAAWERVKGRTAPNAHWCLDASLAENFWHNAG----YHY 265

Query: 263 TTPVIGIFALRESLALLVEQGLEKSWQRHREVAQHLYRRLQELGLQLFVKDPALRLPTVT 322
           T PV G+ AL E+L L+  + LEK + RH + +  L   +  LGLQL+    A RL +V 
Sbjct: 266 TAPVSGVLALHEALRLVCAETLEKRFARHLKCSVALQEGVTALGLQLYA-PVACRLNSVV 324

Query: 323 TVIVPASYRWRDIVSYVMHHFGIEITGGLGPSADKVLRIGLLGCNATRENVDRLATAL 380
            + VPA     D+ +++     +EI+G  G     ++RIG +G      N+ R   AL
Sbjct: 325 GIEVPAGLSPGDVCAHISRQHQVEISGSFGL---PIVRIGQMGEQCREHNLFRTLHAL 379


Lambda     K      H
   0.322    0.138    0.420 

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: 327
Number of extensions: 23
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: 392
Length of database: 407
Length adjustment: 31
Effective length of query: 361
Effective length of database: 376
Effective search space:   135736
Effective search space used:   135736
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.

Links

Downloads

Related tools

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