GapMind for Amino acid biosynthesis

 

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

Align Anthranilate synthase component 1 2; EC 4.1.3.27; Anthranilate synthase component I 2 (uncharacterized)
to candidate H281DRAFT_04702 H281DRAFT_04702 para-aminobenzoate synthetase / 4-amino-4-deoxychorismate lyase

Query= curated2:Q9HS66
         (488 letters)



>FitnessBrowser__Burk376:H281DRAFT_04702
          Length = 629

 Score =  180 bits (456), Expect = 1e-49
 Identities = 122/302 (40%), Positives = 161/302 (53%), Gaps = 20/302 (6%)

Query: 187 RDGDPAVGPPPADSPAPFESVAGRAAFESRVRRIQDAIRDGDTFQANVSHRLDAPAAVHP 246
           +DGD A  P  A +    ESV   A F + +  I  A+RDG+++Q N ++RL       P
Sbjct: 113 QDGDLAE-PSVAGTANVRESVEP-AEFNAAIGAIHAALRDGESYQVNYTYRLGFDVFGSP 170

Query: 247 VAVFEALRDTNPAPYSGIVEFPGVDLV-SASPELLLARRGRELTTEPIAGTRPRGATPAE 305
           +A++  LR   P  Y  ++  PG   V S SPEL + ++   L   P+ GT PR A P+ 
Sbjct: 171 IALYRRLRARQPVRYGALIAMPGNGWVLSCSPELFVEKQNATLRARPMKGTAPRSADPSA 230

Query: 306 DDAARAALRADDKERAEHAMLVDLERNDLGKVSEYGSVAVPDYRRVDAYSEVLHLVSEVT 365
           D  A   L  D K RAE+ M+VDL RNDL +V++ GSV VP    V+ Y+ V  + S V 
Sbjct: 231 DRGAAEFLGNDPKNRAENVMIVDLLRNDLSRVAQTGSVKVPALFSVEPYASVWQMTSTVE 290

Query: 366 GRLRDSCSLRDAIAAVFPGGTITGAPKPRTMALIDTVEATRRGPYTGSL----------- 414
             LR   S    + A+FP G+ITGAPK RTM LID +E+T RG YTG++           
Sbjct: 291 AALRPGTSFAAIVRALFPCGSITGAPKHRTMQLIDELESTPRGLYTGAIGWLDAPVLEPA 350

Query: 415 AAIGFDGDATLSITIRTLVRR--AATYHLR----VGAGIVHDSTPAAEYDETLAKARALV 468
           A     GD  +S+ IRTL  +  A T  LR    +GAGIV DS    EY E   KAR L 
Sbjct: 351 ANENSGGDFCMSVAIRTLTLKPLAPTGELRGTMGIGAGIVLDSVAEDEYAECRLKARFLT 410

Query: 469 TA 470
            A
Sbjct: 411 GA 412


Lambda     K      H
   0.317    0.135    0.397 

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: 689
Number of extensions: 41
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: 488
Length of database: 629
Length adjustment: 36
Effective length of query: 452
Effective length of database: 593
Effective search space:   268036
Effective search space used:   268036
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 (21.7 bits)
S2: 53 (25.0 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