GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Acidovorax sp. GW101-3H11

Align prephenate dehydrogenase (EC 1.3.1.12); prephenate dehydratase (EC 4.2.1.51); chorismate mutase (EC 5.4.99.5) (characterized)
to candidate Ac3H11_2574 Chorismate mutase I (EC 5.4.99.5) / Prephenate dehydratase (EC 4.2.1.51)

Query= BRENDA::O30012
         (620 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2574
          Length = 351

 Score =  169 bits (428), Expect = 2e-46
 Identities = 121/358 (33%), Positives = 184/358 (51%), Gaps = 32/358 (8%)

Query: 273 IKSIDSLILRLIERRIDAARQIARIKMERGEPIELKDVEEEKLWEVMSKTT-LNPVKLK- 330
           I SID  +L L+ +R   A Q+  +K   G P    D    ++ +V+ K T  NP  LK 
Sbjct: 3   IDSIDQQLLTLLNQRALVAEQVGEVKKREGTPFFRPD----RVAQVIDKITHANPGPLKG 58

Query: 331 ----EIFEGIMS--LAKEEEYKVAGVKYTIAVLGPQGSFSEEMALKLVGSRVPLRYCSTT 384
                I+  IMS  LA E   +VA       VLGP+G+F E+ A++  G    L YC+  
Sbjct: 59  PHVAAIWREIMSACLALESPQRVA-------VLGPEGTFCEQAAIEFFGGAADLMYCANF 111

Query: 385 DEIIKLVESGEVDYGLVPIENSVNGTVLPVIDALLNHDVEVFGEAKLEVNHCLVAKRKIE 444
           DE+     +G   YG+V +ENS  G V   +D  L+    V GE  L V H L+ +    
Sbjct: 112 DEVFHATAAGSAQYGVVGVENSTEGVVTRSLDLFLHTPTHVVGEVSLLVRHNLL-RTTNS 170

Query: 445 LKEIKTIYSHPQAVAQCMGFINNYLPSVAIRYTTSTSDAARM--LDDYSAAIMSENAARF 502
           L  I+ + +HPQA+AQC  +++ +LP    R  +S ++ AR+   +   AA+ SE AA  
Sbjct: 171 LDGIEAVLAHPQALAQCQAWLSKHLPHAERRPVSSNAEGARLATTNPAWAALSSERAATQ 230

Query: 503 YRLHVLRKGIQDLKGRNITRFYLI----RRRSGRSEGK-ITSLFFGVEDKPGALKDVLEV 557
           + LH++   IQD    N TRF +I      ++    GK  TSL   V ++PGA+ D+L  
Sbjct: 231 FGLHIVSHAIQD-DAYNRTRFAIICLPHTLQTPPPSGKDCTSLVVSVPNQPGAVHDLLVP 289

Query: 558 FHKKGFNLRKLESRPAGTGLGDYVFFVEVEA----PLREEDLLDLKQVTTFYKVVGVF 611
               G ++ + ESRPA TG  +Y F+++++     P     L +L+ +  FYKV+G +
Sbjct: 290 LKTHGVSMTRFESRPARTGQWEYYFYIDLDGHPAQPHVARALEELRSLCAFYKVLGTY 347


Lambda     K      H
   0.320    0.137    0.380 

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: 365
Number of extensions: 19
Number of successful extensions: 6
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: 620
Length of database: 351
Length adjustment: 33
Effective length of query: 587
Effective length of database: 318
Effective search space:   186666
Effective search space used:   186666
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: 51 (24.3 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