GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Cupriavidus basilensis 4G11

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 RR42_RS04460 RR42_RS04460 chorismate mutase

Query= BRENDA::O30012
         (620 letters)



>FitnessBrowser__Cup4G11:RR42_RS04460
          Length = 379

 Score =  165 bits (418), Expect = 3e-45
 Identities = 115/364 (31%), Positives = 191/364 (52%), Gaps = 18/364 (4%)

Query: 259 ATKKAESIE--ELRGLIKSIDSLILRLIERRIDAARQIARIKMERGEPIELKDVEEEKLW 316
           A +KA  +E   LR  I ++D  +L ++ RR   A  +  +K + G P+   + E + + 
Sbjct: 19  AAEKALGVELTPLREQIDTLDRELLAMLNRRAQLALDVGEVKKKYGAPVFRPERELQVIR 78

Query: 317 EVMSKTTLNPVKLKEIFEGIMSLAKEEEYKVAGVK--YTIAVLGPQGSFSEEMALKLVGS 374
           +V      NP  L +  + + ++ +E      G++    +A LGP G+FSE+      G 
Sbjct: 79  KVQGA---NPGPLLD--DSVAAIWREVMSACRGLEKPLEVAFLGPAGTFSEQALYAHFGH 133

Query: 375 RVPLRYCSTTDEIIKLVESGEVDYGLVPIENSVNGTVLPVIDALLNHDVEVFGEAKLEVN 434
            V    C + DE+ + VE+G V+YG+VP+ENS  G V   +D  L   +++ GE  L+V+
Sbjct: 134 EVSGVPCPSIDEVFRAVEAGTVEYGVVPVENSTEGAVSRTLDLFLQTSLKISGEIALKVH 193

Query: 435 HCLVAKRKIELKEIKTIYSHPQAVAQCMGFINNYLPSVAIRYTTSTSDAARML--DDYSA 492
           H L+A    ++K +  + +H QA+AQC  ++    P +  +  +S ++AARM   D   A
Sbjct: 194 HNLMASSP-DMKGVTVVRAHAQALAQCQHWLTANYPHLERQAVSSNAEAARMASEDPTVA 252

Query: 493 AIMSENAARFYRLHVLRKGIQDLKGRNITRFYLIRRRSGRSEGK-ITSLFFGVEDKPGAL 551
           AI  E+AA  Y LH++R  IQD    N TRF +I R      G   TS+   V +K GA+
Sbjct: 253 AIAGESAANRYHLHLVRTHIQD-DPHNRTRFAVIGRYETEPSGSDQTSMILSVPNKAGAV 311

Query: 552 KDVLEVFHKKGFNLRKLESRPAGTGLGDYVFFVEVEAPLREED----LLDLKQVTTFYKV 607
             +L      G ++ + ESRPA +G  +Y F+V+VE    +      L +L++   ++KV
Sbjct: 312 YQLLAPLADNGVSMCRFESRPARSGAWEYYFYVDVEGHQHDASVARALEELRRNAAYFKV 371

Query: 608 VGVF 611
           +G +
Sbjct: 372 LGSY 375


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: 391
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: 620
Length of database: 379
Length adjustment: 34
Effective length of query: 586
Effective length of database: 345
Effective search space:   202170
Effective search space used:   202170
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: 52 (24.6 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