GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Desulfovibrio vulgaris Hildenborough

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 209398 DVU0462 chorismate mutase/prephenate dehydratase

Query= BRENDA::O30012
         (620 letters)



>MicrobesOnline__882:209398
          Length = 391

 Score =  162 bits (410), Expect = 2e-44
 Identities = 111/338 (32%), Positives = 182/338 (53%), Gaps = 16/338 (4%)

Query: 263 AESIEELRGLIKSIDSLILRLIERRIDAARQIARIKMERGEP-IELKDVEEEKLWEVMSK 321
           A+ ++ +R  I  +D  +L L+ RR   + ++ RIK    +P I  +   E ++++ +  
Sbjct: 15  AQRLQAIRVTIDGLDRDLLALLNRRAALSLEVGRIKAT--DPGIVFRPFREREVFDNLEA 72

Query: 322 TTLNPVK---LKEIFEGIMSLAKEEEYKVAGVKYTIAVLGPQGSFSEEMALKLVGSRVPL 378
               P+    L+ I+  I+S ++  +         +A LGP+G+FS    ++ +G  +  
Sbjct: 73  ANEGPLPDEHLRAIWREIISSSRSLQRP-----QRVAYLGPEGTFSYFAGMEFLGRAMDY 127

Query: 379 RYCSTTDEIIKLVESGEVDYGLVPIENSVNGTVLPVIDALLNHDVEVFGEAKLEVNHCLV 438
           R      ++ + V   + + G+VP+ENS+ GTV   +D  L H+V +  E    ++HCL+
Sbjct: 128 RPQPGLPDVFRAVHDRQCELGIVPLENSLQGTVGQSLDLFLQHEVFIQAELFCRISHCLL 187

Query: 439 AKRKIELKEIKTIYSHPQAVAQCMGFINNYLPSVAIRYTTSTSDAARML--DDYSAAIMS 496
                 L +I T+YSHPQ +AQC G++  +LP+  I  T ST+ AAR    +  +AAI  
Sbjct: 188 G-TAAALADIDTVYSHPQPLAQCGGWLRAHLPNARIIPTESTAAAARRAAGEAGAAAIGH 246

Query: 497 ENAARFYRLHVLRKGIQDLKGRNITRFYLIRRRSGRSEGK-ITSLFFGVEDKPGALKDVL 555
            + A    L+VL +GI+D +  N TRF +I       +G+  TS+ F + DK GAL  VL
Sbjct: 247 RSLADLLGLNVLERGIED-QPDNWTRFVVIAPAPADQQGREKTSMLFSLPDKAGALAGVL 305

Query: 556 EVFHKKGFNLRKLESRPAGTGLGDYVFFVEVEAPLREE 593
           E+  ++G N++KLESRP       YVFFV+VE  L  E
Sbjct: 306 ELLAREGINMKKLESRPLRGEKWQYVFFVDVECDLGTE 343


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: 415
Number of extensions: 15
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: 391
Length adjustment: 34
Effective length of query: 586
Effective length of database: 357
Effective search space:   209202
Effective search space used:   209202
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.

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