GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Methylotuvimicrobium alcaliphilum 20Z

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 WP_014148952.1 MEALZ_RS12220 prephenate dehydratase

Query= BRENDA::O30012
         (620 letters)



>NCBI__GCF_000968535.2:WP_014148952.1
          Length = 361

 Score =  164 bits (416), Expect = 5e-45
 Identities = 110/337 (32%), Positives = 174/337 (51%), Gaps = 14/337 (4%)

Query: 266 IEELRGLIKSIDSLILRLIERRIDAARQIARIKMERGEPIELKDVEEEKLW----EVMSK 321
           + +LR  I +ID  IL+LI +R   A ++A+ KM  GE       + E L     + +++
Sbjct: 7   LADLRARIDAIDEQILQLINQRASCAIEVAKTKMAEGESGCFYRPDRESLVLRRVKALNQ 66

Query: 322 TTLNPVKLKEIFEGIMSLAKEEEYKVAGVKYTIAVLGPQGSFSEEMALKLVGSRVPLRYC 381
             L        F  +MS     E  +      +A LGP+G+F+++ A+K  G  V     
Sbjct: 67  GPLADETAMRFFRELMSACLALEKPL-----DVAFLGPEGTFTQQAAIKHFGHAVNAVPA 121

Query: 382 STTDEIIKLVESGEVDYGLVPIENSVNGTVLPVIDALLNHDVEVFGEAKLEVNHCLVAKR 441
            T  EI   VE+    +G+VP+ENS  G V   +D  ++  +++ GE +L V+H L+   
Sbjct: 122 MTIAEIFNAVENEHCQFGVVPVENSTEGVVNHTLDRFVSSPLKICGEVELRVHHNLIGNA 181

Query: 442 KIELKEIKTIYSHPQAVAQCMGFINNYLPSVAIRYTTSTSDAARML--DDYSAAIMSENA 499
              L +I  ++SH Q++AQC  +++ +LP        S  +AAR+       AAI  + A
Sbjct: 182 G-SLADIAEVFSHQQSLAQCRQWLDLHLPDAKRTAVNSNGEAARLAAGSKDKAAIAGKFA 240

Query: 500 ARFYRLHVLRKGIQDLKGRNITRFYLIRRRSGRSEGKI-TSLFFGVEDKPGALKDVLEVF 558
           A  Y L V+ + I+D +  N TRF +I R+     GK  TSL     ++PGAL  VLE F
Sbjct: 241 AELYGLSVIERNIED-ESNNTTRFIIIGRQISGPTGKDKTSLLVSTGNQPGALYRVLEPF 299

Query: 559 HKKGFNLRKLESRPAGTGLGDYVFFVEVEAPLREEDL 595
              G  +  +ESRP+  GL DYVFF+++E    +E++
Sbjct: 300 AHHGIGMMHIESRPSRQGLWDYVFFIDIEGHAEDENV 336


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: 397
Number of extensions: 14
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: 361
Length adjustment: 33
Effective length of query: 587
Effective length of database: 328
Effective search space:   192536
Effective search space used:   192536
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 Jul 25 2024. The underlying query database was built on Jul 25 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