GapMind for Amino acid biosynthesis

 

Alignments for a candidate for preph-dehydratase in Desulfurobacterium atlanticum DSM 15668

Align Bifunctional chorismate mutase/prephenate dehydratase; Chorismate mutase-prephenate dehydratase; P-protein; EC 5.4.99.5; EC 4.2.1.51 (characterized)
to candidate WP_089323438.1 CHB58_RS07210 prephenate dehydratase

Query= SwissProt::P27603
         (365 letters)



>NCBI__GCF_900188395.1:WP_089323438.1
          Length = 360

 Score =  306 bits (784), Expect = 6e-88
 Identities = 164/359 (45%), Positives = 234/359 (65%), Gaps = 9/359 (2%)

Query: 7   LKALRVRIDSLDERILDLISERARCAQEVARVKTASWPKAEEAVFYRPEREAWVLKHIME 66
           L+ LR  ID +D +I+DL+S RA+ A EV  VK     + +   FY PEREA +L  + E
Sbjct: 4   LEELRKEIDGIDRQIIDLLSRRAKLASEVGEVK-----RKKGLPFYVPEREAEILTKLEE 58

Query: 67  LNK--GPLDNEEMARLFREIMSSCLALEQPLRVAYLGPEGTFSQAAALKHFGHSVISKPM 124
           LNK  G L  E +  +FREI+S+C ALE+P +V++LGP  TF+  AALKHFG S   +PM
Sbjct: 59  LNKNYGVLPPESIRAIFREIISACRALEEPTKVSFLGPYATFTHLAALKHFGTSSDLRPM 118

Query: 125 AAIDEVFREVVAGAVNFGVVPVENSTEGAVNHTLDSFLEHDIVICGEVELRIHHHLLVGE 184
            +I +VF EV  G V++GVVPVENS EG VN+T+D FL+ ++ ICGE+ + ++ HLL  E
Sbjct: 119 TSITDVFEEVDKGRVDYGVVPVENSIEGIVNYTVDMFLDTELKICGEIFVPVNLHLLSRE 178

Query: 185 TTKTDRITRIYSHAQSLAQCRKWLDAHYPNVERVAVSSNADAAKRVKSEWNSAAIAGDMA 244
           T+  + I ++YSH  ++AQ +KWL  + P+ E + VSS A AA+    E   AAIA + A
Sbjct: 179 TS-LENIEKVYSHRHAIAQAKKWLAENLPDAEVIEVSSTAKAAELASKEKGVAAIASEAA 237

Query: 245 AQLYGLSKLAEKIEDRPVNSTRFLIIGSQE-VPPTGDDKTSIIVSMRNKPGALHELLMPF 303
           A LY L+ L   I++   N TRF ++G ++   PTG+DKTSI+ S ++  GAL   L PF
Sbjct: 238 ALLYDLNILERNIQEISKNFTRFFVVGKKDSETPTGNDKTSIMFSTKHVAGALFHALKPF 297

Query: 304 HSNGIDLTRIETRPSRSGKWTYVFFIDCMGHHQDPLIKNVLEKIGHEAVALKVLGSYPK 362
               ++LT+IE+RP++   W YVFF+D  GH  +P +K  LE++  +   +K+LGSYPK
Sbjct: 298 ALYDVNLTKIESRPTKKRPWEYVFFVDIDGHKTEPRVKKALEEVAKDTSFMKILGSYPK 356


Lambda     K      H
   0.319    0.133    0.390 

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: 315
Number of extensions: 15
Number of successful extensions: 5
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: 365
Length of database: 360
Length adjustment: 29
Effective length of query: 336
Effective length of database: 331
Effective search space:   111216
Effective search space used:   111216
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: 49 (23.5 bits)

This GapMind analysis is from Apr 10 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