GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Methylovulum miyakonense HT12

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_019866292.1 METMI_RS0110720 prephenate dehydratase

Query= BRENDA::O30012
         (620 letters)



>NCBI__GCF_000384075.1:WP_019866292.1
          Length = 361

 Score =  174 bits (440), Expect = 8e-48
 Identities = 116/331 (35%), Positives = 185/331 (55%), Gaps = 18/331 (5%)

Query: 266 IEELRGLIKSIDSLILRLIERRIDAARQIARIKMERGEPIELKDVEEEKLW----EVMSK 321
           + ELR  I ++D+ +LRL+  R   A ++A+ K+ +GE       + E L     + +++
Sbjct: 7   LAELREKIDALDAEVLRLLNERAKCAMEVAKTKIAQGEVGTFYRPDRESLVLRRIQELNE 66

Query: 322 TTLNPVKLKEIFEGIMS--LAKEEEYKVAGVKYTIAVLGPQGSFSEEMALKLVGSRVPLR 379
             L+   +   F  IMS  LA E+  +VA        LGP+G+F+++ A K  G  V   
Sbjct: 67  GPLSNDTVIRFFREIMSACLALEKPLEVA-------FLGPEGTFTQQAAFKHFGHAVKTV 119

Query: 380 YCSTTDEIIKLVESGEVDYGLVPIENSVNGTVLPVIDALLNHDVEVFGEAKLEVNHCLVA 439
             +T  EI   VE+G   +G+VP+ENS  G +   +D LL   +++ GE ++ V+  L+ 
Sbjct: 120 PAATISEIFNAVETGLCQFGVVPVENSTEGVISHTLDRLLASPLKICGEVEIRVHQNLLG 179

Query: 440 KRKIELKEIKTIYSHPQAVAQCMGFINNYLPSVAIRYTTSTSDAARML--DDYSAAIMSE 497
             +  L +I T+YSH Q++AQC  +++ YLP+      +S ++AAR+   D   AAI   
Sbjct: 180 LAE-NLADITTVYSHQQSLAQCRQWLDKYLPNPQRVAVSSNAEAARLAASDKQFAAIAGI 238

Query: 498 NAARFYRLHVLRKGIQDLKGRNITRFYLIRRRSGRSEGK-ITSLFFGVEDKPGALKDVLE 556
            AA  Y+L V+ K I+D+   N TRF +I +++  S GK  TSL     +KPGAL   LE
Sbjct: 239 AAADVYQLPVIEKNIEDI-ANNTTRFIIIGQQTSTSTGKDKTSLVVSTGNKPGALHRTLE 297

Query: 557 VFHKKGFNLRKLESRPAGTGLGDYVFFVEVE 587
            F + G ++  +ESRP+  GL DYVFF++V+
Sbjct: 298 PFARFGVDMVNIESRPSHQGLWDYVFFIDVQ 328


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: 390
Number of extensions: 18
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 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