GapMind for Amino acid biosynthesis

 

Aligments for a candidate for aro-dehydratase in Dyella japonica UNC79MFTsu3.2

Align arogenate dehydratase (EC 4.2.1.91) (characterized)
to candidate N515DRAFT_1431 N515DRAFT_1431 chorismate mutase

Query= BRENDA::Q9SGD6
         (413 letters)



>lcl|FitnessBrowser__Dyella79:N515DRAFT_1431 N515DRAFT_1431
           chorismate mutase
          Length = 362

 Score =  143 bits (360), Expect = 9e-39
 Identities = 115/348 (33%), Positives = 160/348 (45%), Gaps = 31/348 (8%)

Query: 65  GHNSAAARVPGMNLVPIE------KSDSNPLVPQHRHNPLKPLSMTDL-----SPAPMHG 113
           G     ARV G  L  I+      ++    +V      PL    M  L     S      
Sbjct: 31  GWAQEVARVKGAGLSAIDYYRPEREAHVLRMVVDRNRGPLSDTEMVRLFREIMSSCLAQE 90

Query: 114 SNLRVAYQGVPGAYSEAAAGKAYPNCQ-AIPCDQFEVAFQAVELWIADRAVLPVENSLGG 172
             L+V + G  G +SE A  K + +    +P    E  FQ V    AD  V+PVENS  G
Sbjct: 91  DPLKVGFLGPEGTFSEQAVRKHFGHAAYGLPLGSIEEVFQEVAAGHADFGVVPVENSGQG 150

Query: 173 SIHRNYDLLLRHRLHIVGEVQLPVHHCLLALPGVRKEFLTRVISHPQGLAQCEHTLTKLG 232
            I    D+ L     I GE++L VH CL +  G R E + RV +H Q L QC+  L    
Sbjct: 151 MIQITLDMFLTSEATICGEIELRVHQCLHS-QGGRMEDIKRVYAHAQSLQQCKTWLRINL 209

Query: 233 LNVAREAVDDTAGAAEFIASNNLRDTAAIASARAAEIYGLEILEDGIQDDVSNVTRFVML 292
            +V   AV   A AA    + +  D AAIA   A  +YGL+ L  GI+D   N TRF+++
Sbjct: 210 PDVECIAVSSNAEAARM--ARHADDAAAIAGETAGRVYGLKTLATGIEDRADNTTRFLVI 267

Query: 293 AREPIIPRTDRPFKTSIVFAHEKGTSVLFKVLSAFAFRDISLTKIESRPNHNRPIRVVDD 352
            R    P  +   +TS++         L+ VLS FA  D+SL +IESRP H         
Sbjct: 268 GRSLFPPSGND--RTSLLITVNDKPGALYDVLSPFAKHDVSLNRIESRPAH--------- 316

Query: 353 ANVGTAKHFEYMFYVDFEASMAEARAQNALAEVQEFTSFLRVLGSYPM 400
               T K ++Y F++D    + +A  Q A+ E+    + +RVLGSYP+
Sbjct: 317 ----TGK-WQYAFFIDVSGHVQDAPIQAAMQEMGGAAAQVRVLGSYPV 359


Lambda     K      H
   0.317    0.131    0.381 

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: 302
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: 413
Length of database: 362
Length adjustment: 30
Effective length of query: 383
Effective length of database: 332
Effective search space:   127156
Effective search space used:   127156
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.

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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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.

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