GapMind for Amino acid biosynthesis

 

Alignments 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)



>FitnessBrowser__Dyella79:N515DRAFT_1431
          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 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