GapMind for Amino acid biosynthesis

 

Alignments for a candidate for aro-dehydratase in Methylohalobius crimeensis 10Ki

Align arogenate dehydratase (EC 4.2.1.91) (characterized)
to candidate WP_022947855.1 H035_RS0104750 prephenate dehydratase

Query= BRENDA::Q9SSE7
         (381 letters)



>NCBI__GCF_000421465.1:WP_022947855.1
          Length = 361

 Score =  150 bits (378), Expect = 7e-41
 Identities = 107/334 (32%), Positives = 164/334 (49%), Gaps = 32/334 (9%)

Query: 45  RIVTVLASLRENDANGRDNSVRAMEVKKIFEDSPLLPKPLSSNQLTESVSNGSRVRVAYQ 104
           R   VL  ++  +    D+ V     ++I      L KPL               +VA+ 
Sbjct: 53  REAEVLRRIKAKNPGPLDDDVAVRIFREIMSACLALEKPL---------------QVAFL 97

Query: 105 GVRGAYSESAAEKAYPNC-EAVPCEEFDTAFEAVERWLVDRAVLPIENSLGGSIHRNYDL 163
           G  G +++ AA K +     A+P    D  F AV        V+P+ENS  G +    D 
Sbjct: 98  GPEGTFTQQAAYKHFGQAIAALPLPAVDEIFRAVAGGACGYGVVPVENSTEGVVTHTLDS 157

Query: 164 LLRHNLHIVGEVKLAVRHCLLANHGVNIEDLRRVLSHPQALAQCENTLTKL--GLVREAV 221
            L  +L I GEV L + H L++     ++ +  V SH Q+LAQC   L +      R  V
Sbjct: 158 FLNTSLLISGEVVLRIHHNLMSRRA-ELQAIEEVFSHQQSLAQCREWLDRFLPHAKRTPV 216

Query: 222 DDTAGAAKQIAFENLNDAAAVASEKAAKIYGLNIVAKDIQDDCDNVTRFLMLAREPIIPG 281
              A  A+  A   + ++AA+A E AA++Y L+++   I+DD DN TRFL++ ++P+ P 
Sbjct: 217 SSNAEGARLAAI--VPNSAAIAGEVAARLYELDVLESSIEDDPDNTTRFLVIGKQPVGPT 274

Query: 282 TNRLFKTSIVFSLEEGPGVLFKALAVFALRQINLTKIESRPLRKHPLRASGGLKYFDYLF 341
            +   KTS+V S    PG L++ L  FA  +I+++KIESRP R+           ++Y+F
Sbjct: 275 GDD--KTSLVVSTRNAPGALYRLLQPFADHRISMSKIESRPSRQ---------GMWEYVF 323

Query: 342 YVDFEASMADEVAQNALRHLEEFATFLRVLGSYP 375
           ++D E    D     AL  LEE A  ++ LGSYP
Sbjct: 324 FIDIEGHRDDVRVTEALTALEERAQMVKWLGSYP 357


Lambda     K      H
   0.319    0.134    0.384 

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: 276
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: 381
Length of database: 361
Length adjustment: 30
Effective length of query: 351
Effective length of database: 331
Effective search space:   116181
Effective search space used:   116181
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 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