GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysN in Dechlorosoma suillum PS

Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate Dsui_0420 Dsui_0420 transcriptional regulator with HTH domain and aminotransferase domain

Query= BRENDA::Q72LL6
         (397 letters)



>FitnessBrowser__PS:Dsui_0420
          Length = 469

 Score =  155 bits (391), Expect = 3e-42
 Identities = 117/339 (34%), Positives = 166/339 (48%), Gaps = 19/339 (5%)

Query: 28  LTQRPGILSFAGGLPAPELFPKEEAAEAAARILREKGEVALQ-YSPTEGYAPLRAFVAE- 85
           L   P  L    G   PE +  +E      R L  + EV L  Y    G+APLR  V   
Sbjct: 108 LEDSPNRLKVGVGWLPPE-WHDQEGVRRQLRALARRDEVKLTCYGTPLGFAPLREQVRLK 166

Query: 86  ----WIGVRPEEVLITTGSQQALDLVGKVFLDEGSPVLLEAPSYMGAIQAFRLQGPRFLT 141
                I  +P +++++ G+ Q LDL+ ++ L  G  V ++ P Y       RL G + + 
Sbjct: 167 LADLGIAAQPGQIMLSHGATQGLDLLIRLLLKPGDCVFVDDPGYWNLFANLRLHGVQLVG 226

Query: 142 VPAGEEGPDLDALEEVLKRERPRFLYLIPSFQNPTG-GLTPLPARKRLLQMVMERGLVVV 200
           VP G++GPD  ALE +L   RPR  +     QNPT   L+P  A  R+LQ+  +   ++V
Sbjct: 227 VPWGQDGPDPQALESLLAEHRPRAFFTHSVLQNPTACNLSPANA-FRILQLAEKHDFLLV 285

Query: 201 EDDAYRELYFGEA-RLPSLFELAREAGYPGVIYLGSFSKVLSPGLRVAFAVAHPEALQKL 259
           EDD Y + + G A RL +L +L R      V+Y+GSFSK LS  LRV F    P+ +  L
Sbjct: 286 EDDTYGDFHPGGATRLSTLDQLQR------VVYVGSFSKTLSANLRVGFVAGRPDLMAAL 339

Query: 260 VQAKQGADLHTPMLNQMLVHELLKEG-FSERLERVRRVYREKAQAMLHALDREVPKEVRY 318
              K  + + T  + + LV+E+L  G + + LER+    RE A   L  L+R V  E  Y
Sbjct: 340 TDVKIVSCVSTSEVAEQLVYEMLTAGHYRKYLERIHGRLREAADKTLRLLER-VGMEA-Y 397

Query: 319 TRPKGGMFVWMELPKGLSAEGLFRRALEENVAFVPGGPF 357
             P GGMFVW   P    A  L  +A   ++   PG  F
Sbjct: 398 AEPAGGMFVWARAPGLEDAARLATQAAAADIMLAPGHIF 436


Lambda     K      H
   0.320    0.139    0.403 

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: 462
Number of extensions: 25
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: 397
Length of database: 469
Length adjustment: 32
Effective length of query: 365
Effective length of database: 437
Effective search space:   159505
Effective search space used:   159505
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