GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Thermovibrio ammonificans HB-1

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate WP_013537316.1 THEAM_RS02845 aminotransferase class I and II

Query= BRENDA::Q56232
         (385 letters)



>NCBI__GCF_000185805.1:WP_013537316.1
          Length = 369

 Score =  208 bits (529), Expect = 2e-58
 Identities = 129/372 (34%), Positives = 195/372 (52%), Gaps = 19/372 (5%)

Query: 11  MKPSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGI 70
           ++P   + V  +A EL ++G +++ L  GEPD   PE VK  A   L + + KY P  GI
Sbjct: 6   IEPFYVMQVLERAKELEKRGREVIHLEIGEPDLPVPERVKRKAAELLTETELKYTPATGI 65

Query: 71  PELREALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPE 130
           P+L+EA+AE +     + V PE+ +VT G    L    + +     E+    P +  Y  
Sbjct: 66  PKLKEAIAEFYYSRYRVVVEPEQVVVTPGSSPGLVAALKTVSRLVGEISFTDPGYPCYKN 125

Query: 131 MVRFAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALA 190
           +++  G   V +   PE  F   P +V       T AL+VNSP NP+GAVY K  LE L+
Sbjct: 126 ILKVLGEEGVALPVGPENSFKVRPFQV------NTPALIVNSPANPSGAVYTKRELEKLS 179

Query: 191 RLAVEHDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMTGWRIGYACGPK 250
           + A     +L+SDEIY  L Y GE          + + VNG +K F MTGWR+G+     
Sbjct: 180 KRA-----FLISDEIYHGLTY-GEEAPSALEVTRNCIVVNGFSKFFLMTGWRVGWLIASP 233

Query: 251 EVIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTAL 310
           ++++ + ++   +  +P T++Q A +E  + +  S   ++   + +R+R+++LL GL  +
Sbjct: 234 DMVEPINAILQNTVIAPPTLSQLAAVECFSEEVLSE--LQENVKVFRKRKEILLNGLKEI 291

Query: 311 GLKA-VRPSGAFYVLMDTSPIAPDEVRAAERLLE-AGVAVVPGTDFAAFG---HVRLSYA 365
           G K  V P GAFY+  D SP   D  + A  LLE   VAV PG DF   G    VR S+ 
Sbjct: 292 GFKVPVEPKGAFYIWADASPFTEDSFKFAFELLERTSVAVTPGRDFGYNGTEKFVRFSFC 351

Query: 366 TSEENLRKALER 377
           T  E + +ALER
Sbjct: 352 TETEKILEALER 363


Lambda     K      H
   0.317    0.133    0.379 

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: 386
Number of extensions: 30
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 385
Length of database: 369
Length adjustment: 30
Effective length of query: 355
Effective length of database: 339
Effective search space:   120345
Effective search space used:   120345
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 10 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