GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Cupriavidus basilensis 4G11

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate RR42_RS05770 RR42_RS05770 aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Cup4G11:RR42_RS05770
          Length = 395

 Score =  168 bits (426), Expect = 2e-46
 Identities = 117/376 (31%), Positives = 180/376 (47%), Gaps = 18/376 (4%)

Query: 12  KPSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIP 71
           K   T+     AL   R  V+L     G PDFD    + +A   A+  G  +Y P AG+P
Sbjct: 24  KVGTTIFTVMSALAAERNAVNL---GQGFPDFDCDPKIVDAVAHAMRSGLNQYPPMAGVP 80

Query: 72  ELREALAEKFRRENGLSVT-PEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPE 130
           +LR+A+A K  +  G +     E  VT G  Q +       + PGDEVIVL P + SY  
Sbjct: 81  KLRQAIAGKIGKLYGHAYDWDSEITVTAGATQGILTTILCAVHPGDEVIVLEPCYDSYIP 140

Query: 131 MVRFAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALA 190
            +  AGG VV V        +P  +R+  AITPRT+ L++N+P+NPTG ++    ++ LA
Sbjct: 141 AIEMAGGKVVSVALDAPHFHIPF-DRLAAAITPRTRMLLINTPHNPTGTIWRAGDMDRLA 199

Query: 191 RLAVEHDFYLVSDEIYEHLLYEGEHFSPGRVAPE---HTLTVNGAAKAFAMTGWRIGYAC 247
            L    D  L+SDE+YEH++++G+        PE    +  V+   K + +TGW++GY  
Sbjct: 200 GLLAGTDILLLSDEVYEHMVFDGQPHQSVSRHPELARRSFVVSSFGKTYHVTGWKVGYVA 259

Query: 248 GPKEVIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGL 307
            P  +      V   +  + +T  Q    + + +      ++++A   Y+ +RD    GL
Sbjct: 260 APAALSAEFRKVHQFNVFTVNTPVQHGLADYMAD---PAPYLDLA-AFYQAKRDFFRAGL 315

Query: 308 TALGLKAVRPSGAFYVLMDTSPIAPDEVRAAERLL--EAGVAVVPGTDFAA----FGHVR 361
            A   K +   G ++  +D S I+          L  E GVA +P + F +     G VR
Sbjct: 316 AATRFKLLPSDGTYFQCVDYSAISDMSEADFSMWLTREIGVAAIPVSAFYSQPRESGVVR 375

Query: 362 LSYATSEENLRKALER 377
             +A  EE L  AL R
Sbjct: 376 FCFAKKEETLALALAR 391


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: 342
Number of extensions: 19
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: 385
Length of database: 395
Length adjustment: 31
Effective length of query: 354
Effective length of database: 364
Effective search space:   128856
Effective search space used:   128856
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