GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Beijerinckia mobilis UQM 1969

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate WP_034996772.1 DL88_RS12710 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= BRENDA::Q56232
         (385 letters)



>NCBI__GCF_000745425.1:WP_034996772.1
          Length = 389

 Score =  164 bits (416), Expect = 3e-45
 Identities = 114/383 (29%), Positives = 176/383 (45%), Gaps = 11/383 (2%)

Query: 1   MRGLSRRVQAMKPSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQG 60
           +RG S    AM P   + +  +A +  R+G ++V +  GEP   TP  V+EA +  LA+G
Sbjct: 5   LRGRSSSRSAMAPFLALDILNQATQREREGQNIVHMEVGEPGAATPALVREAVQEELARG 64

Query: 61  KTKYAPPAGIPELREALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIV 120
           +  Y    G P LR  +A  +R   G+ V PE   VT+G        F A  D G  + V
Sbjct: 65  RIGYTEALGRPSLRARIARHYRETYGVEVPPERVAVTIGSSGGFMLAFLAGFDAGARIGV 124

Query: 121 LSPYWVSYPEMVRFAGGVVVEVETLPEEGFVPDPERVRRAITPR-TKALVVNSPNNPTGA 179
            SP + +Y  +    G   V +ET      V     +      +    L++ SP NPTG 
Sbjct: 125 QSPGYPAYRNIFDALGLEAVVIETNGASRHVVTAAMIEATHAEKPLDGLLLMSPANPTGT 184

Query: 180 VYPKEVLEALARLAVEHDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMT 239
           +   E L+A+  +        VSDE+Y  L Y GE         +  +  N  +K + MT
Sbjct: 185 MMSPEDLQAVCAVCDRLGITFVSDEVYHGLTY-GEPAETALKFSDRVIVANSFSKYYCMT 243

Query: 240 GWRIGYACGPKEVIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRR 299
           GWR+G+   P+E ++ +  +      S   ++Q A   A      +R  +++ +  Y   
Sbjct: 244 GWRVGWLIVPEEFVRPIERLQQNLAISVPYLSQVAAEAAFD----ARDELQLIKAGYAAN 299

Query: 300 RDLLLEGLTALGLKAVRP-SGAFYVLMDTSPIAPDEVRAAERLL-EAGVAVVPGTDF--- 354
           R+ LL  L  +GL    P  GAFY+  D S    D +  + R+L E G+AV PG DF   
Sbjct: 300 RNFLLNSLPQIGLSEFHPVDGAFYIYADVSRFTNDSLDFSRRMLDETGIAVTPGLDFDRN 359

Query: 355 AAFGHVRLSYATSEENLRKALER 377
                +RLS+A  E ++ +A+ R
Sbjct: 360 RGNSFIRLSFAGPERDMVEAVSR 382


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: 340
Number of extensions: 19
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: 385
Length of database: 389
Length adjustment: 30
Effective length of query: 355
Effective length of database: 359
Effective search space:   127445
Effective search space used:   127445
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 Jul 25 2024. The underlying query database was built on Jul 25 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