GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Pseudarthrobacter sulfonivorans Ar51

Align Probable prephenate dehydrogenase NovF; EC 1.3.1.12; Novobiocin biosynthesis protein F (uncharacterized)
to candidate WP_058929409.1 AU252_RS02695 prephenate dehydrogenase

Query= curated2:Q9L9G2
         (362 letters)



>NCBI__GCF_001484605.1:WP_058929409.1
          Length = 369

 Score =  199 bits (507), Expect = 7e-56
 Identities = 132/358 (36%), Positives = 187/358 (52%), Gaps = 13/358 (3%)

Query: 5   VIIGTGMIGTSIGLALRKQGVDSYLMDTSPVALRIAEAVGAGTAEEP--PETVDLAVVAV 62
           V+IGTG++G SIGL LR +GV  +L D SP    +A  +GAG   +    E  +L VVA 
Sbjct: 17  VVIGTGLLGASIGLGLRGRGVPVFLSDPSPTNQAVAVDIGAGQPLDQLGDEAPELVVVAA 76

Query: 63  PPVHVAPVIASHQSRGTARFYVDVAGVKVSTRRELDALGCDLATVVGGHPLVGRPGSGPL 122
           PP   A V+A   +       VD+A VK +   EL   G DLA  VG HP+ GR  SGP+
Sbjct: 77  PPDVTADVVARALADYPDSVVVDIASVKAAILAELGGRGADLARYVGTHPMAGREKSGPV 136

Query: 123 AARGDLFDGRPWALVPAVGTDAAALNRALELVAACGAIPVVLDAEAHDRAIALGTLVPQI 182
           AARG+LF   PW + P   + AAA+  A  L    GA+     A+ HD A+AL + +PQI
Sbjct: 137 AARGELFTSMPWVVCPGPESSAAAVQTARSLATDLGAVVSQFTADEHDEAVALVSHLPQI 196

Query: 183 ALTLVAARLTEADSGALRLLGSVWSEIPQLVGVDSATSWTQVLAANAAPVVGELEKLSRD 242
             +L+A+RL      AL L G+   ++ ++   D  T W Q+L  NA  VV  L  +  D
Sbjct: 197 MSSLLASRLQGTPLHALSLAGNGLRDVTRIAASD-PTLWVQILGGNAGKVVEILYGVRED 255

Query: 243 LASLLETLRGVADGDGSLAEPDGR--LLEFIQRGIDGSNRVPGRYGIPTETALADVDVSV 300
           L  L+ TL      +  LA P  R  L + I  G  G  R+PG++G P + A + + V V
Sbjct: 256 LNRLIGTL------EEPLA-PGARLDLAQLISEGNAGQARIPGKHGGPPQ-AYSWLTVLV 307

Query: 301 DDRPAELARLFDDVAGAGVVMRGIDISQRPDSPDRTVTISVTPRDAENLLHELRRRKW 358
           DDRP ++A+L  ++   GV +  + +          V +SV P   ++L+  L  R W
Sbjct: 308 DDRPGQIAQLLTEIGEIGVNVEDLRLDHSSGQNVGMVELSVLPNKHDHLIEALNDRGW 365


Lambda     K      H
   0.317    0.135    0.390 

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: 346
Number of extensions: 23
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: 362
Length of database: 369
Length adjustment: 30
Effective length of query: 332
Effective length of database: 339
Effective search space:   112548
Effective search space used:   112548
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: 49 (23.5 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