GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Thermomonospora curvata DSM 43183

Align succinyldiaminopimelate transaminase (EC 2.6.1.17); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_012851519.1 TCUR_RS05675 succinyldiaminopimelate transaminase

Query= BRENDA::Q82IK5
         (364 letters)



>NCBI__GCF_000024385.1:WP_012851519.1
          Length = 363

 Score =  497 bits (1279), Expect = e-145
 Identities = 241/360 (66%), Positives = 279/360 (77%), Gaps = 4/360 (1%)

Query: 8   LPTFPWDKLEPYKARAAAHPDGIVDLSVGTPVDPVPELIQKALVAAADSPGYPTVWGTPE 67
           LP FPWD+L PYK  AA HP G+VDLSVGTPVDP PE I++AL  AAD+PGYP  +GT  
Sbjct: 4   LPDFPWDRLAPYKQIAARHPGGLVDLSVGTPVDPTPEPIRRALAEAADAPGYPQTYGTAA 63

Query: 68  LRDALTGWVERRLGARGVTHHHVLPIVGSKELVAWLPTQLGLGPGDKVAHPRLAYPTYEV 127
           LR+A  GW+ RRLG  G     VLP++G+KELVAWLPT LG GPGD+V  P LAYPTY+V
Sbjct: 64  LREAAAGWLRRRLGVAGADPAAVLPVIGTKELVAWLPTLLGCGPGDRVVFPELAYPTYDV 123

Query: 128 GARLARADHVVYDDPTELDPTGLKLLWLNSPSNPTGKVLSKAELTRIVAWAREHGILVFS 187
           GARLA A+ V  D    L P   KLLW+NSPSNPTGKVL    L ++VAWARE G+LV S
Sbjct: 124 GARLAGAEPVAADGLLRLGPLRPKLLWINSPSNPTGKVLPAEHLRKVVAWARERGVLVAS 183

Query: 188 DECYLELGWEAD----PVSVLHPDVCGGSYEGIVSVHSLSKRSNLAGYRAAFLAGDPAVL 243
           DECY+EL WE D    PVS+LHP+VC GS+EG+++VHSLSKRSNLAGYRA F+ GDPA++
Sbjct: 184 DECYIELAWEDDPAKQPVSILHPEVCEGSHEGLLAVHSLSKRSNLAGYRAGFVTGDPALV 243

Query: 244 GPLLQIRKHGGMMTSAPTQAAVVAALGDDAHVREQRERYAARRTALRDALLSHGFRIEHS 303
             LL++RKH GMM  AP QAA+  A GDDAHV EQR RYA RR  LR+AL  HGFRI+HS
Sbjct: 244 KRLLEVRKHAGMMVPAPVQAAMTVAYGDDAHVDEQRARYARRRAVLREALERHGFRIDHS 303

Query: 304 EASLYLWATRGESCWDTVAHLADLGILVAPGDFYGSAGEQFVRVALTATDERVAAAVRRL 363
           EASLYLWATR E CWDTVAHLA+LGI VAPGDFYG+AG + VRVA TATDER+ AA +RL
Sbjct: 304 EASLYLWATRDEPCWDTVAHLAELGISVAPGDFYGAAGSRHVRVAFTATDERIEAAAQRL 363


Lambda     K      H
   0.319    0.135    0.420 

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: 598
Number of extensions: 23
Number of successful extensions: 2
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: 364
Length of database: 363
Length adjustment: 29
Effective length of query: 335
Effective length of database: 334
Effective search space:   111890
Effective search space used:   111890
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 (21.7 bits)
S2: 49 (23.5 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