GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Burkholderia phytofirmans PsJN

Align Aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.78 (characterized)
to candidate BPHYT_RS00155 BPHYT_RS00155 aminotransferase

Query= SwissProt::Q8KDS8
         (400 letters)



>FitnessBrowser__BFirm:BPHYT_RS00155
          Length = 384

 Score =  165 bits (417), Expect = 2e-45
 Identities = 111/363 (30%), Positives = 189/363 (52%), Gaps = 16/363 (4%)

Query: 38  DVVSLSAGEPDFPTPENVCEAGIEAIRKGFTRYTANSGIPELKKAIIRKLQRDNGLEY-A 96
           D ++LS G P+F     + +   +A+R G  +Y   +GI  L++A+  K+    G+ Y  
Sbjct: 30  DALNLSQGAPNFAPDAKLIDGVAQAMRAGHNQYAPMAGIAALREALADKVATLYGVRYDP 89

Query: 97  EDEIIVSNGGKQALANTFLALCDEGDEVIVPAPYWVSFPEMARLAEATPVIVETSIETGY 156
             E+ V     + L +T  AL   GDEVI   P + S+  + RL  ATPV ++ S++  +
Sbjct: 90  ASEVTVIASASEGLYSTISALVHPGDEVIYFEPSFDSYGPIVRLQGATPVPIKLSLDD-F 148

Query: 157 KMTPEQLAAAITPKTRILVLNSPSNPSGAVYNEAEVRALMQVIEGKEIFVLSDEMYDMIC 216
           ++  +++AAAITPKTR+++ N+P NP+  V++EA+V  L  V    +I +L+DE+Y+ + 
Sbjct: 149 RVNWDEVAAAITPKTRMIITNTPHNPTATVFSEADVERLKAVTRNTDIVILADEVYEHVV 208

Query: 217 YGGVRPFSPARIPEMKPWVIVSNGTSKSYSMTGWRIGYLAAPKWIINACDKIQSQTTSNA 276
           + G +  S A   E+    ++ +   KSY +TGWR+GY  AP  +++   K+      +A
Sbjct: 209 FDGAKHQSMACHSELAERSVIVSSFGKSYHVTGWRVGYCLAPAALMDEIRKVHQFMVFSA 268

Query: 277 NSIAQKAAVAALDGDQSIVEQRRAEFEKRRDFMFRELNTISGIECTLPEGAFYIFPSIKG 336
           ++  Q A V AL   +S +    A ++K+RD +   L   S  E    EG+F++    +G
Sbjct: 269 DTPMQYAFVDALANRESYL-GLSAFYQKKRDLLAEALRD-SRFELLPSEGSFFMLARFRG 326

Query: 337 LLGKTFGGKVMKDSTDVAEYLLTEHYVATVPGDAF---GAPENL-RLSYAASIEELAEAV 392
              ++         +D    L+ +  VAT+P  AF   G    L RLS++     L E  
Sbjct: 327 FSDES--------DSDFVLRLIRDARVATIPLSAFYTDGTDSGLIRLSFSKDDATLIEGA 378

Query: 393 NRI 395
            R+
Sbjct: 379 RRL 381


Lambda     K      H
   0.316    0.132    0.376 

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: 316
Number of extensions: 17
Number of successful extensions: 3
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: 400
Length of database: 384
Length adjustment: 31
Effective length of query: 369
Effective length of database: 353
Effective search space:   130257
Effective search space used:   130257
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 (21.6 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