GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Paraburkholderia bryophila 376MFSha3.1

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate H281DRAFT_02907 H281DRAFT_02907 arginine:pyruvate transaminase

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__Burk376:H281DRAFT_02907
          Length = 395

 Score =  193 bits (490), Expect = 8e-54
 Identities = 118/360 (32%), Positives = 186/360 (51%), Gaps = 7/360 (1%)

Query: 25  AQHEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADF 84
           A   DVI L++G PDF TP  +   A  A+    T Y+  +G   LR A+     +    
Sbjct: 29  ANGNDVIVLSVGDPDFATPAPIVERAIDALRGGDTHYSAVSGRDPLRAAIAEEQARMTGC 88

Query: 85  NYDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAK--PVIVDT 142
              A + +I+T GA   + A    +L  GDEVI+P P+Y  YE  +   GA   PV VD 
Sbjct: 89  TVSA-ANVILTAGAQNGVFATSLCLLEAGDEVIVPEPMYLTYEACVRAAGATLVPVPVDP 147

Query: 143 TSHGFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDEI 202
            +  F L    +E A+TP TK +    P NPTGV +   +L+ IA L    +++VLSDE+
Sbjct: 148 -ARAFHLDCDALERAVTPRTKAIFFATPCNPTGVVMPRADLERIARLACEHDLWVLSDEV 206

Query: 203 YSELTYDRPHYSIATY--LRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYN 260
           Y++LT++R H SI +   + ++T+ +  LSKSH+M GWR+G+   P  + +H+ ++    
Sbjct: 207 YADLTFEREHVSIMSLPGMAERTVTLGSLSKSHAMAGWRVGWAIGPTQLIEHMGRLALAM 266

Query: 261 VSCASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSM-GLDVVKPSGAFYIFP 319
           +       Q+AAL A+         MR+ Y++R D V++RL  +  L  + P    ++  
Sbjct: 267 LYGLPGFIQQAALTALQEKSSIVAQMRDIYRRRRDVVFERLSRVPRLRCLLPEAGMFMMV 326

Query: 320 SIKSFGMTSFDFSMALLEDAGVALVPGSSFSTYGEGYVRLSFACSMDTLREGLDRLELFV 379
            +   G+ + DF+  L    GV+++  S+F     G+VRL F      L E  +R+  FV
Sbjct: 327 DVSGTGLDTVDFTWQLFRAQGVSVLDASAFGETANGFVRLGFVVDEARLAEACERIAAFV 386


Lambda     K      H
   0.319    0.135    0.388 

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: 292
Number of extensions: 15
Number of successful extensions: 6
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: 393
Length of database: 395
Length adjustment: 31
Effective length of query: 362
Effective length of database: 364
Effective search space:   131768
Effective search space used:   131768
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 (21.8 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