GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Cupriavidus basilensis 4G11

Align [LysW]-aminoadipate semialdehyde/glutamate semialdehyde transaminase; EC 2.6.1.118; EC 2.6.1.124 (uncharacterized)
to candidate RR42_RS16955 RR42_RS16955 acetylornithine aminotransferase

Query= curated2:Q7SI94
         (388 letters)



>FitnessBrowser__Cup4G11:RR42_RS16955
          Length = 395

 Score =  189 bits (480), Expect = 1e-52
 Identities = 120/363 (33%), Positives = 195/363 (53%), Gaps = 16/363 (4%)

Query: 17  KGEGQYVWDEKNNKYLDMHAGHGVAFLGHRNKVIIDHLKKQMEEISTLSLAFDTPIREEM 76
           +G+G ++ D    +YLD   G  V  LGH N+ +ID L  Q +++   S AF     E M
Sbjct: 24  EGKGSWLTDHNGKRYLDFVQGWAVNCLGHSNQAMIDALVDQSKKLFNPSPAF---YNEPM 80

Query: 77  IKELDELKPED-LDNLFLLNSGSEAVELALKIARKITKRRK-----IVAFKNSFHGRSMG 130
           ++   +L      D +F  NSG+EA E A+K+ARK  ++ K     I+   +SFHGR++ 
Sbjct: 81  LRLARQLTDASCFDKVFFANSGAEANEGAIKLARKWGRKHKNGAFEIITMDHSFHGRTLA 140

Query: 131 ALSVTWNKKYREPFEPLIGPVEFLEYNNVDSLKSITED-TAAVIVEPVQGEGGVIPAKKE 189
            +S +    +   F P +      + N++ S++ +  D T A+++EPVQGEGGVIPA +E
Sbjct: 141 TMSASGKAGWDTIFAPQVPGFPKADLNDLASVEKLINDKTVAIMLEPVQGEGGVIPASRE 200

Query: 190 FVKSLREVTEKVNALLIIDEVQTGFGRTGKIWAYQHFDIKPDILTAGKAIGGGFPVSAVF 249
           F++ LR++ ++   L I+DEVQTG GR G ++AY+   ++PDI+T GK IGGG P++A+ 
Sbjct: 201 FMQGLRKLADQHKLLFIVDEVQTGCGRCGTMFAYELSGVEPDIMTLGKGIGGGVPLAALL 260

Query: 250 LPNWISEKIEEGDHGSTYGGNPLAAAAVTAACKVAKSEKIAEQAQKKGELFMRILKEKLE 309
               ++   E GD G TY GNP+  A  +A      +    +  Q KG      L     
Sbjct: 261 CKAEVA-SFEAGDQGGTYNGNPVMTAVGSAVISQLTAPGFLQSVQDKGAYLREQLLALTS 319

Query: 310 DFKIVREIRGLGLMIGIDLK--VNPSIA--IKVLQDEKVLSLKAGLTTIRFLPPYLITQS 365
           +F +  E RG GL+  + L   + P +    + +Q + +L        +RF+P   +T  
Sbjct: 320 EFGLGGE-RGEGLLRALVLNKDIGPQLVEEARDMQPQGLLLNSPRPNLLRFMPALNVTIE 378

Query: 366 DME 368
           +++
Sbjct: 379 EID 381


Lambda     K      H
   0.317    0.136    0.386 

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: 324
Number of extensions: 17
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: 388
Length of database: 395
Length adjustment: 31
Effective length of query: 357
Effective length of database: 364
Effective search space:   129948
Effective search space used:   129948
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