GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Pseudomonas fluorescens GW456-L13

Align alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate PfGW456L13_3206 Aspartate aminotransferase (EC 2.6.1.1)

Query= BRENDA::D2Z0I0
         (402 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3206
          Length = 396

 Score =  154 bits (389), Expect = 4e-42
 Identities = 113/375 (30%), Positives = 184/375 (49%), Gaps = 17/375 (4%)

Query: 28  LRREGEDIVDLGMGNPDIPPSQHIIDKLCEVANRPNVHGYSASKGIPRLRKAICDFYKRR 87
           LR +GEDI+ L +G+PD    Q I+    +     N H Y+  +G   LR+AI   +++R
Sbjct: 27  LREQGEDILLLSVGDPDFDTPQPIVQGAIDSLLNGNTH-YAEVRGKRALREAIARRHQQR 85

Query: 88  YGVELDPERNAIMTIGAKEGYSHLMLAMLEPGDTVIVPNPTYPIHYYAPIICGGDAISVP 147
            G  +  ++  ++  GA+     +   +L PGD VIV  P Y  +      CG   + VP
Sbjct: 86  SGQSVSADQVTVLA-GAQCALFSVAQCVLNPGDEVIVAEPMYVTYEAVFGACGAVVVPVP 144

Query: 148 ILPEEDF---PEVFLRRLYDLIKTSFRKPKAVVLSFPHNPTTLCVDLEFFQEVVKLAKQE 204
           +  E  F   PE    R+         + +A+ L+ PHNP+   +    +  + +L    
Sbjct: 145 VRSENGFRVLPEDVAARITP-------RTRALALNSPHNPSGASLPRSTWAALAELCIAH 197

Query: 205 GIWIVHDFAYADLGFDG-YTPPSILQVEGALDVAVELYSMSKGFSMAGWRVAFVVGNEML 263
            +W++ D  Y++L F+G +  P+ L   G  +    L S+SK  +M GWRV +VV    L
Sbjct: 198 DLWLISDEVYSELLFEGEHVSPASLP--GMAERTATLNSLSKSHAMTGWRVGWVVAPPSL 255

Query: 264 IKNLAHLKSYLDYGVFTPIQVASIIALESPYEVVEKNREIYRRRRDVLVEGL-NRVGWEV 322
             +L +L   + YG    IQ A+++ALES    +E  RE YR+RRD++ + L +  G   
Sbjct: 256 AAHLENLALCMLYGSPDFIQDAAVVALESNLPELEAMREAYRQRRDLVCDSLADCPGVRA 315

Query: 323 KKPKGSMFVWAKVPEEVGMNSLDFSLFLLREAKVAVSPGIGFGEYGEGYVRFALVENEHR 382
            KP G MFV   +  + G+++  F+  LL    V+V  G  FG    G++R  LV     
Sbjct: 316 LKPDGGMFVMLDI-RQTGLSAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVVGAEP 374

Query: 383 IRQAVRGIKKALDKI 397
           +R A + I +   ++
Sbjct: 375 LRDACQRIARCAQEL 389


Lambda     K      H
   0.322    0.141    0.425 

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: 352
Number of extensions: 21
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: 402
Length of database: 396
Length adjustment: 31
Effective length of query: 371
Effective length of database: 365
Effective search space:   135415
Effective search space used:   135415
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 (21.9 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