GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Phaeobacter inhibens BS107

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate GFF1996 PGA1_c20300 aminotransferase

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__Phaeo:GFF1996
          Length = 382

 Score =  155 bits (391), Expect = 2e-42
 Identities = 111/361 (30%), Positives = 179/361 (49%), Gaps = 17/361 (4%)

Query: 30  VISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAV-QLYMKKKADFNYDA 88
           +I + +GQP    P   + A  KA+D +   YT   G   LR+ + QLY +    +N D 
Sbjct: 31  IIHMEVGQPSTGAPVAAREALAKALDHDSLGYTVALGLPALRKRIAQLYGEW---YNVDL 87

Query: 89  ESE-IIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDTTSHGF 147
             E ++IT G+S A   +F  +   GD V +  P YP Y  I++  G  PV ++T+    
Sbjct: 88  NPERVVITPGSSGAFLLSFTALFDSGDRVGIGAPGYPSYRQILHALGLTPVDIETS---- 143

Query: 148 KLTARLI---EDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDEIYS 204
            L  RL    +D    +   +++  P+NPTG  L +  + ++    +G+    +SDEIY 
Sbjct: 144 -LDHRLQPVPQDLTGLDLAGLMVASPANPTGTMLDKPAMAALIDAAQGQGAAFISDEIYH 202

Query: 205 ELTYDRPHYSIATYLRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYNVSCA 264
            + Y+    + A  + D+  VIN  SK  SMTGWR+G++  P+D  + + ++ Q    CA
Sbjct: 203 GIEYEAKAVT-ALEVTDECYVINSFSKYFSMTGWRVGWMVVPEDHVRVVERIAQNMFICA 261

Query: 265 SSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSMGLD-VVKPSGAFYIFPSIKS 323
              SQ AAL A+ +  D+       Y +    + + L   G D +  P GAFY++  +  
Sbjct: 262 PHASQVAALAAM-DCRDELEGNLAVYARNRALMLEGLPKAGFDRIAPPDGAFYVYADVSE 320

Query: 324 FGMTSFDFSMALLEDAGVALVPGSSFS-TYGEGYVRLSFACSMDTLREGLDRLELFVLKK 382
               S  F+  +L++AGVA+ PG  F    G   +R S+A +   + EGL RL  F+  +
Sbjct: 321 LTHDSRAFAQEILDEAGVAVTPGLDFDPKRGATTLRFSYARATADIEEGLTRLAAFMAAR 380

Query: 383 R 383
           R
Sbjct: 381 R 381


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: 343
Number of extensions: 27
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: 382
Length adjustment: 30
Effective length of query: 363
Effective length of database: 352
Effective search space:   127776
Effective search space used:   127776
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