GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pseudomonas simiae WCS417

Align Aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.79 (characterized)
to candidate GFF4517 PS417_23120 aminotransferase

Query= SwissProt::A3PMF8
         (400 letters)



>FitnessBrowser__WCS417:GFF4517
          Length = 382

 Score =  160 bits (406), Expect = 4e-44
 Identities = 113/371 (30%), Positives = 177/371 (47%), Gaps = 18/371 (4%)

Query: 28  AAGRDVIGLGAGEPDFDTPDNIKAAAKRAIDAGRTKYTAVDGIPELKRAICEKFERENGL 87
           AA    + L  G PDF  P  +  A  + I  G  +Y  + G+P L++ +  K  R  G 
Sbjct: 21  AAETGALNLSQGFPDFSGPQGLLDAVGKHIALGHNQYAPMTGLPVLRQQVAAKIARSYGA 80

Query: 88  KY-TPAQVTVGTGGKQILYNALVATLNPGDEVIIPAPYWVSYPDMVLLAGGTPVSVAAGM 146
                ++VT+  G  + ++ A+ A +  GDEVI+  P + SY   V LAGG  V V   +
Sbjct: 81  TVDADSEVTITPGATEAIFCAIQAVIRNGDEVIVFDPSYDSYEPSVELAGGRCVHVQLSL 140

Query: 147 ETGFKLTPEQLEAAITPRTKWFIFNSPSNPTGAAYTRAELAALCEVLMRHPQVWIMSDDM 206
            +GF L  E+++AA++PRT+  I N+P NPTGA  +RAEL  L E L+R   ++++SD++
Sbjct: 141 -SGFALDFEKIKAALSPRTRMIILNTPHNPTGALISRAELDQLAE-LIRDRDIYLVSDEV 198

Query: 207 YEHLVFDDFDFTTPAQIEPGLYDRTLTCNGVSKAYCMTGWRIGYAAGPVELIRAMGTIQS 266
           YEHLVFD     +    E  LY R    +   K Y +TGW+ GY   P  L   +  +  
Sbjct: 199 YEHLVFDGVAHVSVLAHEE-LYPRAFVVSSFGKTYHVTGWKTGYVVAPPALTAELRKVHQ 257

Query: 267 QSTSNPCSIAQYAALEALSGPQEFLATNREAFQRRRDLVVSMLNEAKGVTCPNPEGAFYV 326
                  +  QYA  + ++   E +      +Q +RDL   +L  A   +     G ++ 
Sbjct: 258 YVNFCGVTPLQYALADFMAEHPEHVEELPAFYQAKRDLFCDLL-AASRFSFTRVTGTYFQ 316

Query: 327 YPDISGCIGKTSAGGAKITDDEAFASALLEETGVAVVFGAAFGLSPN-----FRISYATA 381
             D S              DD A +  +  E GVA +  + F  +P       R+ +A  
Sbjct: 317 LVDYSQI--------RPDLDDVAMSLWMTREHGVATIPVSVFYQTPPQGQRLVRLCFAKR 368

Query: 382 DEVLREACARI 392
           +E LR+A  ++
Sbjct: 369 EETLRQAAEKL 379


Lambda     K      H
   0.318    0.134    0.399 

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: 398
Number of extensions: 19
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: 400
Length of database: 382
Length adjustment: 31
Effective length of query: 369
Effective length of database: 351
Effective search space:   129519
Effective search space used:   129519
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 (21.7 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