GapMind for Amino acid biosynthesis

 

Alignments for a candidate for trpE in Pedobacter sp. GW460-11-11-14-LB5

Align Anthranilate synthase component 1; AS; ASI; EC 4.1.3.27 (uncharacterized)
to candidate CA265_RS14515 CA265_RS14515 aminodeoxychorismate synthase component I

Query= curated2:Q08653
         (461 letters)



>FitnessBrowser__Pedo557:CA265_RS14515
          Length = 418

 Score =  184 bits (466), Expect = 6e-51
 Identities = 124/367 (33%), Positives = 187/367 (50%), Gaps = 19/367 (5%)

Query: 95  DELPSF----RGGAVGFVSYDYISYIEKVKVKASV---FPTFYFVVPEHLIIFDHLKNNV 147
           D+L SF    +    GF  YD  + IE +    S    FP  YF VP++LI F      V
Sbjct: 60  DQLKSFYALHKQWIFGFFGYDLKNEIEDLHSNNSDHLNFPDLYFFVPKYLIAFKKGNAEV 119

Query: 148 FIISDSPEELTSKVLSPFEEKPEKNVFVTEPESNFEREQFYKVVEKAKKYIVEGDIFQVV 207
            I    PE + +++ S F+ K E      +      ++Q+ + VE  + +I+ GDI++V 
Sbjct: 120 LI---GPESILAEIDS-FQLKTEIQSKKAKVAQRLSKDQYVQKVEALRDHIIRGDIYEVN 175

Query: 208 LSQAFTFKTT-LDPFYIYRALRMINPSPYMFYLKFGDTVVLGSSPETMAKVEGDKATVKP 266
             Q F  +   +DP   + AL  ++P+P+  Y K     +L ++PE      G K T +P
Sbjct: 176 FCQEFFAENAEIDPVQTFEALNSVSPTPFAGYFKVQGNYILSATPERFLCKRGSKLTSQP 235

Query: 267 IAGTRPRGRTVEEDLKLERELLNDEKEIAEHVMLVDLGRNDLGRVCKEGTVRVEKKMVIE 326
           I GT  R     ED  ++ +L ND KE AE+VM+VDL R+DL +   +G+V V++   I 
Sbjct: 236 IKGTAKRSLDPMEDEAIKLQLRNDIKEQAENVMIVDLVRHDLTKSAVKGSVTVDELFGIY 295

Query: 327 RYSHVMHIVSQVSGELKDDKDAVDVFEATFPAGTVSGAPKVRAMEIIEELEPTPRGPYAG 386
            +  V  ++S +S EL      +D  +  FP G+++GAPKV+AM++IEE E T RG Y+G
Sbjct: 296 SFPQVHQMISTISCELNPAIHFIDAIKNAFPMGSMTGAPKVKAMKLIEEYEVTKRGIYSG 355

Query: 387 AVGYFSFPDDKGRMNMDSAITIRSFFFKGKQGWL--QAGAGIVYDSVPEREYQETLNKLR 444
           + G  S   D      D  + IRS  +     +L  Q G  I Y S    EY+E L K  
Sbjct: 356 SFGCISAAGD-----FDFNVVIRSILYNAASNYLSFQVGGAITYQSNAVLEYEECLLKAS 410

Query: 445 ALFRSLE 451
           A+ + LE
Sbjct: 411 AILKVLE 417


Lambda     K      H
   0.319    0.137    0.392 

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: 467
Number of extensions: 20
Number of successful extensions: 3
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: 461
Length of database: 418
Length adjustment: 32
Effective length of query: 429
Effective length of database: 386
Effective search space:   165594
Effective search space used:   165594
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: 51 (24.3 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