GapMind for catabolism of small carbon sources

 

Alignments for a candidate for uxuA in Dyella japonica UNC79MFTsu3.2

Align D-mannonate dehydratase; ManD; EC 4.2.1.8 (characterized)
to candidate N515DRAFT_1231 N515DRAFT_1231 galactonate dehydratase

Query= SwissProt::Q1NAJ2
         (403 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1231
          Length = 382

 Score =  189 bits (479), Expect = 2e-52
 Identities = 125/392 (31%), Positives = 201/392 (51%), Gaps = 36/392 (9%)

Query: 21  LKIMTDEGVYGLGDATLNGRELAVASYLTDHVIPCLIGRDAHRIEDLWQYLYKGAYWRRG 80
           L+I TD G+ G G+  + GR   VA+ + D +   LIG+D H IEDLW  +Y+  ++R G
Sbjct: 18  LRIDTDAGISGWGEPVVEGRAHTVAAAV-DELSDYLIGKDPHHIEDLWSVMYRAGFYRGG 76

Query: 81  PVTMTAIAAVDMALWDIKGKIAGLPVYQLLGGASREGVMVYGHANGTTIEDTVKVALDYQ 140
           P+ M+AIA +D ALWDIKGK  G PVY LLGG  R+ + VY    G    DT + A++  
Sbjct: 77  PILMSAIAGIDQALWDIKGKDLGRPVYDLLGGPVRDRIRVYSWIGGDRPADTARAAMEAV 136

Query: 141 AQGYKAIRLQCGVPGMASTYGVSKDKYFYEPADADLPTENIWNTSKYLRIVPELFKAARE 200
           A+G+ A+++             +++  + +  D            K  R++  + +A R+
Sbjct: 137 ARGFTAVKM-----------NATEEMQYVDSFD------------KVERVLANV-QAVRD 172

Query: 201 SLGWDVHLLHDIHHRLTPIEAGRLGQDLEPYRPFWLEDATPAENQEAFRLIRQHTTAPLA 260
           ++G  V L  D H R+    A  L ++LEPY+  ++E+   +E  E    +   + AP+A
Sbjct: 173 AVGPHVGLGLDFHGRVHKPMAKVLMRELEPYKLMFIEEPVLSEYLECIPELASISPAPIA 232

Query: 261 VGEIFNSIWDAKDLIQNQLIDYIRATVVHAGGITHLRRIAALADLYQIRTGCHGATDLSP 320
           +GE   S +D K +++   +D ++    HAGGIT  R+IAA+A+ Y +    H    L P
Sbjct: 233 LGERLYSRYDFKRVLETGGVDILQPDPSHAGGITETRKIAAMAEAYDVAIALH--CPLGP 290

Query: 321 VCMAAALHFDLSVPNFGIQEYMR--HMPETDAVFPH-----AYTFADGMMHPGDQPGLGV 373
           + +AA L  D    N  IQE     H   ++ +  +      + + DG +     PGLG+
Sbjct: 291 IALAANLQIDAVSHNAFIQEQSLGIHYNASNDLLDYVSDRSVFAYQDGYVTMPTGPGLGI 350

Query: 374 DIDEDLAA--GYEYKRAFLPVNRLEDGTMFNW 403
            ++E+  A    E  R   P+ R  DG++  W
Sbjct: 351 TVNEEYVAERAAEGHRWRNPLWRHADGSVAEW 382


Lambda     K      H
   0.322    0.139    0.438 

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: 430
Number of extensions: 23
Number of successful extensions: 4
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: 403
Length of database: 382
Length adjustment: 31
Effective length of query: 372
Effective length of database: 351
Effective search space:   130572
Effective search space used:   130572
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 Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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