GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Bacteroides thetaiotaomicron VPI-5482

Align UDP-glucose 4-epimerase; Galactowaldenase; UDP-galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate 349906 BT0378 capsular polysaccharide biosynthesis protein capD (NCBI ptt file)

Query= SwissProt::Q9ZDJ5
         (341 letters)



>FitnessBrowser__Btheta:349906
          Length = 641

 Score =  146 bits (368), Expect = 2e-39
 Identities = 111/326 (34%), Positives = 161/326 (49%), Gaps = 31/326 (9%)

Query: 2   FVDKTLMITGGTGSFGNAVLSRFLKSNIINDIKEIRIFSRDEKKQEDMRIAL--NNSKLK 59
           F  K +++TG  GS G+ +  +  + NI    K++ +F   E    ++R+    N   L 
Sbjct: 294 FCGKVVLVTGAAGSIGSELCRQLAQMNI----KKLIMFDSAESPLHNVRLEFEKNYPDLD 349

Query: 60  FY--IGDVRNYQSIDDAM--HGVDYVFHAAALKQVPTCEFYPMEAINTNVLGAENVLSAA 115
           F   IGDVR  + +      +    +FHAAA K VP  E  P EA+  NV+G+  V   A
Sbjct: 350 FVPVIGDVRVKERLRMVFETYQPQIIFHAAAYKHVPLMEENPCEAVLVNVVGSRQVADMA 409

Query: 116 INNKVTKVIVLSTDKAVYPINAMGLSKALME----KLAIAKARMRSPGETILCVTRYGNV 171
           +     K+I++STDKAV P N MG SK L E     L  A    +  G T    TR+GNV
Sbjct: 410 VEYGAEKMIMVSTDKAVNPTNVMGCSKRLAEIYVQSLGCAIREGKVKGHTKFITTRFGNV 469

Query: 172 MASRGSVIPLFIHQIKQGKELTITEPSMTRFLMSLVDSVDLVLYAFEHGRQGDIFV-QKS 230
           + S GSVIP F  QI+ G  +T+T P + RF M++ ++  LV+ A   G   +IFV +  
Sbjct: 470 LGSNGSVIPRFKEQIENGGPVTVTHPDIIRFFMTIPEACRLVMEAATMGEGNEIFVFEMG 529

Query: 231 PASTIEVLAKALQEIFGSKNA----IRFIGTRHGEKHYESLVSSEDMAKADDLGGYYRIP 286
            A  I  LA  + E+ G +      I F G R GEK YE ++S ++            IP
Sbjct: 530 KAVKIVDLATRMIELAGYRPGEDIEIEFTGLRPGEKLYEEVLSDKENT----------IP 579

Query: 287 MDGRDLNYAKYFVTGEKKVALLDDYT 312
            + + +  AK  V   +   +LD YT
Sbjct: 580 TENKKIMIAK--VRHYEYTDILDTYT 603


Lambda     K      H
   0.319    0.135    0.373 

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: 438
Number of extensions: 22
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: 341
Length of database: 641
Length adjustment: 33
Effective length of query: 308
Effective length of database: 608
Effective search space:   187264
Effective search space used:   187264
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: 51 (24.3 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