GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Caulobacter crescentus NA1000

Align UDP-glucose 4-epimerase; Galactowaldenase; UDP-galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate CCNA_00233 CCNA_00233 UDP-N-acetylglucosamine 4,6-dehydratase

Query= SwissProt::Q9ZDJ5
         (341 letters)



>FitnessBrowser__Caulo:CCNA_00233
          Length = 345

 Score =  220 bits (560), Expect = 5e-62
 Identities = 131/320 (40%), Positives = 188/320 (58%), Gaps = 16/320 (5%)

Query: 5   KTLMITGGTGSFGNAVLSRFLKSNIINDIKEIRIFSRDEKKQEDMRIALNN-------SK 57
           K +++TGGTGSFG   +   L+     D +++ ++SRDE KQ DM+I L         +K
Sbjct: 14  KVILVTGGTGSFGRRFIETVLRRY---DPRKVIVYSRDELKQSDMQIELREQFDEATVAK 70

Query: 58  LKFYIGDVRNYQSIDDAMHGVDYVFHAAALKQVPTCEFYPMEAINTNVLGAENVLSAAIN 117
           ++F++GDVR+ + +  A+ GVD V HAAALKQVP  E+ P E I+TNVLGAENV+ A++ 
Sbjct: 71  MRFFLGDVRDRERLTLALRGVDIVIHAAALKQVPAAEYNPSECIHTNVLGAENVVWASLA 130

Query: 118 NKVTKVIVLSTDKAVYPINAMGLSKALMEKLAIAKARMRSPGETILCVTRYGNVMASRGS 177
           N V +V+ LSTDKA  P N  G +K   +K  +A   +     T  CV RYGNV+ SRGS
Sbjct: 131 NAVKQVVALSTDKACNPTNLYGATKLASDKTFVAANNLSGDIGTRFCVVRYGNVVGSRGS 190

Query: 178 VIPLFIHQIKQG-KELTITEPSMTRFLMSLVDSVDLVLYAFEHGRQGDIFVQKSPASTIE 236
           V+PL+   + QG  EL +T+P MTRF ++L + VD VL +    R G+IFV K P+  + 
Sbjct: 191 VVPLYRRLLSQGATELPVTDPRMTRFWITLNEGVDFVLSSLTMMRGGEIFVPKIPSMAMP 250

Query: 237 VLAKALQEIFGSKNAIRFIGTRHGEKHYESLVSSEDMAKADDLGGYYRIPMDGRDLNYAK 296
            L KA+     S  A++ IG R GEK +E ++S++D     +    Y I  +  +     
Sbjct: 251 DLVKAM----SSTAAMKVIGIRPGEKLHEIMISADDARSTVEFDDRYAIEPNFAEFGREP 306

Query: 297 YFVT-GEKKVALLDDYTSHN 315
           Y  + G K VA    Y+S N
Sbjct: 307 YAASDGAKPVAEDFSYSSDN 326


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: 293
Number of extensions: 13
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: 341
Length of database: 345
Length adjustment: 29
Effective length of query: 312
Effective length of database: 316
Effective search space:    98592
Effective search space used:    98592
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: 49 (23.5 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