GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ligU in Cupriavidus basilensis 4G11

Align 4-oxalomesaconate tautomerase; Gallate degradation protein D; EC 5.3.2.8 (characterized)
to candidate RR42_RS11275 RR42_RS11275 3-methylitaconate isomerase

Query= SwissProt::Q88JY0
         (361 letters)



>FitnessBrowser__Cup4G11:RR42_RS11275
          Length = 396

 Score =  192 bits (489), Expect = 1e-53
 Identities = 137/395 (34%), Positives = 198/395 (50%), Gaps = 45/395 (11%)

Query: 3   QTRIPCLLMRGGTSKGAYFLHDDLP----APGPLRDRVLLAVMGSPD--ARQIDGIGGAD 56
           Q +IP   +RGGTSKG +F   DLP     PG  RD +L+ V+GSPD   +QIDG+G A 
Sbjct: 6   QIKIPATYIRGGTSKGVFFRLQDLPEAAQVPGAARDALLMRVIGSPDPYGKQIDGMGAAT 65

Query: 57  SLTSKVAIIRASQRDDADVDYLFAQVVVDEARVDYGQNCGNILAGVGPFALERGLVAAS- 115
           S TSK  I+  S + D DVDYLF QV +D+  VD+  NCGN+ A VGPFA+  GLV  S 
Sbjct: 66  SSTSKTVILSKSSKPDHDVDYLFGQVSIDQPFVDWSGNCGNLSAAVGPFAISAGLVDPSR 125

Query: 116 ---GASTPVRIFMENTGQIAVAQVPTADGQVEYAGDTRIDGVPGRAAALVVTFADVAG-- 170
                   VRI+  N G+  +  VP  +G V+  GD  +DGV   AA + + F D A   
Sbjct: 126 IPHNGVAIVRIWQANIGKTIIGHVPITNGAVQETGDFELDGVTFPAAEVQLEFMDPAAEE 185

Query: 171 -ASCGALLPTGNSRDCVE-----GVEVTCIDNGMPVVLLCAEDLGVTGYEPCETLEADSA 224
             + GA+ PTGN  D +E      ++ T I+ G+P + L AE +G  G E  + +  D  
Sbjct: 186 DGAGGAMFPTGNLIDDLEVPGVGTLKATMINAGIPTIFLDAESIGYKGTELQDAINGDPK 245

Query: 225 LKTRLEAIRLQLGPRMNL-----GDVSQRNVPKMCLLSAPRN----------GGTVN--T 267
                E IR     RM L        ++++ PK+  ++ P +           G V+   
Sbjct: 246 ALAMFETIRAHGAVRMGLIKHIDEAATRQHTPKVAFVAKPADYVASSGKQVAAGDVDLLV 305

Query: 268 RSFIPHRCHASIGVFGAVSVATACLIEGSVAQGLASTSGGDRQRLAVEHPSGEFTVEISL 327
           R+    + H ++    AV++ TA  I G++     +  GG R  +   HPSG  T+ +  
Sbjct: 306 RALSMGKLHHAMMGTAAVAIGTAAAITGTLVN--LAAGGGARNAVRFGHPSG--TLRVGA 361

Query: 328 EHGVIKGCGLV------RTARLLFDGVVCIGRDTW 356
           E   + G   V      R+AR+L +G V +  D +
Sbjct: 362 EASQVDGEWTVTKAIMSRSARVLMEGWVRVPGDAF 396


Lambda     K      H
   0.320    0.138    0.412 

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: 403
Number of extensions: 37
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: 361
Length of database: 396
Length adjustment: 30
Effective length of query: 331
Effective length of database: 366
Effective search space:   121146
Effective search space used:   121146
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: 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