GapMind for catabolism of small carbon sources

 

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

Align 4-oxalomesaconate tautomerase; Gallate degradation protein D; EC 5.3.2.8 (characterized)
to candidate N515DRAFT_0030 N515DRAFT_0030 2-methylaconitate cis-trans isomerase

Query= SwissProt::Q88JY0
         (361 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0030
          Length = 399

 Score =  203 bits (516), Expect = 7e-57
 Identities = 143/390 (36%), Positives = 206/390 (52%), Gaps = 49/390 (12%)

Query: 3   QTRIPCLLMRGGTSKGAYFLHDDLPA----PGPLRDRVLLAVMGSPD--ARQIDGIGGAD 56
           Q RIP   +RGGTSKG +F   DLPA    PG  RD +L  V+GSPD   +QIDG+GGA 
Sbjct: 11  QLRIPATYLRGGTSKGVFFRLQDLPAAAQVPGAARDALLQRVIGSPDPYGKQIDGMGGAT 70

Query: 57  SLTSKVAIIRASQRDDADVDYLFAQVVVDEARVDYGQNCGNILAGVGPFALERGLVAASG 116
           S TSK  I+  S R D DVDYLF QV +D+A VD+  NCGN+ A VGPFA+  GLV    
Sbjct: 71  SSTSKTVIVSRSSRADHDVDYLFGQVAIDKAFVDWSGNCGNLSAAVGPFAIANGLV--DP 128

Query: 117 ASTP------VRIFMENTGQIAVAQVPTADGQVEYAGDTRIDGVPGRAAALVVTFADVAG 170
           A  P      VRI+  N G+  +A+VP  DG V+  GD  +DGV   AA + + F D A 
Sbjct: 129 ARVPRDGIAIVRIWQANIGKTIIARVPITDGAVQETGDFELDGVTFPAAEVQLEFVDPAA 188

Query: 171 ---ASCGALLPTGNSRDCVE-----GVEVTCIDNGMPVVLLCAEDLGVTGYEPCETLEAD 222
               + GA+ PTG+  D +E      ++ T I+ G+P + + A  +G TG E  + + +D
Sbjct: 189 EEDGAGGAMFPTGHVVDDLEVPGVGTLKATMINAGIPTIFVEAAAIGYTGTELQDAINSD 248

Query: 223 SALKTRLEAIR----LQLGPRMNLGDVSQR-NVPKMCLLSAPRN----------GGTVN- 266
           +      E IR    L++G    L +++ R + PK+  ++ P +           G V+ 
Sbjct: 249 AKALAMFETIRAHGALRMGLIATLEEIATRQHTPKVAFVAGPADYLASSGKRVAAGDVDL 308

Query: 267 -TRSFIPHRCHASIGVFGAVSVATACLIEGSVAQGLASTSGGDRQRLAVEHPSGEFTVEI 325
             R+    + H ++    AV++ TA  I G++     +  GG+R  +   HPSG  T+ +
Sbjct: 309 LVRAMSMGKLHHAMMGTAAVAIGTAAAIPGTLVN--VAAGGGERHAVRFGHPSG--TLRV 364

Query: 326 SLEHGVIKGCGLV------RTARLLFDGVV 349
             E   + G   V      R+AR+L +G V
Sbjct: 365 GAEAAQVDGAWTVTKAVMSRSARVLMEGWV 394


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: 426
Number of extensions: 36
Number of successful extensions: 5
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: 399
Length adjustment: 30
Effective length of query: 331
Effective length of database: 369
Effective search space:   122139
Effective search space used:   122139
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.

Links

Downloads

Related tools

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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