GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ligU in Sinorhizobium meliloti 1021

Align (4E)-oxalomesaconate Delta-isomerase; OMA isomerase; 1,3-allylic isomerase LigU; EC 5.3.3.- (characterized)
to candidate SMc00497 SMc00497 tramsmembrane protein

Query= SwissProt::Q0KJL4
         (357 letters)



>FitnessBrowser__Smeli:SMc00497
          Length = 352

 Score =  465 bits (1197), Expect = e-136
 Identities = 231/348 (66%), Positives = 272/348 (78%)

Query: 9   DSAPCMWMRGGTSKGGYFLRADLPADTAARDAFLLAVMGSPDPRQIDGMGGADPLTSKVA 68
           D   CM MRGGTSKG YFL  DLPAD   RD  LL +MGSPDPRQIDG+GGADPLTSKVA
Sbjct: 4   DGIACMMMRGGTSKGAYFLADDLPADAGERDRLLLRIMGSPDPRQIDGIGGADPLTSKVA 63

Query: 69  VVSKSERPGIDVDYLFLQVFVDQAIVTDAQNCGNILAGVGPFAIERGLVAASGDETRVAI 128
           VV  S RP  DVD+LFLQVFVDQA+V+D+QNCGNILAGVG FA+ERGLV A+  ET + I
Sbjct: 64  VVRASARPDFDVDFLFLQVFVDQALVSDSQNCGNILAGVGAFAVERGLVEAAEGETAIRI 123

Query: 129 FMENTGQVAVATVRTPGGSVTYAGDAAIDGVPGTHAPIPTEFRDTAGSSCGALLPSGNAV 188
           +MENT Q AVA +RT  G   YAGDA+IDGVP   AP+   F D AGSSCGALLP+G+A 
Sbjct: 124 YMENTSQSAVARIRTANGRPVYAGDASIDGVPTPAAPVYLTFTDAAGSSCGALLPTGSAA 183

Query: 189 DVVNGLPVTLIDNGMPCVVMKAADVGITGYEDRDSLDANAELKAKIEAIRLAVGELMNLG 248
           + + G+  TLIDNGMP VVM+AAD G+TGYE R+ L+AN  +KA+IE IRLA G LMNLG
Sbjct: 184 NEIEGVACTLIDNGMPVVVMRAADFGLTGYESREELEANESVKARIERIRLAAGPLMNLG 243

Query: 249 DVTEKSVPKMMLVAPPRDGGAVCVRSFIPHRAHATIGVLGAVSVATACLIPGSPAAEVAV 308
           DV +KSVPKM LVA P +GGA+  RSFIPHR HA+IGV GA+SVATACL+P SPAA +A+
Sbjct: 244 DVMKKSVPKMTLVALPVNGGAIMTRSFIPHRVHASIGVFGALSVATACLLPNSPAASLAI 303

Query: 309 VPEGARKTLSIEHPTGEMSCVLEVDDAGNVVSAALLRTARKLMDGVVF 356
           +PEG  KT+++EHPTG M  +L +D+AG+V   + LRTARKL DG VF
Sbjct: 304 LPEGEEKTVAVEHPTGRMEILLRLDNAGSVEECSFLRTARKLFDGRVF 351


Lambda     K      H
   0.318    0.135    0.396 

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: 432
Number of extensions: 12
Number of successful extensions: 1
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: 357
Length of database: 352
Length adjustment: 29
Effective length of query: 328
Effective length of database: 323
Effective search space:   105944
Effective search space used:   105944
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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