GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpF in Sinorhizobium meliloti 1021

Align Aconitate-delta-isomerase 1; Itaconic acid/2-hydroxyparaconate biosynthesis cluster protein ADI1; EC 5.-.-.- (characterized)
to candidate SMc00497 SMc00497 tramsmembrane protein

Query= SwissProt::A0A0U2X0E4
         (443 letters)



>FitnessBrowser__Smeli:SMc00497
          Length = 352

 Score =  236 bits (603), Expect = 6e-67
 Identities = 136/319 (42%), Positives = 192/319 (60%), Gaps = 8/319 (2%)

Query: 11  RAGTSRGLYFLASDLPAEPSERDAALISIMGSGHPLQIDGMGGGNSLTSKVAIVSASTQR 70
           R GTS+G YFLA DLPA+  ERD  L+ IMGS  P QIDG+GG + LTSKVA+V AS  R
Sbjct: 12  RGGTSKGAYFLADDLPADAGERDRLLLRIMGSPDPRQIDGIGGADPLTSKVAVVRASA-R 70

Query: 71  SEFDVDYLFCQVGITERFVDTAPNCGNLMSGVAAFAIERGLVQPHPSDTTCLVRIFNLNS 130
            +FDVD+LF QV + +  V  + NCGN+++GV AFA+ERGLV+    +T   +RI+  N+
Sbjct: 71  PDFDVDFLFLQVFVDQALVSDSQNCGNILAGVGAFAVERGLVEAAEGETA--IRIYMENT 128

Query: 131 RQASELVIPVYNGR-VHYDDIDDMHMQRPSARVGLRFLDTVGSCTGKLLPTGNASDWIDG 189
            Q++   I   NGR V+  D     +  P+A V L F D  GS  G LLPTG+A++ I+G
Sbjct: 129 SQSAVARIRTANGRPVYAGDASIDGVPTPAAPVYLTFTDAAGSSCGALLPTGSAANEIEG 188

Query: 190 LKVSIIDSAVPVVFIRQHDVGITGSEAPATLNANTALLDRLERVRLEAGRRMGLGDVSGS 249
           +  ++ID+ +PVV +R  D G+TG E+   L AN ++  R+ER+RL AG  M LGDV   
Sbjct: 189 VACTLIDNGMPVVVMRAADFGLTGYESREELEANESVKARIERIRLAAGPLMNLGDVMKK 248

Query: 250 VVPKLSLIGPGTETTTFTARYFTPKACHNAHAVTGAICTAGAAYIDGSVVCEILSSRASA 309
            VPK++L+           R F P   H +  V GA+  A A  +  S      +S A  
Sbjct: 249 SVPKMTLVALPVNGGAIMTRSFIPHRVHASIGVFGALSVATACLLPNSPA----ASLAIL 304

Query: 310 CSASQRRISIEHPSGVLEV 328
               ++ +++EHP+G +E+
Sbjct: 305 PEGEEKTVAVEHPTGRMEI 323


Lambda     K      H
   0.318    0.133    0.389 

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: 368
Number of extensions: 13
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: 443
Length of database: 352
Length adjustment: 31
Effective length of query: 412
Effective length of database: 321
Effective search space:   132252
Effective search space used:   132252
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: 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