GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Sinorhizobium meliloti 1021

Align isocitrate-homoisocitrate dehydrogenase (EC 1.1.1.286) (characterized)
to candidate SMa1846 SMa1846 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5JFV8
         (347 letters)



>FitnessBrowser__Smeli:SMa1846
          Length = 347

 Score =  175 bits (444), Expect = 1e-48
 Identities = 124/346 (35%), Positives = 180/346 (52%), Gaps = 29/346 (8%)

Query: 2   YRVAVIPGDGIGPEVIDGAVRVLKAVTGRVRFEY----YEGGVDVFQECGSPIREEDLEE 57
           Y +A+IPGDGIG +V D A +VL  V     F      +      ++E G+ +  + +E 
Sbjct: 4   YSIALIPGDGIGQDVTDAAWQVLSTVARHSGFTLTGTSFPWSCAFYKETGAMMPADGIEA 63

Query: 58  IRRSDAVLFGATTTPFDLP---GYRSLILTLRKELGLYANLRII--------PDLRTGRE 106
           +R  DA+L G+   P ++P       L+L +RK    YAN+R          P   +  +
Sbjct: 64  LRPFDAILLGSVGWPAEVPDSISLHGLLLPIRKAFVQYANIRPHRLLSGVEGPLKASDFD 123

Query: 107 IVIVRENSEGLYFGIGAVVNGR-----AVDVRLITREGAERIARFAVEQAKARGSFITFV 161
           I+ VREN+EG Y G G  V+       AV+  + TR G ERI RFA EQA+ R   +  V
Sbjct: 124 ILCVRENTEGEYSGAGGRVHQGTADEVAVETSIFTRAGVERILRFAFEQARQRRGKLASV 183

Query: 162 HKANVLTGDK-FFRRIVREVAGE-EGVEVRDAIIDSFTIKLVRNPWEHGVILSENLFGDI 219
            K+N       F+  + R++A E   VEV    ID+   ++V  P    V+++ NLFGDI
Sbjct: 184 TKSNAQKHSMVFWDEVTRQLADEYPDVEVTSYHIDAMAARVVMAPESLDVVVASNLFGDI 243

Query: 220 LSDLATVHAGSIGIVPSGNYG---DGIALFEPVHGSAPDIAGKGIANPIGAILSGAMLLD 276
           L+DL     G +G   S N        ++FEPVHGSAPDIA  GIANPI AI SGAM+L+
Sbjct: 244 LTDLGAAIQGGLGFAASANINPDRSAPSMFEPVHGSAPDIAHLGIANPIAAIWSGAMMLE 303

Query: 277 YLG--LDGSLIRAAVRGYVVNGELTPDMGGRARTEDVVRGIIGEIE 320
           +LG      +I AA+    + G  T  + G+ RT  +   ++  ++
Sbjct: 304 HLGEREAAGMIMAALERTTIRGIGT--VPGKDRTRSITAAVLAALD 347


Lambda     K      H
   0.321    0.143    0.411 

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: 281
Number of extensions: 12
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: 347
Length of database: 347
Length adjustment: 29
Effective length of query: 318
Effective length of database: 318
Effective search space:   101124
Effective search space used:   101124
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