GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Trichodesmium erythraeum IMS101

Align isocitrate-homoisocitrate dehydrogenase (EC 1.1.1.286) (characterized)
to candidate WP_011613717.1 TERY_RS21265 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5JFV8
         (347 letters)



>NCBI__GCF_000014265.1:WP_011613717.1
          Length = 360

 Score =  172 bits (435), Expect = 2e-47
 Identities = 125/312 (40%), Positives = 174/312 (55%), Gaps = 44/312 (14%)

Query: 3   RVAVIPGDGIGPEVIDGAVRVLKAVTGR--VRFEYYE---GGVDVFQECGSPIREEDLEE 57
           R+ ++PGDGIGPE++  AV VLK V  +  + FE+ E   GGV +    G P+ +E LE 
Sbjct: 5   RITLLPGDGIGPEIMAVAVDVLKVVGKQFNLEFEFQEAPIGGVAI-DATGEPLPKETLEM 63

Query: 58  IRRSDAVLFGATTTPFDLPGYR-----------SLILTLRKELGLYANLR---IIPDLRT 103
            R S+AVL  A      + GY+           + +L LR  LGL+ANLR   I P L  
Sbjct: 64  CRNSNAVLLAA------IGGYKWDNLPRHQRPETGLLGLRAGLGLFANLRPAKIFPQLID 117

Query: 104 ----------GREIVIVRENSEGLYFGIGAVV------NGRAVDVRLITREGAERIARFA 147
                     G +I++VRE + G+YFG    V        R V+    +    +RIA+  
Sbjct: 118 ASTLKREIVEGVDIMVVRELTGGVYFGTPKGVFETETKEKRGVNTMAYSESEIDRIAKVG 177

Query: 148 VEQAKARGSFITFVHKANVLTGDKFFRRIVREVAGE-EGVEVRDAIIDSFTIKLVRNPWE 206
            E A+ RG  +  V KANVL   +F+R  +  VA E + VE+    +D+  ++LVR P +
Sbjct: 178 FETAQKRGGKLCSVDKANVLEVSQFWRDRINLVAQEYQDVELSHLYVDNAAMQLVRFPKQ 237

Query: 207 HGVILSENLFGDILSDLATVHAGSIGIVPSGNYG-DGIALFEPVHGSAPDIAGKGIANPI 265
              I++ NLFGDILSD A +  GSIG++PS + G  G  +FEPVHGSAPDIAG+  ANP+
Sbjct: 238 FDTIVTGNLFGDILSDAAAMLTGSIGMLPSASLGASGPGVFEPVHGSAPDIAGQDKANPL 297

Query: 266 GAILSGAMLLDY 277
             +LS AM+L Y
Sbjct: 298 AQVLSVAMMLRY 309


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: 300
Number of extensions: 19
Number of successful extensions: 7
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: 360
Length adjustment: 29
Effective length of query: 318
Effective length of database: 331
Effective search space:   105258
Effective search space used:   105258
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 24 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