GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Dethiosulfovibrio salsuginis USBA 82

Align isocitrate-homoisocitrate dehydrogenase (EC 1.1.1.286) (characterized)
to candidate WP_085545223.1 B9Y55_RS10015 isocitrate/isopropylmalate dehydrogenase family protein

Query= BRENDA::Q5JFV8
         (347 letters)



>NCBI__GCF_900177735.1:WP_085545223.1
          Length = 380

 Score =  171 bits (433), Expect = 3e-47
 Identities = 120/367 (32%), Positives = 173/367 (47%), Gaps = 50/367 (13%)

Query: 4   VAVIPGDGIGPEVIDGAVRVLKAVTG----RVRFEYYEGGVDVFQECGSPIREEDLEEIR 59
           +A I GDGIGPEV+    +   A        +R+  +  G   ++  G  + E  +EE+ 
Sbjct: 6   IAQIGGDGIGPEVVKQGRKAADAAMAGSGTELRWREFPWGAGHYRSTGEILPENAVEELS 65

Query: 60  RSDAVLFGATTTPFDLPGY--RSLILTLRKELGLYANLR-----------IIPDLRTGRE 106
             D++  GA   P   PG   R ++LTLR    +Y NLR           I      G +
Sbjct: 66  HCDSIYLGAIGDPSVKPGVLERGILLTLRFAFDMYVNLRPARAFPKVPIPIEGAAEKGID 125

Query: 107 IVIVRENSEGLYFGIGAVVNGR--------------------------AVDVRLITREGA 140
           +++VREN+E LY G+G   +G                           A+ + + T    
Sbjct: 126 LLVVRENTEDLYMGLGGTGDGEIDQIIEAKRGLYNLTGHVSMSTGHRMALQMGIATEPAV 185

Query: 141 ERIARFAVEQAKARGS-FITFVHKANVLTG-DKFFRRIVREVAGEEGVEVRDAIIDSFTI 198
            RI   A   A+ RG   I    KAN +     F+  I  + A  +G+ +    +D+   
Sbjct: 186 RRITATACGYARGRGERSILLATKANAMPHLYGFWEEIAADEAKGQGMAMETMNVDAMCY 245

Query: 199 KLVRNPWEHGVILSENLFGDILSDLATVHAGSIGIVPSGNYGDGIALFEPVHGSAPDIAG 258
             VR PWE G IL  NLFGDI+SDL     G +G+   GN GDGI +FEP+HGSAPDIAG
Sbjct: 246 HAVRRPWEFGTILCPNLFGDIVSDLFAGITGGLGVAAGGNQGDGIGMFEPIHGSAPDIAG 305

Query: 259 KGIANPIGAILSGAMLLDYL--GLDGSLIRAAVRGYVVNGE---LTPDMGGRARTEDVVR 313
              ANP+ AILS +++L  L  G   + I  AV  ++   +   L  +MGG+A TE++  
Sbjct: 306 TDSANPLAAILSASLMLRSLGEGKGATAIERAVETFLNESDQDRLPKEMGGQAGTEEIGD 365

Query: 314 GIIGEIE 320
            +   IE
Sbjct: 366 SVASIIE 372


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: 361
Number of extensions: 17
Number of successful extensions: 6
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: 380
Length adjustment: 29
Effective length of query: 318
Effective length of database: 351
Effective search space:   111618
Effective search space used:   111618
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