GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Phaeobacter inhibens BS107

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate GFF1775 PGA1_c17990 D-malate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__Phaeo:GFF1775
          Length = 354

 Score =  215 bits (547), Expect = 2e-60
 Identities = 134/351 (38%), Positives = 197/351 (56%), Gaps = 24/351 (6%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETVEK 58
           YRI  I GDGIG EV+P  RRV++         +++ E +   E +   G  +PE+ +E+
Sbjct: 5   YRIAAIPGDGIGKEVLPVGRRVIDLVAQKHNFTVDWTEFDWSCERYHDTGRMMPEDGIEQ 64

Query: 59  ILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAK-----SRPVPG-SR 109
           + +  +   GA   P   VP     +G +  LRR LD YANVRP +     S P+ G   
Sbjct: 65  MKAFDSIYLGAVGFPG--VPDHVSLWGLLIPLRRELDQYANVRPVRLLKGISSPLAGRGA 122

Query: 110 PGVDLVIVRENTEGLYVEQERRYL-----DVAIADAVISKKASERIGRAALRIAEGRPRK 164
             +D++IVREN EG Y E   R       + AI +++++++ ++RI   A  +A+ R RK
Sbjct: 123 DDIDMIIVRENVEGEYSEIGGRVYQGTEHEAAIQESILTRRGTDRIMDYAFNVAKTRKRK 182

Query: 165 TLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTN 224
            +  A K+N +  T   + +     A+  P +      +D      V+ P+ FDV+V +N
Sbjct: 183 HVSSATKSNGIIHTMPFWDERFAAAAERHPAIGTAQFHIDIMTANFVLHPDWFDVVVASN 242

Query: 225 LLGDILSDLAAGLVGGLGLAPSGNI---GDTTAVFEPVHGSAPDIAGKGIANPTAAILSA 281
           L GDILSDL   + G +G+APS NI   G   ++FEPVHGSAPDIAGKG+ANP AA+ +A
Sbjct: 243 LFGDILSDLGPAVAGSIGIAPSANINPEGKYPSMFEPVHGSAPDIAGKGVANPVAAVWTA 302

Query: 282 AMMLDYLGEKEAAKRVEKAVDLVL-ERGPRTPDLGGDATTEAFTEAVVEAL 331
           AMML++LGE  AA  +E+A++  L     +T DLGG A T     A++ AL
Sbjct: 303 AMMLEHLGEANAAADIEQAIETSLASPDTKTRDLGGTADTAGSEAAILAAL 353


Lambda     K      H
   0.319    0.137    0.391 

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: 284
Number of extensions: 11
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: 334
Length of database: 354
Length adjustment: 29
Effective length of query: 305
Effective length of database: 325
Effective search space:    99125
Effective search space used:    99125
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 (21.7 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