GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Herbaspirillum seropedicae SmR1

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate HSERO_RS16500 HSERO_RS16500 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__HerbieS:HSERO_RS16500
          Length = 356

 Score =  194 bits (492), Expect = 4e-54
 Identities = 142/367 (38%), Positives = 189/367 (51%), Gaps = 52/367 (14%)

Query: 4   RICLIEGDGIGHEVIPAARRVLEATGLPLEFVEAEAGWETFERRGTSVPEETVEKILSCH 63
           +I ++ GDGIG E++  A RVL A     E   A  G   +E  G  +P+ T++      
Sbjct: 2   KIAILPGDGIGPEIVNEAVRVLNALDEKFEMETAPVGGAGYEAHGHPLPDGTLKLAKEAD 61

Query: 64  ATLFGA-----------ATSPTRKVPGFFGAIRYLRRRLDLYANVRPAKSRPV------- 105
           A LFGA           A  P + + G       LR+ L L+AN RPA   P        
Sbjct: 62  AILFGAVGDWKYDKLERALRPEQAILG-------LRKHLQLFANFRPAICYPELTGASSL 114

Query: 106 -PGSRPGVDLVIVRENTEGLYVEQERRYLDVAIADAVISKKASERIGRAALRIAEGRPRK 164
            P     +D++IVRE    +Y  Q R      + +A        R G   +R +E   R+
Sbjct: 115 KPELVANLDILIVRELNGDIYFGQPR-----GMREAPDGPFKGAREGFDTMRYSEPEIRR 169

Query: 165 TLHIAH--------------KANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQL 210
             H+A               KANVL   Q  + D V EV K++P V +  + VDN AMQL
Sbjct: 170 IAHVAFQAAAKRGKRLCSVDKANVLETFQ-FWKDIVTEVGKEYPDVELSHMYVDNAAMQL 228

Query: 211 VMRPERFDVIVTTNLLGDILSDLAAGLVGGLGLAPSGNI-GDTTAVFEPVHGSAPDIAGK 269
           V  P+ FDVIVT N+ GDILSD AA L G +G+ PS ++  +   ++EP HGSAPDIAG+
Sbjct: 229 VKAPKNFDVIVTGNMFGDILSDAAAMLTGSIGMLPSASLDANNKGLYEPSHGSAPDIAGR 288

Query: 270 GIANPTAAILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFT---- 324
           GIANP A ILSAAMML + L + E A R+E AV  VL +G RT D+  +  T+  T    
Sbjct: 289 GIANPLATILSAAMMLRFSLNKAEQADRIENAVKKVLAQGLRTADIYEEGCTKVNTQQMG 348

Query: 325 EAVVEAL 331
           EAVV+AL
Sbjct: 349 EAVVKAL 355


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: 310
Number of extensions: 27
Number of successful extensions: 4
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: 356
Length adjustment: 29
Effective length of query: 305
Effective length of database: 327
Effective search space:    99735
Effective search space used:    99735
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