GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Nocardiopsis gilva YIM 90087

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_017621031.1 CDO52_RS22525 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_002263495.1:WP_017621031.1
          Length = 354

 Score =  201 bits (511), Expect = 2e-56
 Identities = 134/339 (39%), Positives = 186/339 (54%), Gaps = 25/339 (7%)

Query: 4   RICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETVEKI 59
           ++ +I GDGIG EV+    +VL A      +  +    E G + +   G ++P+   E++
Sbjct: 7   KLAVIPGDGIGPEVVAEGLKVLSAVASRHDIAFDTTTYELGAKRWHATGETLPDTVEEEL 66

Query: 60  LSCHATLFGAATSPTRKVPGFF---GAIRYLRRRLDLYANVRPAKSRP------VPGSRP 110
               A   GA   P+  VP      G +  LR     Y N+RP +  P         +  
Sbjct: 67  RGHEAIFLGAVGDPS--VPSGVLERGLLLRLRFNFSHYVNLRPVRLYPGVTCPLADAAPE 124

Query: 111 GVDLVIVRENTEGLY-----VEQERRYLDVAIADAVISKKASERIGRAALRIAEGRPRKT 165
            VD+++VRE TEG Y     V ++    ++A  D+V ++   ER+ R A   A  RPRK 
Sbjct: 125 DVDMLVVREGTEGPYAGMGGVLRKGTPGEIATQDSVNTRFGVERVVRYAFEKAAARPRKK 184

Query: 166 LHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTNL 225
           L + HK NVL     L+   V+EV  D+P V+V    VD   M  V +P+RFDV+VT NL
Sbjct: 185 LTLVHKDNVLTFAGELWQRVVREVGADYPQVSVDYCHVDAATMFFVTQPQRFDVVVTDNL 244

Query: 226 LGDILSDLAAGLVGGLGLAPSGNIGDTTA---VFEPVHGSAPDIAGKGIANPTAAILSAA 282
            GDI++DL A + GG+GLA SGNI    A   +FEPVHGSAPDIAG+  A+PTA +LSAA
Sbjct: 245 FGDIITDLGAAVAGGIGLAASGNINPENAFPSMFEPVHGSAPDIAGQSKADPTATVLSAA 304

Query: 283 MMLDYLGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTE 321
           +MLD+LG   AA++VE AV   LE   R  D G  +TT+
Sbjct: 305 IMLDHLGLGAAARQVENAVADDLE--ARAKDGGDRSTTQ 341


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: 336
Number of extensions: 16
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: 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 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