GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Sulfuricurvum kujiense DSM 16994

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_013459847.1 SULKU_RS04995 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000183725.1:WP_013459847.1
          Length = 358

 Score =  220 bits (560), Expect = 5e-62
 Identities = 142/335 (42%), Positives = 200/335 (59%), Gaps = 24/335 (7%)

Query: 2   AYRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETVE 57
           +Y I LI+GDGIG E+I  A +VL+A      +   + EA  G   ++  G  +P+ET++
Sbjct: 3   SYNIALIKGDGIGPEIIDEAVKVLDAVAACENIEFNYQEALMGGCAYDVTGDPLPQETID 62

Query: 58  KILSCHATLFGAA------TSPTRKVPGFFGAIRYLRRRLDLYANVRPAK--------SR 103
             LS +A LFGA       T P  K P   G +R+ R+ L ++AN+RPA         S 
Sbjct: 63  ISLSSNAVLFGAIGGQKWDTLPREKRPES-GLLRF-RKELGVFANLRPANVYDELVNASS 120

Query: 104 PVPGSRPGVDLVIVRENTEGLYV-EQERRYLDVAIADAVISKKASERIGRAALRIAEGRP 162
             P    GVDL++VRE   G+Y  E + R  +      V ++   ERI   A +IA  R 
Sbjct: 121 LKPEIVKGVDLMVVRELIGGIYFGEPKGRDENKGWNTMVYTRPEIERIAHVAFKIAMERS 180

Query: 163 RKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVT 222
           +K   +  KANVL ++Q L+ + V+EVAK++P V +  + VDN AMQL+  P++FDVI+T
Sbjct: 181 KKVCSV-DKANVLDVSQ-LWREVVEEVAKEYPEVELSHMYVDNAAMQLIRDPKQFDVILT 238

Query: 223 TNLLGDILSDLAAGLVGGLGLAPSGNIGDTTAVFEPVHGSAPDIAGKGIANPTAAILSAA 282
            N+ GDILSD A+ L G +GL PS ++G +  V+EP+HGSAPDIAG+GIANP A I SA+
Sbjct: 239 GNIFGDILSDEASMLSGSIGLLPSASVGSSIGVYEPIHGSAPDIAGQGIANPIATIASAS 298

Query: 283 MMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGG 316
           MML + LGE  AA R++  +   L  G RT D+ G
Sbjct: 299 MMLRFALGENRAADRIDYGIKQALAEGYRTKDIAG 333


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: 283
Number of extensions: 9
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: 358
Length adjustment: 29
Effective length of query: 305
Effective length of database: 329
Effective search space:   100345
Effective search space used:   100345
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